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Polycythemia Due To Stress Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polycythemia Due To Stress in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
polycythemia; polycythemia vera Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycythemia; polycythemia vera in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myeloproliferative disorders; polycythemia; polycythemia vera; thrombocythemia, essential; thrombocytosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myeloproliferative disorders; polycythemia; polycythemia vera; thrombocythemia, essential; thrombocytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycythemia vera(c15.378.190.636.753)/enzymology; polycythemia(c15.378.738)/enzymology Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycythemia vera(c15.378.190.636.753)/enzymology; polycythemia(c15.378.738)/enzymology in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
stress polycythemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease stress polycythemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
Stress Polycythemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stress Polycythemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stress polycythemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Stress polycythemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Polycythemia Due To Erythropoietin Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polycythemia Due To Erythropoietin in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polycythemia Due To Excess Erythopoetin Production Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polycythemia Due To Excess Erythopoetin Production in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polycythemia Due To Fall In Plasma Volume Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polycythemia Due To Fall In Plasma Volume in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polycythemia Due To High Altitude Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polycythemia Due To High Altitude in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary familial polycythemia due to EPO receptor mutation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Primary familial polycythemia due to EPO receptor mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Evasion of Oxidative Stress Induced Senescence Due to Defective p16INK4A binding to CDK4 Gene Setproteins participating in the Evasion of Oxidative Stress Induced Senescence Due to Defective p16INK4A binding to CDK4 pathway from the Reactome Pathways 2024 dataset. |
Evasion of Oxidative Stress Induced Senescence Due to Defective p16INK4A binding to CDK4 and CDK6 Gene Setproteins participating in the Evasion of Oxidative Stress Induced Senescence Due to Defective p16INK4A binding to CDK4 and CDK6 pathway from the Reactome Pathways 2024 dataset. |
Evasion of Oxidative Stress Induced Senescence Due to p14ARF Defects Gene Setproteins participating in the Evasion of Oxidative Stress Induced Senescence Due to p14ARF Defects pathway from the Reactome Pathways 2024 dataset. |
Evasion of Oxidative Stress Induced Senescence Due to p16INK4A Defects Gene Setproteins participating in the Evasion of Oxidative Stress Induced Senescence Due to p16INK4A Defects pathway from the Reactome Pathways 2024 dataset. |
THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN from the curated CTD Gene-Disease Associations dataset. |
Hypermanganesemia with dystonia, polycythemia and cirrhosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypermanganesemia with dystonia, polycythemia and cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Polycythemia Vera Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Polycythemia Vera from the curated CTD Gene-Disease Associations dataset. |
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypermanganesemia with Dystonia Polycythemia and Cirrhosis from the curated CTD Gene-Disease Associations dataset. |
Polycythemia, primary familial and congenital Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Polycythemia, primary familial and congenital from the curated CTD Gene-Disease Associations dataset. |
Polycythemia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Polycythemia from the curated CTD Gene-Disease Associations dataset. |
polycythemia vera Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease polycythemia vera from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
primary polycythemia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease primary polycythemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
polycythemia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease polycythemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
polycythemia vera Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease polycythemia vera in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
primary polycythemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary polycythemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
acquired polycythemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease acquired polycythemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
polycythemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease polycythemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lymphoma; myeloproliferative disorders; polycythemia vera; thrombocythemia, essential Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lymphoma; myeloproliferative disorders; polycythemia vera; thrombocythemia, essential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycythemia vera; thrombocythemia, essential; thrombocythemia, hemorrhagic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycythemia vera; thrombocythemia, essential; thrombocythemia, hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myeloproliferative disorders; polycythemia vera; thrombocythemia, essential; thrombocythemia, hemorrhagic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myeloproliferative disorders; polycythemia vera; thrombocythemia, essential; thrombocythemia, hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
neovascularization, pathologic; polycythemia vera; thrombocythemia, essential; thrombocythemia, hemorrhagic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease neovascularization, pathologic; polycythemia vera; thrombocythemia, essential; thrombocythemia, hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycythemia vera; thrombocythemia, essential; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycythemia vera; thrombocythemia, essential; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myeloproliferative disorders; philadelphia chromosome; polycythemia vera; primary myelofibrosis; thrombocythemia, essential; thrombocythemia, hemorrhagic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myeloproliferative disorders; philadelphia chromosome; polycythemia vera; primary myelofibrosis; thrombocythemia, essential; thrombocythemia, hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chuvash-type congenital polycythemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chuvash-type congenital polycythemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycythemia vera; thrombocythemia, hemorrhagic; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycythemia vera; thrombocythemia, hemorrhagic; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial mediterranean fever; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid; leukemia, myeloid, acute; myelodysplastic syndromes; myeloid leukemia; polycythemia vera; preleukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid; leukemia, myeloid, acute; myelodysplastic syndromes; myeloid leukemia; polycythemia vera; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myeloproliferative disorders; polycythemia vera; primary myelofibrosis; thrombocythemia, essential Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myeloproliferative disorders; polycythemia vera; primary myelofibrosis; thrombocythemia, essential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anoxia; blood coagulation disorders, inherited; heart defects, congenital; infection; polycythemia; postoperative complications; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anoxia; blood coagulation disorders, inherited; heart defects, congenital; infection; polycythemia; postoperative complications; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, pulmonary; polycythemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, pulmonary; polycythemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycythemia vera; primary myelofibrosis; thrombocythemia, essential Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycythemia vera; primary myelofibrosis; thrombocythemia, essential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hematologic neoplasms; polycythemia vera; thrombocythemia, essential Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hematologic neoplasms; polycythemia vera; thrombocythemia, essential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; polycythemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; polycythemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycythemia vera Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycythemia vera in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; cardiovascular diseases; polycythemia vera; recurrence; thrombocythemia, hemorrhagic; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; cardiovascular diseases; polycythemia vera; recurrence; thrombocythemia, hemorrhagic; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blast crisis; blast phase; polycythemia vera; primary myelofibrosis; thrombocythemia, essential; thrombocythemia, hemorrhagic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blast crisis; blast phase; polycythemia vera; primary myelofibrosis; thrombocythemia, essential; thrombocythemia, hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycythemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycythemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycythemia vera; thrombocythemia, essential Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycythemia vera; thrombocythemia, essential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myeloproliferative disorders; polycythemia vera Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myeloproliferative disorders; polycythemia vera in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
genetic diseases, inborn; polycythemia vera; thrombocythemia, essential Gene SetFrom GAD Gene-Disease Associations genes associated with the disease genetic diseases, inborn; polycythemia vera; thrombocythemia, essential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycythemia vera; primary myelofibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycythemia vera; primary myelofibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, myelogenous, chronic, bcr-abl positive; myelodysplastic syndromes; myeloproliferative disorders; polycythemia vera; precursor cell lymphoblastic leukemia-lymphoma; thrombocythemia, essential Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, myelogenous, chronic, bcr-abl positive; myelodysplastic syndromes; myeloproliferative disorders; polycythemia vera; precursor cell lymphoblastic leukemia-lymphoma; thrombocythemia, essential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cell transformation, neoplastic; leucocytosis; leukemia; leukocytosis; polycythemia vera; primary myelofibrosis; vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cell transformation, neoplastic; leucocytosis; leukemia; leukocytosis; polycythemia vera; primary myelofibrosis; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia, iron-deficiency; polycythemia vera Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; polycythemia vera in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hemochromatosis; polycythemia vera Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hemochromatosis; polycythemia vera in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myeloproliferative disorders; polycythemia vera; thrombocythemia, essential Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myeloproliferative disorders; polycythemia vera; thrombocythemia, essential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
congenital polycythemia. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease congenital polycythemia. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycythemia Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term polycythemia in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
polycythemia vera Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease polycythemia vera in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
polycythemia Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease polycythemia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
polycythemia Gene SetFrom HPO Gene-Disease Associations genes associated with the polycythemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Polycythemia Vera Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Polycythemia Vera phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Polycythemia Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Polycythemia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
polycythemia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the polycythemia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
polycythemia vera Gene SetFrom OMIM Gene-Disease Associations genes associated with the polycythemia vera phenotype from the curated OMIM Gene-Disease Associations dataset. |
hypermanganesemia with dystonia, polycythemia, and cirrhosis Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypermanganesemia with dystonia, polycythemia, and cirrhosis phenotype from the curated OMIM Gene-Disease Associations dataset. |
Polycythemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polycythemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polycythemia Vera Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polycythemia Vera in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Polycythemia Gene SetFrom 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. |
Familial Polycythemia Vera Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Polycythemia Vera in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
polycythemia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the polycythemia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Primary polycythemia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Primary polycythemia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Polycythemia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Polycythemia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Polycythemia vera Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Polycythemia vera from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Primary polycythemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary polycythemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Polycythemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Polycythemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Polycythemia vera Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Polycythemia vera in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Physiological polycythemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Physiological polycythemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired polycythemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired polycythemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Chuvash polycythemia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Chuvash polycythemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Acquired polycythemia vera Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Acquired polycythemia vera phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Polycythemia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Polycythemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
rho-selective guanine exchange factor akap13 mediates stress fiber formation Gene SetFrom Biocarta Pathways proteins participating in the rho-selective guanine exchange factor akap13 mediates stress fiber formation pathway from the Biocarta Pathways dataset. |
stress induction of hsp regulation Gene SetFrom Biocarta Pathways proteins participating in the stress induction of hsp regulation pathway from the Biocarta Pathways dataset. |
tnf/stress related signaling Gene SetFrom Biocarta Pathways proteins participating in the tnf/stress related signaling pathway from the Biocarta Pathways dataset. |
oxidative stress induced gene expression via nrf2 Gene SetFrom Biocarta Pathways proteins participating in the oxidative stress induced gene expression via nrf2 pathway from the Biocarta Pathways dataset. |
stress fiber Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the stress fiber cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
cytoplasmic stress granule Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the cytoplasmic stress granule cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
nuclear stress granule Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the nuclear stress granule cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
stress fiber Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the stress fiber cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
nuclear stress granule Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the nuclear stress granule cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
cytoplasmic stress granule Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cytoplasmic stress granule cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
FOXO3-PCAF complex, oxidative stress stimulated Gene Setproteins in the FOXO3-PCAF complex, oxidative stress stimulated protein complex from the CORUM Protein Complexes dataset. |
FOXO3-SIRT1 complex, oxidative stress stimulated Gene Setproteins in the FOXO3-SIRT1 complex, oxidative stress stimulated protein complex from the CORUM Protein Complexes dataset. |
FOXO3-TP53 complex, oxidative stress stimulated Gene Setproteins in the FOXO3-TP53 complex, oxidative stress stimulated protein complex from the CORUM Protein Complexes dataset. |
Stress Disorders, Post-Traumatic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Stress Disorders, Post-Traumatic from the curated CTD Gene-Disease Associations dataset. |
Heat Stress Disorders Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Heat Stress Disorders from the curated CTD Gene-Disease Associations dataset. |
female stress incontinence Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease female stress incontinence in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
post-traumatic stress disorder Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease post-traumatic stress disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
acute stress disorder Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease acute stress disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
social stress Gene SetFrom GAD Gene-Disease Associations genes associated with the disease social stress in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
stroke; oxidative stress Gene SetFrom GAD Gene-Disease Associations genes associated with the disease stroke; oxidative stress in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood pressure, oxidative stress levels in blood Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood pressure, oxidative stress levels in blood in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
stress Gene SetFrom GAD Gene-Disease Associations genes associated with the disease stress in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
posttraumatic stress disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease posttraumatic stress disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
impaired exercise stress response Gene SetFrom GAD Gene-Disease Associations genes associated with the disease impaired exercise stress response in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
post-traumatic stress disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease post-traumatic stress disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
stress; chronic disease burden Gene SetFrom GAD Gene-Disease Associations genes associated with the disease stress; chronic disease burden in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fractures, stress Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fractures, stress in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
psychosocial stress. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease psychosocial stress. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood flow; vascular response; oxidative stress; nitirc oxide production; nitric oxide-mediated effect on resistance vessels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood flow; vascular response; oxidative stress; nitirc oxide production; nitric oxide-mediated effect on resistance vessels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
heat stress disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease heat stress disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcoholism; stress Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcoholism; stress in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
responses to psychosocial stress Gene SetFrom GAD Gene-Disease Associations genes associated with the disease responses to psychosocial stress in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
occupational stress Gene SetFrom GAD Gene-Disease Associations genes associated with the disease occupational stress in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
urinary incontinence, stress; uterine prolapse Gene SetFrom GAD Gene-Disease Associations genes associated with the disease urinary incontinence, stress; uterine prolapse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
posttraumatic stress disorder. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease posttraumatic stress disorder. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
femoral neck fractures; fractures, stress Gene SetFrom GAD Gene-Disease Associations genes associated with the disease femoral neck fractures; fractures, stress in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
stress (tako-tsubo) cardiomyopathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease stress (tako-tsubo) cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adhd ; post-traumatic stress disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adhd ; post-traumatic stress disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
oxidative stress Gene SetFrom GAD Gene-Disease Associations genes associated with the disease oxidative stress in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
stress Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term stress in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
PTSD - Post-traumatic stress disorder_Peripheral blood mononuclear cell_GSE860 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during PTSD - Post-traumatic stress disorder_Peripheral blood mononuclear cell_GSE860 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
positive regulation of cardiac muscle hypertrophy in response to stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of cardiac muscle hypertrophy in response to stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular response to oxidative stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular response to oxidative stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular response to osmotic stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular response to osmotic stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of transcription from rna polymerase ii promoter in response to endoplasmic reticulum stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of transcription from rna polymerase ii promoter in response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of oxidative stress-induced cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
intrinsic apoptotic signaling pathway in response to endoplasmic reticulum stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the intrinsic apoptotic signaling pathway in response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
cardiac muscle hypertrophy in response to stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cardiac muscle hypertrophy in response to stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of cellular response to oxidative stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of cellular response to oxidative stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of translational initiation in response to stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of translational initiation in response to stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of translational initiation in response to stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of translational initiation in response to stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of translational initiation in response to stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of translational initiation in response to stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of oxidative stress-induced intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of oxidative stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of response to stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of response to stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
stress granule assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the stress granule assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
muscle hypertrophy in response to stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the muscle hypertrophy in response to stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of intrinsic apoptotic signaling pathway in response to osmotic stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of intrinsic apoptotic signaling pathway in response to osmotic stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to osmotic stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to osmotic stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of stress-activated mapk cascade Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of stress-activated mapk cascade biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to oxidative stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to oxidative stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
intrinsic apoptotic signaling pathway in response to osmotic stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the intrinsic apoptotic signaling pathway in response to osmotic stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
stress-activated mapk cascade Gene SetFrom GO Biological Process Annotations 2015 genes participating in the stress-activated mapk cascade biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of oxidative stress-induced neuron death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of oxidative stress-induced neuron death biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to salt stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to salt stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of cellular response to oxidative stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of cellular response to oxidative stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of mrna stability involved in response to stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of mrna stability involved in response to stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of oxidative stress-induced intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of oxidative stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to isolation stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to isolation stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of transcription from rna polymerase ii promoter in response to stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of transcription from rna polymerase ii promoter in response to stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of translation in response to stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of translation in response to stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of oxidative stress-induced cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of oxidative stress-induced neuron death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of oxidative stress-induced neuron death biological process from the curated GO Biological Process Annotations 2015 dataset. |
detection of oxidative stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the detection of oxidative stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of stress fiber assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of stress fiber assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
stress-activated protein kinase signaling cascade Gene SetFrom GO Biological Process Annotations 2015 genes participating in the stress-activated protein kinase signaling cascade biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of oxidative stress-induced intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of oxidative stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
stress fiber assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the stress fiber assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of dna-templated transcription in response to stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of dna-templated transcription in response to stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
stress-induced mitochondrial fusion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the stress-induced mitochondrial fusion biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of translation in response to stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of translation in response to stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular response to salt stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular response to salt stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
stress-induced premature senescence Gene SetFrom GO Biological Process Annotations 2015 genes participating in the stress-induced premature senescence biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to nitrosative stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to nitrosative stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of translation in response to stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of translation in response to stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of response to endoplasmic reticulum stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular response to fluid shear stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular response to fluid shear stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of stress-activated protein kinase signaling cascade Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of stress-activated protein kinase signaling cascade biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of stress-activated mapk cascade Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of stress-activated mapk cascade biological process from the curated GO Biological Process Annotations 2015 dataset. |
stress granule disassembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the stress granule disassembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of endoplasmic reticulum stress-induced neuron intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of endoplasmic reticulum stress-induced neuron intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to laminar fluid shear stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to laminar fluid shear stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of cardiac muscle hypertrophy in response to stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of cardiac muscle hypertrophy in response to stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of transcription from rna polymerase ii promoter in response to endoplasmic reticulum stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of transcription from rna polymerase ii promoter in response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of intrinsic apoptotic signaling pathway in response to osmotic stress by p53 class mediator Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of intrinsic apoptotic signaling pathway in response to osmotic stress by p53 class mediator biological process from the curated GO Biological Process Annotations 2015 dataset. |
multicellular organismal response to stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the multicellular organismal response to stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of oxidative stress-induced cell death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to fluid shear stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to fluid shear stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of stress fiber assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of stress fiber assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of stress fiber assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of stress fiber assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of transcription from rna polymerase ii promoter in response to oxidative stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of transcription from rna polymerase ii promoter in response to oxidative stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
age-dependent response to oxidative stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the age-dependent response to oxidative stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
oxidative stress-induced premature senescence Gene SetFrom GO Biological Process Annotations 2015 genes participating in the oxidative stress-induced premature senescence biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of intrinsic apoptotic signaling pathway in response to osmotic stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of intrinsic apoptotic signaling pathway in response to osmotic stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of intrinsic apoptotic signaling pathway in response to osmotic stress by p53 class mediator Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of intrinsic apoptotic signaling pathway in response to osmotic stress by p53 class mediator biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular stress response to acidic ph Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular stress response to acidic ph biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of response to oxidative stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of response to oxidative stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of endoplasmic reticulum stress-induced neuron intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of endoplasmic reticulum stress-induced neuron intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of response to osmotic stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of response to osmotic stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of transcription from rna polymerase ii promoter in response to stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of transcription from rna polymerase ii promoter in response to stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
intrinsic apoptotic signaling pathway in response to oxidative stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the intrinsic apoptotic signaling pathway in response to oxidative stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
mrna export from nucleus in response to heat stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the mrna export from nucleus in response to heat stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to immobilization stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to immobilization stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of oxidative stress-induced neuron death Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of oxidative stress-induced neuron death biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of transcription from rna polymerase ii promoter in response to stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of transcription from rna polymerase ii promoter in response to stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular response to stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular response to stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of cellular response to oxidative stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of cellular response to oxidative stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular response to laminar fluid shear stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular response to laminar fluid shear stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of cardiac muscle hypertrophy in response to stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of cardiac muscle hypertrophy in response to stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of stress-activated protein kinase signaling cascade Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of stress-activated protein kinase signaling cascade biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of response to oxidative stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of response to oxidative stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of transcription from rna polymerase ii promoter in response to oxidative stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of transcription from rna polymerase ii promoter in response to oxidative stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of stress-activated protein kinase signaling cascade Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of stress-activated protein kinase signaling cascade biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of stress-activated mapk cascade Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of stress-activated mapk cascade biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to endoplasmic reticulum stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of cellular response to stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of cellular response to stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of response to oxidative stress Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of response to oxidative stress biological process from the curated GO Biological Process Annotations 2015 dataset. |
stress fiber Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the stress fiber cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
cytoplasmic stress granule Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the cytoplasmic stress granule cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
nuclear stress granule Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the nuclear stress granule cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
Post-traumatic stress disorder (asjusted for relatedness) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Post-traumatic stress disorder (asjusted for relatedness) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Post-traumatic stress disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Post-traumatic stress disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
post-traumatic stress disorder Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease post-traumatic stress disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
apneic episodes precipitated by illness, fatigue, stress Gene SetFrom HPO Gene-Disease Associations genes associated with the apneic episodes precipitated by illness, fatigue, stress phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased red cell hemolysis by shear stress Gene SetFrom HPO Gene-Disease Associations genes associated with the increased red cell hemolysis by shear stress phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
stress/infection-induced lactic acidosis Gene SetFrom HPO Gene-Disease Associations genes associated with the stress/infection-induced lactic acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Stress Disorders, Traumatic, Acute Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Stress Disorders, Traumatic, Acute phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Stress, Psychological Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Stress, Psychological phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Stress Disorders, Post-Traumatic Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Stress Disorders, Post-Traumatic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Urinary Incontinence, Stress Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Urinary Incontinence, Stress phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Stress Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Stress phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Fractures, Stress Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Fractures, Stress phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Stress Disorders, Traumatic Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Stress Disorders, Traumatic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Heat Stress Disorders Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Heat Stress Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Stress-associated endoplasmic reticulum protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Stress-associated endoplasmic reticulum protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Stress-activated map kinase interacting 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Stress-activated map kinase interacting 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Oxidative stress-induced growth inhibitor 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Oxidative stress-induced growth inhibitor 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Oxidative stress-induced growth inhibitor 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Oxidative stress-induced growth inhibitor 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
increased response of heart to induced stress Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased response of heart to induced stress phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased response of heart to induced stress Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased response of heart to induced stress phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased cellular sensitivity to oxidative stress Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased cellular sensitivity to oxidative stress phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal response to stress-induced hyperthermia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal response to stress-induced hyperthermia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased response to stress-induced hyperthermia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased response to stress-induced hyperthermia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased cellular sensitivity to oxidative stress Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased cellular sensitivity to oxidative stress phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
altered response of heart to induced stress Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the altered response of heart to induced stress phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
oxidative stress Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the oxidative stress phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased response to stress-induced hyperthermia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased response to stress-induced hyperthermia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Oxidative stress response Gene SetFrom PANTHER Pathways proteins participating in the Oxidative stress response pathway from the PANTHER Pathways dataset. |
stress Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term stress in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
DNA Damage/Telomere Stress Induced Senescence Gene Setproteins participating in the DNA Damage/Telomere Stress Induced Senescence pathway from the Reactome Pathways dataset. |
Cellular responses to stress Gene Setproteins participating in the Cellular responses to stress pathway from the Reactome Pathways dataset. |
Activation of ATR in response to replication stress Gene Setproteins participating in the Activation of ATR in response to replication stress pathway from the Reactome Pathways dataset. |
Oxidative Stress Induced Senescence Gene Setproteins participating in the Oxidative Stress Induced Senescence pathway from the Reactome Pathways dataset. |
Cellular response to heat stress Gene Setproteins participating in the Cellular response to heat stress pathway from the Reactome Pathways dataset. |
FAS pathway and Stress induction of HSP regulation(Homo sapiens) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the FAS pathway and Stress induction of HSP regulation(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset. |
Oxidative Stress(Mus musculus) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the Oxidative Stress(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset. |
Oxidative Stress(Homo sapiens) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the Oxidative Stress(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset. |
FAS pathway and Stress induction of HSP regulation(Mus musculus) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the FAS pathway and Stress induction of HSP regulation(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset. |
Urinary Stress Incontinence Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Urinary Stress Incontinence in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stress, Psychological Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stress, Psychological in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Post-Traumatic Stress Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Post-Traumatic Stress Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Acute Reactions To Stress Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Acute Reactions To Stress in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Social Stress Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Social Stress in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stress Induced Hyperglycaemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stress Induced Hyperglycaemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stress Ulcer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stress Ulcer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stress Ulcer Of Stomach Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stress Ulcer Of Stomach in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Water Stress Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Water Stress in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stress-Induced Polymorphic Ventricular Tachycardia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stress-Induced Polymorphic Ventricular Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Reaction To Severe Stress, And Adjustment Disorders Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Reaction To Severe Stress, And Adjustment Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chronic Post-Traumatic Stress Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chronic Post-Traumatic Stress Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stress/Infection-Induced Lactic Acidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stress/Infection-Induced Lactic Acidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stress Related Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stress Related Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Female Stress Incontinence Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Female Stress Incontinence in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stress Induced Cardiomyopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stress Induced Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Heat Stress Disorders Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Heat Stress Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Symptoms Of Stress Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Symptoms Of Stress in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Cardiac Exercise Stress Test Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Cardiac Exercise Stress Test in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Emotional Stress Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Emotional Stress in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Red Cell Hemolysis By Shear Stress Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Red Cell Hemolysis By Shear Stress in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
intrinsic apoptotic signaling pathway in response to endoplasmic reticulum stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intrinsic apoptotic signaling pathway in response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
stress fiber assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the stress fiber assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
oxidative stress-induced premature senescence Gene SetFrom GO Biological Process Annotations 2023 genes participating in the oxidative stress-induced premature senescence biological process from the curated GO Biological Process Annotations 2023 dataset. |
response to endoplasmic reticulum stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of stress-activated MAPK cascade Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of stress-activated MAPK cascade biological process from the curated GO Biological Process Annotations 2023 dataset. |
stress granule assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the stress granule assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of translation in response to endoplasmic reticulum stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of translation in response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
cellular response to osmotic stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cellular response to osmotic stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein localization to cytoplasmic stress granule Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein localization to cytoplasmic stress granule biological process from the curated GO Biological Process Annotations 2023 dataset. |
cellular response to oxidative stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cellular response to oxidative stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of stress fiber assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of stress fiber assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
stress-activated MAPK cascade Gene SetFrom GO Biological Process Annotations 2023 genes participating in the stress-activated MAPK cascade biological process from the curated GO Biological Process Annotations 2023 dataset. |
response to laminar fluid shear stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the response to laminar fluid shear stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
response to salt stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the response to salt stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
cardiac muscle hypertrophy in response to stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cardiac muscle hypertrophy in response to stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
cellular response to fluid shear stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cellular response to fluid shear stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of stress fiber assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of stress fiber assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
intrinsic apoptotic signaling pathway in response to oxidative stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intrinsic apoptotic signaling pathway in response to oxidative stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of transcription from RNA polymerase II promoter in response to endoplasmic reticulum stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of transcription from RNA polymerase II promoter in response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of oxidative stress-induced intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of oxidative stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
cellular response to laminar fluid shear stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cellular response to laminar fluid shear stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of DNA-templated transcription in response to stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of DNA-templated transcription in response to stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of stress-activated protein kinase signaling cascade Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of stress-activated protein kinase signaling cascade biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of endoplasmic reticulum stress-induced eIF2 alpha phosphorylation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of endoplasmic reticulum stress-induced eIF2 alpha phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset. |
stress granule disassembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the stress granule disassembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of cellular response to stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of cellular response to stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
integrated stress response signaling Gene SetFrom GO Biological Process Annotations 2023 genes participating in the integrated stress response signaling biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of cellular response to oxidative stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of cellular response to oxidative stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of oxidative stress-induced cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of response to endoplasmic reticulum stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of stress-activated MAPK cascade Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of stress-activated MAPK cascade biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of stress fiber assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of stress fiber assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of response to oxidative stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of response to oxidative stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of endoplasmic reticulum stress-induced eIF2 alpha dephosphorylation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of endoplasmic reticulum stress-induced eIF2 alpha dephosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of response to endoplasmic reticulum stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
stress-activated protein kinase signaling cascade Gene SetFrom GO Biological Process Annotations 2023 genes participating in the stress-activated protein kinase signaling cascade biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of cardiac muscle hypertrophy in response to stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of cardiac muscle hypertrophy in response to stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of oxidative stress-induced intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of oxidative stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of transcription from RNA polymerase II promoter in response to stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of transcription from RNA polymerase II promoter in response to stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of stress-activated MAPK cascade Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of stress-activated MAPK cascade biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of intrinsic apoptotic signaling pathway in response to osmotic stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of intrinsic apoptotic signaling pathway in response to osmotic stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of cardiac muscle hypertrophy in response to stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of cardiac muscle hypertrophy in response to stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of transcription from RNA polymerase II promoter in response to stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of transcription from RNA polymerase II promoter in response to stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of translation in response to endoplasmic reticulum stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of translation in response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of transcription from RNA polymerase II promoter in response to endoplasmic reticulum stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of transcription from RNA polymerase II promoter in response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of oxidative stress-induced intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of oxidative stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of response to osmotic stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of response to osmotic stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of oxidative stress-induced cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of transcription from RNA polymerase II promoter in response to oxidative stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of transcription from RNA polymerase II promoter in response to oxidative stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
mRNA export from nucleus in response to heat stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the mRNA export from nucleus in response to heat stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of translation in response to stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of translation in response to stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
trehalose metabolism in response to stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the trehalose metabolism in response to stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
cellular stress response to acid chemical Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cellular stress response to acid chemical biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of transcription from RNA polymerase II promoter in response to stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of transcription from RNA polymerase II promoter in response to stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of transcription from RNA polymerase II promoter in response to oxidative stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of transcription from RNA polymerase II promoter in response to oxidative stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of oxidative stress-induced neuron death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of oxidative stress-induced neuron death biological process from the curated GO Biological Process Annotations 2023 dataset. |
cellular response to chemical stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cellular response to chemical stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
cellular response to salt stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cellular response to salt stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of nitrosative stress-induced intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of nitrosative stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of endoplasmic reticulum stress-induced neuron intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of endoplasmic reticulum stress-induced neuron intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of response to endoplasmic reticulum stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
stress-induced premature senescence Gene SetFrom GO Biological Process Annotations 2023 genes participating in the stress-induced premature senescence biological process from the curated GO Biological Process Annotations 2023 dataset. |
endoplasmic reticulum stress-induced pre-emptive quality control Gene SetFrom GO Biological Process Annotations 2023 genes participating in the endoplasmic reticulum stress-induced pre-emptive quality control biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of translation in response to endoplasmic reticulum stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of translation in response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of translation initiation in response to endoplasmic reticulum stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of translation initiation in response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of stress granule assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of stress granule assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of cellular response to osmotic stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of cellular response to osmotic stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
cellular response to nitrosative stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cellular response to nitrosative stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of cardiac muscle hypertrophy in response to stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of cardiac muscle hypertrophy in response to stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of stress granule assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of stress granule assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
detection of oxidative stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the detection of oxidative stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of response to oxidative stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of response to oxidative stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
intrinsic apoptotic signaling pathway in response to osmotic stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intrinsic apoptotic signaling pathway in response to osmotic stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of translation in response to stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of translation in response to stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
stress-induced mitochondrial fusion Gene SetFrom GO Biological Process Annotations 2023 genes participating in the stress-induced mitochondrial fusion biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of mRNA stability involved in response to stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of mRNA stability involved in response to stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
eiF2alpha phosphorylation in response to endoplasmic reticulum stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the eiF2alpha phosphorylation in response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of endoplasmic reticulum stress-induced eIF2 alpha phosphorylation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of endoplasmic reticulum stress-induced eIF2 alpha phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of response to oxidative stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of response to oxidative stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of cytoplasmic translational initiation in response to stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of cytoplasmic translational initiation in response to stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
cellular stress response to acidic pH Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cellular stress response to acidic pH biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of translation in response to stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of translation in response to stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of stress-activated protein kinase signaling cascade Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of stress-activated protein kinase signaling cascade biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of response to stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of response to stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of oxidative stress-induced cell death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of translational initiation in response to stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of translational initiation in response to stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of endoplasmic reticulum stress-induced eIF2 alpha dephosphorylation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of endoplasmic reticulum stress-induced eIF2 alpha dephosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of response to salt stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of response to salt stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of stress-activated protein kinase signaling cascade Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of stress-activated protein kinase signaling cascade biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of intrinsic apoptotic signaling pathway in response to osmotic stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of intrinsic apoptotic signaling pathway in response to osmotic stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of oxidative stress-induced neuron death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of oxidative stress-induced neuron death biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of nitrosative stress-induced intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of nitrosative stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of oxidative stress-induced neuron death Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of oxidative stress-induced neuron death biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of translation initiation in response to endoplasmic reticulum stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of translation initiation in response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of stress granule assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of stress granule assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of cytoplasmic translation in response to stress Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of cytoplasmic translation in response to stress biological process from the curated GO Biological Process Annotations 2023 dataset. |
cytoplasmic stress granule Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the cytoplasmic stress granule cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
nuclear stress granule Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the nuclear stress granule cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
NR3C1-34362910-WISTARRAT-HIPPOCAMPUS-STRESS Gene SetFrom ChEA Transcription Factor Targets 2022 target genes of the NR3C1-34362910-WISTARRAT-HIPPOCAMPUS-STRESS transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset. |
NR3C2-34362910-WISTARRAT-HIPPOCAMPUS-STRESS Gene SetFrom ChEA Transcription Factor Targets 2022 target genes of the NR3C2-34362910-WISTARRAT-HIPPOCAMPUS-STRESS transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset. |
oxidative stress Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the oxidative stress phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal response of heart to induced stress Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal response of heart to induced stress phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased response of heart to induced stress Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased response of heart to induced stress phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased cellular sensitivity to oxidative stress Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased cellular sensitivity to oxidative stress phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased response of heart to induced stress Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased response of heart to induced stress phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased cellular sensitivity to oxidative stress Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cellular sensitivity to oxidative stress phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal stress erythropoiesis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal stress erythropoiesis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal response to stress-induced hyperthermia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal response to stress-induced hyperthermia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased response to stress-induced hyperthermia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased response to stress-induced hyperthermia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased endoplasmic reticulum stress Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased endoplasmic reticulum stress phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased response to stress-induced hyperthermia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased response to stress-induced hyperthermia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal endoplasmic reticulum stress Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal endoplasmic reticulum stress phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Human - Lung v2 (HLCA) - L3 - SM activated stress response Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Lung v2 (HLCA) - L3 - SM activated stress response cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Lung v2 (HLCA) - Finest - SM activated stress response Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Lung v2 (HLCA) - Finest - SM activated stress response cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Adipose multilineage-differentiating stress-enduring cell_Adipose tissue_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Adipose multilineage-differentiating stress-enduring cell_Adipose tissue_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Fas ligand pathway and stress induction of heat shock proteins Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Fas ligand pathway and stress induction of heat shock proteins pathway from the WikiPathways Pathways 2024 dataset. |
Interactions between LOXL4 and oxidative stress pathway Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Interactions between LOXL4 and oxidative stress pathway pathway from the WikiPathways Pathways 2024 dataset. |
Oxidative stress response Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Oxidative stress response pathway from the WikiPathways Pathways 2024 dataset. |
Endoplasmic reticulum stress response in coronavirus infection Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Endoplasmic reticulum stress response in coronavirus infection pathway from the WikiPathways Pathways 2024 dataset. |
SARS CoV 2 mitochondrial chronic oxidative stress and endothelial dysfunction Gene SetFrom WikiPathways Pathways 2024 proteins participating in the SARS CoV 2 mitochondrial chronic oxidative stress and endothelial dysfunction pathway from the WikiPathways Pathways 2024 dataset. |
ATF4 activates genes in response to endoplasmic reticulum stress Gene Setproteins participating in the ATF4 activates genes in response to endoplasmic reticulum stress pathway from the Reactome Pathways 2024 dataset. |
Activation of ATR in response to replication stress Gene Setproteins participating in the Activation of ATR in response to replication stress pathway from the Reactome Pathways 2024 dataset. |
Cellular response to chemical stress Gene Setproteins participating in the Cellular response to chemical stress pathway from the Reactome Pathways 2024 dataset. |
Cellular response to heat stress Gene Setproteins participating in the Cellular response to heat stress pathway from the Reactome Pathways 2024 dataset. |
Cellular response to mitochondrial stress Gene Setproteins participating in the Cellular response to mitochondrial stress pathway from the Reactome Pathways 2024 dataset. |
Cellular responses to stress Gene Setproteins participating in the Cellular responses to stress pathway from the Reactome Pathways 2024 dataset. |
DNA Damage/Telomere Stress Induced Senescence Gene Setproteins participating in the DNA Damage/Telomere Stress Induced Senescence pathway from the Reactome Pathways 2024 dataset. |
Diseases of cellular response to stress Gene Setproteins participating in the Diseases of cellular response to stress pathway from the Reactome Pathways 2024 dataset. |
FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes Gene Setproteins participating in the FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes pathway from the Reactome Pathways 2024 dataset. |
High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR in endothelial cells Gene Setproteins participating in the High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR in endothelial cells pathway from the Reactome Pathways 2024 dataset. |
NFE2L2 regulating ER-stress associated genes Gene Setproteins participating in the NFE2L2 regulating ER-stress associated genes pathway from the Reactome Pathways 2024 dataset. |
Oxidative Stress Induced Senescence Gene Setproteins participating in the Oxidative Stress Induced Senescence pathway from the Reactome Pathways 2024 dataset. |
Response of endothelial cells to shear stress Gene Setproteins participating in the Response of endothelial cells to shear stress pathway from the Reactome Pathways 2024 dataset. |
Turbulent (oscillatory, disturbed) flow shear stress activates signaling by PIEZO1 and integrins in endothelial cells Gene Setproteins participating in the Turbulent (oscillatory, disturbed) flow shear stress activates signaling by PIEZO1 and integrins in endothelial cells pathway from the Reactome Pathways 2024 dataset. |
intrinsic apoptotic signaling pathway in response to endoplasmic reticulum stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intrinsic apoptotic signaling pathway in response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of translation in response to stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of translation in response to stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
stress fiber assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the stress fiber assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
oxidative stress-induced premature senescence Gene SetFrom GO Biological Process Annotations 2025 genes participating in the oxidative stress-induced premature senescence biological process from the curated GO Biological Process Annotations 2025 dataset. |
response to endoplasmic reticulum stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of stress-activated MAPK cascade Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of stress-activated MAPK cascade biological process from the curated GO Biological Process Annotations 2025 dataset. |
cellular response to oxidative stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cellular response to oxidative stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
stress granule assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the stress granule assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of translation in response to endoplasmic reticulum stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of translation in response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
cellular response to osmotic stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cellular response to osmotic stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
protein localization to cytoplasmic stress granule Gene SetFrom GO Biological Process Annotations 2025 genes participating in the protein localization to cytoplasmic stress granule biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of stress fiber assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of stress fiber assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
stress-activated MAPK cascade Gene SetFrom GO Biological Process Annotations 2025 genes participating in the stress-activated MAPK cascade biological process from the curated GO Biological Process Annotations 2025 dataset. |
response to laminar fluid shear stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the response to laminar fluid shear stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
response to salt stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the response to salt stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
cardiac muscle hypertrophy in response to stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cardiac muscle hypertrophy in response to stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
cellular response to fluid shear stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cellular response to fluid shear stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
vascular endothelial cell response to laminar fluid shear stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the vascular endothelial cell response to laminar fluid shear stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of stress fiber assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of stress fiber assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
intrinsic apoptotic signaling pathway in response to oxidative stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intrinsic apoptotic signaling pathway in response to oxidative stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of oxidative stress-induced intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of oxidative stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
cellular response to laminar fluid shear stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cellular response to laminar fluid shear stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
stress granule disassembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the stress granule disassembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of cellular response to stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of cellular response to stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
integrated stress response signaling Gene SetFrom GO Biological Process Annotations 2025 genes participating in the integrated stress response signaling biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of cellular response to oxidative stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of cellular response to oxidative stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of response to endoplasmic reticulum stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of stress-activated MAPK cascade Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of stress-activated MAPK cascade biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of stress fiber assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of stress fiber assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of response to oxidative stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of response to oxidative stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of response to oxidative stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of response to oxidative stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of response to oxidative stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of response to oxidative stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of translation in response to endoplasmic reticulum stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of translation in response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of translational initiation in response to stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of translational initiation in response to stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of response to endoplasmic reticulum stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
stress-activated protein kinase signaling cascade Gene SetFrom GO Biological Process Annotations 2025 genes participating in the stress-activated protein kinase signaling cascade biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of cardiac muscle hypertrophy in response to stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of cardiac muscle hypertrophy in response to stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of oxidative stress-induced intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of oxidative stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
vascular endothelial cell response to oscillatory fluid shear stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the vascular endothelial cell response to oscillatory fluid shear stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of stress-activated MAPK cascade Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of stress-activated MAPK cascade biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of intrinsic apoptotic signaling pathway in response to osmotic stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of intrinsic apoptotic signaling pathway in response to osmotic stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of cardiac muscle hypertrophy in response to stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of cardiac muscle hypertrophy in response to stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of translation in response to stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of translation in response to stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of endoplasmic reticulum stress-induced neuron intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of endoplasmic reticulum stress-induced neuron intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of response to endoplasmic reticulum stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of oxidative stress-induced intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of oxidative stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
mRNA export from nucleus in response to heat stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the mRNA export from nucleus in response to heat stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of translation in response to stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of translation in response to stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
cellular stress response to acid chemical Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cellular stress response to acid chemical biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of translation initiation in response to endoplasmic reticulum stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of translation initiation in response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
cellular response to chemical stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cellular response to chemical stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
cellular response to salt stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cellular response to salt stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of translation in response to oxidative stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of translation in response to oxidative stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of nitrosative stress-induced intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of nitrosative stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of cardiac muscle hypertrophy in response to stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of cardiac muscle hypertrophy in response to stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
endoplasmic reticulum stress-induced pre-emptive quality control Gene SetFrom GO Biological Process Annotations 2025 genes participating in the endoplasmic reticulum stress-induced pre-emptive quality control biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of translation in response to endoplasmic reticulum stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of translation in response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of translation initiation in response to endoplasmic reticulum stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of translation initiation in response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of endoplasmic reticulum stress-induced eIF2 alpha phosphorylation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of endoplasmic reticulum stress-induced eIF2 alpha phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of stress granule assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of stress granule assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of cellular response to osmotic stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of cellular response to osmotic stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
cellular response to nitrosative stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cellular response to nitrosative stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of stress granule assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of stress granule assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of response to osmotic stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of response to osmotic stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
detection of oxidative stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the detection of oxidative stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
intrinsic apoptotic signaling pathway in response to osmotic stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intrinsic apoptotic signaling pathway in response to osmotic stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
neuron intrinsic apoptotic signaling pathway in response to oxidative stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the neuron intrinsic apoptotic signaling pathway in response to oxidative stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
stress-induced mitochondrial fusion Gene SetFrom GO Biological Process Annotations 2025 genes participating in the stress-induced mitochondrial fusion biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of stress-activated protein kinase signaling cascade Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of stress-activated protein kinase signaling cascade biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of mRNA stability involved in response to stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of mRNA stability involved in response to stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
eiF2alpha phosphorylation in response to endoplasmic reticulum stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the eiF2alpha phosphorylation in response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of endoplasmic reticulum stress-induced eIF2 alpha phosphorylation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of endoplasmic reticulum stress-induced eIF2 alpha phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of cytoplasmic translational initiation in response to stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of cytoplasmic translational initiation in response to stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of stress-activated protein kinase signaling cascade Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of stress-activated protein kinase signaling cascade biological process from the curated GO Biological Process Annotations 2025 dataset. |
vascular endothelial cell response to fluid shear stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the vascular endothelial cell response to fluid shear stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of response to stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of response to stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of stress-activated protein kinase signaling cascade Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of stress-activated protein kinase signaling cascade biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of response to salt stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of response to salt stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
cellular response to oscillatory fluid shear stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cellular response to oscillatory fluid shear stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of intrinsic apoptotic signaling pathway in response to osmotic stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of intrinsic apoptotic signaling pathway in response to osmotic stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of translation in response to oxidative stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of translation in response to oxidative stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of nitrosative stress-induced intrinsic apoptotic signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of nitrosative stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of stress granule assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of stress granule assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of cytoplasmic translation in response to stress Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of cytoplasmic translation in response to stress biological process from the curated GO Biological Process Annotations 2025 dataset. |
cytoplasmic stress granule Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the cytoplasmic stress granule cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
nuclear stress granule Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the nuclear stress granule cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
post-traumatic stress disorder Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease post-traumatic stress disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
post-traumatic stress disorder Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease post-traumatic stress disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acute stress disorder Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acute stress disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
stress-induced childhood-onset neurodegeneration with variable ataxia and seizures Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease stress-induced childhood-onset neurodegeneration with variable ataxia and seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Female stress incontinence Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Female stress incontinence in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Nuclear stress granule Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Nuclear stress granule cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Stress fiber Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Stress fiber cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Cytoplasmic stress granule Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Cytoplasmic stress granule cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Cytoplasmic stress granule Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Cytoplasmic stress granule cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Stress fiber Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Stress fiber cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Nuclear stress granule Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Nuclear stress granule cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Stress urinary incontinence Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Stress urinary incontinence phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Protein folding and stress response regulation Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Protein folding and stress response regulation assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Regulation of gene expression and signal transduction in immune and stress responses Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of gene expression and signal transduction in immune and stress responses assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Regulation of gene expression and cellular stress response Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of gene expression and cellular stress response assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Regulation of cellular stress responses and metal ion homeostasis Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of cellular stress responses and metal ion homeostasis assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Regulation of p53-mediated cellular stress response Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of p53-mediated cellular stress response assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
DNA Repair and Cellular Stress Response Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising DNA Repair and Cellular Stress Response assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Stress response complex Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Stress response complex assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
spontaneous preterm birth x maternal stress interaction (1df) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the spontaneous preterm birth x maternal stress interaction (1df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Post-traumatic stress disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Post-traumatic stress disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Post traumatic stress disorder symptom count in trauma-exposed individuals Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Post traumatic stress disorder symptom count in trauma-exposed individuals phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Stress urinary incontinence Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Stress urinary incontinence phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Rumination (response to stress) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Rumination (response to stress) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Brooding (response to stress) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Brooding (response to stress) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Reflection (response to stress) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Reflection (response to stress) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Hip circumference (psychosocial stress interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hip circumference (psychosocial stress interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Psychological resilience (outcome-based) in high deployment stress exposure Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Psychological resilience (outcome-based) in high deployment stress exposure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Post-traumatic stress disorder (asjusted for relatedness) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Post-traumatic stress disorder (asjusted for relatedness) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Post-traumatic stress disorder symptoms in trauma-exposed soldiers Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Post-traumatic stress disorder symptoms in trauma-exposed soldiers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Anxiety and stress-related disorders Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Anxiety and stress-related disorders phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Stress-related disorders Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Stress-related disorders phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Anxiety and stress-related disorders (excluding adjustment disorder) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Anxiety and stress-related disorders (excluding adjustment disorder) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Anxiety and stress-related disorders (excluding co-morbid schizophrenia) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Anxiety and stress-related disorders (excluding co-morbid schizophrenia) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Anxiety and stress-related disorders (including obsessive-compulsive disorder) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Anxiety and stress-related disorders (including obsessive-compulsive disorder) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Anxiety and stress-related disorders (psychiatric co-morbidity weighting design) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Anxiety and stress-related disorders (psychiatric co-morbidity weighting design) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Anxiety and stress-related disorders (psychiatric co-morbidity covariate model) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Anxiety and stress-related disorders (psychiatric co-morbidity covariate model) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Stress sensitivity (neuroticism score x major depressive disorder status interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Stress sensitivity (neuroticism score x major depressive disorder status interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Fluid shear stress and atherosclerosis Gene SetFrom KEGG Pathways 2026 proteins participating in the Fluid shear stress and atherosclerosis pathway from the KEGG Pathways 2026 dataset. |
Carbonic anhydrase va deficiency, hyperammonemia due to Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Carbonic anhydrase va deficiency, hyperammonemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
SCID due to ADA deficiency, delayed onset Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the SCID due to ADA deficiency, delayed onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thrombophilia due to protein S deficiency, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thrombophilia due to protein S deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe combined immunodeficiency due to ADA deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe combined immunodeficiency due to ADA deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
HNSHA due to aldolase A deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the HNSHA due to aldolase A deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ehlers-Danlos-like syndrome due to tenascin-X deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos-like syndrome due to tenascin-X deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gaucher disease, atypical, due to saposin C deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gaucher disease, atypical, due to saposin C deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Disordered steroidogenesis due to cytochrome p450 oxidoreductase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Disordered steroidogenesis due to cytochrome p450 oxidoreductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Megaloblastic anemia due to inborn errors of metabolism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Megaloblastic anemia due to inborn errors of metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hemolytic anemia due to hexokinase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hemolytic anemia due to hexokinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Leigh syndrome due to mitochondrial complex I deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Leigh syndrome due to mitochondrial complex I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Homocysteinemia due to MTHFR deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Homocysteinemia due to MTHFR deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Immunodeficiency due to ficolin 3 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Immunodeficiency due to ficolin 3 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thrombophilia due to activated protein C resistance Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thrombophilia due to activated protein C resistance phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypermethioninemia due to adenosine kinase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypermethioninemia due to adenosine kinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pseudohermaphroditism, female, with hypokalemia, due to glucocorticoid resistance Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pseudohermaphroditism, female, with hypokalemia, due to glucocorticoid resistance phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thrombophilia due to thrombomodulin defect Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thrombophilia due to thrombomodulin defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Muscular dystrophy, congenital, due to ITGA7 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Muscular dystrophy, congenital, due to ITGA7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Immunodeficiency due to defect in cd3-zeta Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Immunodeficiency due to defect in cd3-zeta phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Homocystinuria due to MTHFR deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Homocystinuria due to MTHFR deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Leigh syndrome due to mitochondrial complex II deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Leigh syndrome due to mitochondrial complex II deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Complement component 4, partial deficiency of, due to dysfunctional c1 inhibitor Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Complement component 4, partial deficiency of, due to dysfunctional c1 inhibitor phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy due to partial LAMA2 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy due to partial LAMA2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Megaloblastic anemia due to dihydrofolate reductase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Megaloblastic anemia due to dihydrofolate reductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Obesity, severe, due to leptin deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Obesity, severe, due to leptin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Adenylate kinase deficiency, hemolytic anemia due to Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Adenylate kinase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thrombophilia, hereditary, due to protein C deficiency, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thrombophilia, hereditary, due to protein C deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperphenylalaninemia, bh4-deficient, a, due to partial pts deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperphenylalaninemia, bh4-deficient, a, due to partial pts deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Immune dysfunction with T-cell inactivation due to calcium entry defect 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Immune dysfunction with T-cell inactivation due to calcium entry defect 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Immune dysfunction with T-cell inactivation due to calcium entry defect 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Immune dysfunction with T-cell inactivation due to calcium entry defect 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Congenital adrenal hyperplasia due to 21 hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset. |
Thrombophilia, X-Linked, Due To Factor Ix Defect Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Thrombophilia, X-Linked, Due To Factor Ix Defect from the curated CTD Gene-Disease Associations dataset. |
HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset. |
Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency from the curated CTD Gene-Disease Associations dataset. |
Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type from the curated CTD Gene-Disease Associations dataset. |
Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to from the curated CTD Gene-Disease Associations dataset. |
Congenital thrombotic disease, due to Protein C deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Congenital thrombotic disease, due to Protein C deficiency from the curated CTD Gene-Disease Associations dataset. |
ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO from the curated CTD Gene-Disease Associations dataset. |
Adenylate Kinase Deficiency, Hemolytic Anemia Due To Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Adenylate Kinase Deficiency, Hemolytic Anemia Due To from the curated CTD Gene-Disease Associations dataset. |
Neurodegeneration Due To Cerebral Folate Transport Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neurodegeneration Due To Cerebral Folate Transport Deficiency from the curated CTD Gene-Disease Associations dataset. |
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset. |
Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency from the curated CTD Gene-Disease Associations dataset. |
Severe combined immunodeficiency due to adenosine deaminase deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Severe combined immunodeficiency due to adenosine deaminase deficiency from the curated CTD Gene-Disease Associations dataset. |
Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency from the curated CTD Gene-Disease Associations dataset. |
Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to from the curated CTD Gene-Disease Associations dataset. |
METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT from the curated CTD Gene-Disease Associations dataset. |
Pseudohyperkalemia, Familial, 2, due to Red Cell Leak Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pseudohyperkalemia, Familial, 2, due to Red Cell Leak from the curated CTD Gene-Disease Associations dataset. |
Krabbe Disease, Atypical, due to Saposin A Deficiency Gene SetFrom 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. |
HEPATIC FIBROSIS, SEVERE, SUSCEPTIBILITY TO, DUE TO SCHISTOSOMA MANSONI INFECTION Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HEPATIC FIBROSIS, SEVERE, SUSCEPTIBILITY TO, DUE TO SCHISTOSOMA MANSONI INFECTION from the curated CTD Gene-Disease Associations dataset. |
Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency from the curated CTD Gene-Disease Associations dataset. |
Gaucher Disease, Atypical, Due To Saposin C Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Gaucher Disease, Atypical, Due To Saposin C Deficiency from the curated CTD Gene-Disease Associations dataset. |
Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to from the curated CTD Gene-Disease Associations dataset. |
Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations from the curated CTD Gene-Disease Associations dataset. |
Thrombophilia Due To Elevated Histidine-Rich Glycoprotein Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Thrombophilia Due To Elevated Histidine-Rich Glycoprotein from the curated CTD Gene-Disease Associations dataset. |
Thrombophilia due to Activated Protein C Resistance Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Thrombophilia due to Activated Protein C Resistance from the curated CTD Gene-Disease Associations dataset. |
THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset. |
Immunodeficiency due to Defect in CD3-Zeta Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Immunodeficiency due to Defect in CD3-Zeta from the curated CTD Gene-Disease Associations dataset. |
Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset. |
Metachromatic Leukodystrophy due to Saposin B Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Metachromatic Leukodystrophy due to Saposin B Deficiency from the curated CTD Gene-Disease Associations dataset. |
Immunodeficiency due to Defect in MAPBP-Interacting Protein Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Immunodeficiency due to Defect in MAPBP-Interacting Protein from the curated CTD Gene-Disease Associations dataset. |
HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset. |
Immune dysfunction with T-cell inactivation due to calcium entry defect 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Immune dysfunction with T-cell inactivation due to calcium entry defect 1 from the curated CTD Gene-Disease Associations dataset. |
Immune dysfunction with T-cell inactivation due to calcium entry defect 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Immune dysfunction with T-cell inactivation due to calcium entry defect 2 from the curated CTD Gene-Disease Associations dataset. |
thrombocytopenia due to platelet alloimmunization Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease thrombocytopenia due to platelet alloimmunization in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pneumoconiosis due to talc Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pneumoconiosis due to talc in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary spastic paraparesis due to a frame shift mutat Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary spastic paraparesis due to a frame shift mutat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depressed suicide; suicide due to depression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depressed suicide; suicide due to depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
due Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term due in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
anemia due to reduced life span of red cells Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the anemia due to reduced life span of red cells phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
decreased cervical spine flexion due to contractures of posterior cervical muscles Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased cervical spine flexion due to contractures of posterior cervical muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
anemia due to reduced life span of red cells Gene SetFrom HPO Gene-Disease Associations genes associated with the anemia due to reduced life span of red cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
restricted neck movement due to contractures Gene SetFrom HPO Gene-Disease Associations genes associated with the restricted neck movement due to contractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
chronic rhinitis due to narrow nasal airway Gene SetFrom HPO Gene-Disease Associations genes associated with the chronic rhinitis due to narrow nasal airway phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
osteomyelitis due to immunodeficiency Gene SetFrom HPO Gene-Disease Associations genes associated with the osteomyelitis due to immunodeficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
osteomyelitis or necrosis, distal, due to sensory neuropathy (feet) Gene SetFrom HPO Gene-Disease Associations genes associated with the osteomyelitis or necrosis, distal, due to sensory neuropathy (feet) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
bowing of limbs due to multiple fractures Gene SetFrom HPO Gene-Disease Associations genes associated with the bowing of limbs due to multiple fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
respiratory insufficiency due to muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the respiratory insufficiency due to muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
osteomyelitis leading to amputation due to slow healing fractures Gene SetFrom HPO Gene-Disease Associations genes associated with the osteomyelitis leading to amputation due to slow healing fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
weakness due to upper motor neuron dysfunction Gene SetFrom HPO Gene-Disease Associations genes associated with the weakness due to upper motor neuron dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
self-mutilation of tongue and lips due to involuntary movements Gene SetFrom HPO Gene-Disease Associations genes associated with the self-mutilation of tongue and lips due to involuntary movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
respiratory insufficiency due to defective ciliary clearance Gene SetFrom HPO Gene-Disease Associations genes associated with the respiratory insufficiency due to defective ciliary clearance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent infections due to aspiration Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent infections due to aspiration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
generalized hypotonia due to defect at the neuromuscular junction Gene SetFrom HPO Gene-Disease Associations genes associated with the generalized hypotonia due to defect at the neuromuscular junction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
chronic hepatitis due to cryptospridium infection Gene SetFrom HPO Gene-Disease Associations genes associated with the chronic hepatitis due to cryptospridium infection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
subperiosteal erosions due to secondary hyperparathyroidism Gene SetFrom HPO Gene-Disease Associations genes associated with the subperiosteal erosions due to secondary hyperparathyroidism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
painless fractures due to injury Gene SetFrom HPO Gene-Disease Associations genes associated with the painless fractures due to injury phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hepatic abscesses due to immunodeficiency Gene SetFrom HPO Gene-Disease Associations genes associated with the hepatic abscesses due to immunodeficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cellulitis due to immunodeficiency Gene SetFrom HPO Gene-Disease Associations genes associated with the cellulitis due to immunodeficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
decreased sweating due to autonomic dysfunction Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased sweating due to autonomic dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
intermittent episodes of respiratory insufficiency due to muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the intermittent episodes of respiratory insufficiency due to muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
orthostatic hypotension due to autonomic dysfunction Gene SetFrom HPO Gene-Disease Associations genes associated with the orthostatic hypotension due to autonomic dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
{chronic infections, due to mbl deficiency} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {chronic infections, due to mbl deficiency} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{hepatic fibrosis susceptibility due to schistosoma mansoni infection} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {hepatic fibrosis susceptibility due to schistosoma mansoni infection} phenotype from the curated OMIM Gene-Disease Associations dataset. |
thrombophilia due to hrg deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the thrombophilia due to hrg deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
thrombophilia due to thrombomodulin defect Gene SetFrom OMIM Gene-Disease Associations genes associated with the thrombophilia due to thrombomodulin defect phenotype from the curated OMIM Gene-Disease Associations dataset. |
severe combined immunodeficiency due to il2 deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the severe combined immunodeficiency due to il2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
thrombophilia due to protein s deficiency, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the thrombophilia due to protein s deficiency, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
bleeding disorder due to p2rx1 defect Gene SetFrom OMIM Gene-Disease Associations genes associated with the bleeding disorder due to p2rx1 defect phenotype from the curated OMIM Gene-Disease Associations dataset. |
hemolytic anemia due to phosphofructokinase deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the hemolytic anemia due to phosphofructokinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
nephropathy due to cfhr5 deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the nephropathy due to cfhr5 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
encephalopahty, lethal, due to defective mitochondrial peroxisomal fission Gene SetFrom OMIM Gene-Disease Associations genes associated with the encephalopahty, lethal, due to defective mitochondrial peroxisomal fission phenotype from the curated OMIM Gene-Disease Associations dataset. |
megaloblastic anemia due to dihydrofolate reductase deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the megaloblastic anemia due to dihydrofolate reductase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
thrombophilia due to protein s deficiency, autosomal dominant Gene SetFrom OMIM Gene-Disease Associations genes associated with the thrombophilia due to protein s deficiency, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset. |
chronic granulomatous disease, autosomal, due to deficiency of cyba Gene SetFrom OMIM Gene-Disease Associations genes associated with the chronic granulomatous disease, autosomal, due to deficiency of cyba phenotype from the curated OMIM Gene-Disease Associations dataset. |
?isolated growth hormone deficiency due to defect in ghrf Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?isolated growth hormone deficiency due to defect in ghrf phenotype from the curated OMIM Gene-Disease Associations dataset. |
thrombophilia due to heparin cofactor ii deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the thrombophilia due to heparin cofactor ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
obesity, morbid, due to leptin receptor deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the obesity, morbid, due to leptin receptor deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
hypercholesterolemia, due to ligand-defective apo b Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypercholesterolemia, due to ligand-defective apo b phenotype from the curated OMIM Gene-Disease Associations dataset. |
glucocorticoid deficiency, due to acth unresponsiveness Gene SetFrom OMIM Gene-Disease Associations genes associated with the glucocorticoid deficiency, due to acth unresponsiveness phenotype from the curated OMIM Gene-Disease Associations dataset. |
disordered steroidogenesis due to cytochrome p450 oxidoreductase Gene SetFrom OMIM Gene-Disease Associations genes associated with the disordered steroidogenesis due to cytochrome p450 oxidoreductase phenotype from the curated OMIM Gene-Disease Associations dataset. |
hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
muscular dystrophy, congenital, due to partial lama2 deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital, due to partial lama2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
hemorrhagic diathesis due to 'antithrombin' pittsburgh Gene SetFrom OMIM Gene-Disease Associations genes associated with the hemorrhagic diathesis due to 'antithrombin' pittsburgh phenotype from the curated OMIM Gene-Disease Associations dataset. |
immunodeficiency due to purine nucleoside phosphorylase deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the immunodeficiency due to purine nucleoside phosphorylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
hemolytic anemia due to glutathione peroxidase deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the hemolytic anemia due to glutathione peroxidase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset. |
thrombophilia due to protein c deficiency, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the thrombophilia due to protein c deficiency, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
lacticacidemia due to pdx1 deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the lacticacidemia due to pdx1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
ehlers-danlos syndrome, autosomal recessive, due to tenascin x deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the ehlers-danlos syndrome, autosomal recessive, due to tenascin x deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
omphalocele due to duplication of 1p31.3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the omphalocele due to duplication of 1p31.3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
muscular dystrophy, congenital, due to itga7 deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital, due to itga7 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
anemia, hemolytic, due to umph1 deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the anemia, hemolytic, due to umph1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
homocystinuria due to mthfr deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the homocystinuria due to mthfr deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
severe combined immunodeficiency due to ada deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the severe combined immunodeficiency due to ada deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
leigh syndrome due to mitochondrial complex i deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the leigh syndrome due to mitochondrial complex i deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
thrombophilia due to protein c deficiency, autosomal dominant Gene SetFrom OMIM Gene-Disease Associations genes associated with the thrombophilia due to protein c deficiency, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset. |
adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
cirrhosis due to liver phosphorylase kinase deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the cirrhosis due to liver phosphorylase kinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
metachromatic leukodystrophy due to sap-b deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the metachromatic leukodystrophy due to sap-b deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
gigantism due to ghrf hypersecretion Gene SetFrom OMIM Gene-Disease Associations genes associated with the gigantism due to ghrf hypersecretion phenotype from the curated OMIM Gene-Disease Associations dataset. |
obesity, morbid, due to leptin deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the obesity, morbid, due to leptin deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
pseudohyperkalemia, familial, 2, due to red cell leak Gene SetFrom OMIM Gene-Disease Associations genes associated with the pseudohyperkalemia, familial, 2, due to red cell leak phenotype from the curated OMIM Gene-Disease Associations dataset. |
thrombophilia, familial, due to decreased release of plat Gene SetFrom OMIM Gene-Disease Associations genes associated with the thrombophilia, familial, due to decreased release of plat phenotype from the curated OMIM Gene-Disease Associations dataset. |
leigh syndrome, due to cox deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the leigh syndrome, due to cox deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
macrocytic anemia, refractory, due to 5q deletion, somatic Gene SetFrom OMIM Gene-Disease Associations genes associated with the macrocytic anemia, refractory, due to 5q deletion, somatic phenotype from the curated OMIM Gene-Disease Associations dataset. |
growth retardation with deafness and mental retardation due to igf1 deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the growth retardation with deafness and mental retardation due to igf1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyperammonemia due to carbonic anhydrase va deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyperammonemia due to carbonic anhydrase va deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
hemolytic anemia due to g6pd deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the hemolytic anemia due to g6pd deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
{hypercholesterolemia, familial, due to ldlr defect, modifier of} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {hypercholesterolemia, familial, due to ldlr defect, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset. |
hemolytic anemia due to glutathione synthetase deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the hemolytic anemia due to glutathione synthetase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase i/iii deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase i/iii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
{drug-induced liver injury due to flucloxacillin} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {drug-induced liver injury due to flucloxacillin} phenotype from the curated OMIM Gene-Disease Associations dataset. |
thrombophilia due to activated protein c resistance Gene SetFrom OMIM Gene-Disease Associations genes associated with the thrombophilia due to activated protein c resistance phenotype from the curated OMIM Gene-Disease Associations dataset. |
?male pseudohermaphroditism due to defective lh Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?male pseudohermaphroditism due to defective lh phenotype from the curated OMIM Gene-Disease Associations dataset. |
hydrocephalus due to aqueductal stenosis Gene SetFrom OMIM Gene-Disease Associations genes associated with the hydrocephalus due to aqueductal stenosis phenotype from the curated OMIM Gene-Disease Associations dataset. |
bare lymphocyte syndrome, type i, due to tap2 deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the bare lymphocyte syndrome, type i, due to tap2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
thrombophilia due to elevated hrg Gene SetFrom OMIM Gene-Disease Associations genes associated with the thrombophilia due to elevated hrg phenotype from the curated OMIM Gene-Disease Associations dataset. |
hemolytic anemia due to adenylate kinase deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the hemolytic anemia due to adenylate kinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
hemolytic anemia due to glutathione reductase deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the hemolytic anemia due to glutathione reductase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
emphysema due to aat deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the emphysema due to aat deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
obesity, adrenal insufficiency, and red hair due to pomc deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the obesity, adrenal insufficiency, and red hair due to pomc deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
thrombophilia due to antithrombin iii deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the thrombophilia due to antithrombin iii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
erythrocytosis due to bisphosphoglycerate mutase deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the erythrocytosis due to bisphosphoglycerate mutase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyperandrogenism, nonclassic type, due to 21-hydroxylase deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyperandrogenism, nonclassic type, due to 21-hydroxylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
thalassemia due to hb lepore Gene SetFrom OMIM Gene-Disease Associations genes associated with the thalassemia due to hb lepore phenotype from the curated OMIM Gene-Disease Associations dataset. |
rickets due to defect in vitamin d 25-hydroxylation Gene SetFrom OMIM Gene-Disease Associations genes associated with the rickets due to defect in vitamin d 25-hydroxylation phenotype from the curated OMIM Gene-Disease Associations dataset. |
aica-ribosiduria due to atic deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the aica-ribosiduria due to atic deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
hypoaldosteronism, congenital, due to cmo i deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypoaldosteronism, congenital, due to cmo i deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
leigh syndrome due to mitochondrial cox4 deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the leigh syndrome due to mitochondrial cox4 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
methylmalonic aciduria due to transcobalamin receptor defect Gene SetFrom OMIM Gene-Disease Associations genes associated with the methylmalonic aciduria due to transcobalamin receptor defect phenotype from the curated OMIM Gene-Disease Associations dataset. |
chronic granulomatous disease due to deficiency of ncf-2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the chronic granulomatous disease due to deficiency of ncf-2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
chronic granulomatous disease due to deficiency of ncf-1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the chronic granulomatous disease due to deficiency of ncf-1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
thrombophilia, x-linked, due to factor ix defect Gene SetFrom OMIM Gene-Disease Associations genes associated with the thrombophilia, x-linked, due to factor ix defect phenotype from the curated OMIM Gene-Disease Associations dataset. |
hypermethioninemia due to adenosine kinase deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypermethioninemia due to adenosine kinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
{thrombophilia, susceptibility to, due to factor v leiden} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {thrombophilia, susceptibility to, due to factor v leiden} phenotype from the curated OMIM Gene-Disease Associations dataset. |
dystonia, dopa-responsive, due to sepiapterin reductase deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the dystonia, dopa-responsive, due to sepiapterin reductase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
immunodeficiency due to defect in mapbp-interacting protein Gene SetFrom OMIM Gene-Disease Associations genes associated with the immunodeficiency due to defect in mapbp-interacting protein phenotype from the curated OMIM Gene-Disease Associations dataset. |
leigh syndrome due to cytochrome c oxidase deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the leigh syndrome due to cytochrome c oxidase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
pyogenic bacterial infections, recurrent, due to myd88 deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the pyogenic bacterial infections, recurrent, due to myd88 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
neurodegeneration due to cerebral folate transport deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the neurodegeneration due to cerebral folate transport deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
goiter, familial, due to ttf-1 defect Gene SetFrom OMIM Gene-Disease Associations genes associated with the goiter, familial, due to ttf-1 defect phenotype from the curated OMIM Gene-Disease Associations dataset. |
thrombophilia due to thrombin defect Gene SetFrom OMIM Gene-Disease Associations genes associated with the thrombophilia due to thrombin defect phenotype from the curated OMIM Gene-Disease Associations dataset. |
immunodeficiency due to ficolin 3 deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the immunodeficiency due to ficolin 3 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyperfibrinolysis, familial, due to increased release of plat Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyperfibrinolysis, familial, due to increased release of plat phenotype from the curated OMIM Gene-Disease Associations dataset. |
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
leigh syndrome due to mitochondrial complex 1 deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the leigh syndrome due to mitochondrial complex 1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
hemolytic anemia due to triosephosphate isomerase deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the hemolytic anemia due to triosephosphate isomerase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
{resistance to malaria due to g6pd deficiency} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {resistance to malaria due to g6pd deficiency} phenotype from the curated OMIM Gene-Disease Associations dataset. |
hemolytic anemia due to hexokinase deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the hemolytic anemia due to hexokinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
hemosiderosis, systemic, due to aceruloplasminemia Gene SetFrom OMIM Gene-Disease Associations genes associated with the hemosiderosis, systemic, due to aceruloplasminemia phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy due to cpt ii deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy due to cpt ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
emphysema-cirrhosis, due to aat deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the emphysema-cirrhosis, due to aat deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
hypoaldosteronism, congenital, due to cmo ii deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypoaldosteronism, congenital, due to cmo ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
methylmalonic aciduria, vitamin b12-responsive, due to defect in synthesis of adenosylcobalamin, cblb complementation type Gene SetFrom OMIM Gene-Disease Associations genes associated with the methylmalonic aciduria, vitamin b12-responsive, due to defect in synthesis of adenosylcobalamin, cblb complementation type phenotype from the curated OMIM Gene-Disease Associations dataset. |
?male infertility due to acrosin deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?male infertility due to acrosin deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy due to myoadenylate deaminase deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy due to myoadenylate deaminase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
Defective GCLC causes Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency (HAGGSD) Gene Setproteins participating in the Defective GCLC causes Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency (HAGGSD) pathway from the Reactome Pathways dataset. |
Apoptosis-related network due to altered Notch3 in ovarian cancer(Homo sapiens) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the Apoptosis-related network due to altered Notch3 in ovarian cancer(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset. |
Malignant Hyperpyrexia Due To Anesthesia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Hyperpyrexia Due To Anesthesia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pseudohyperkalemia, Familial, 2, Due To Red Cell Leak Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pseudohyperkalemia, Familial, 2, Due To Red Cell Leak in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Functional Diarrhoea (Due To Spastic Colon) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Functional Diarrhoea (Due To Spastic Colon) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Neuropathy Due To And Following Chemotherapy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Neuropathy Due To And Following Chemotherapy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hemolytic Disease Of Fetus Or Newborn Due To Abo Immunization Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hemolytic Disease Of Fetus Or Newborn Due To Abo Immunization in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Viral Gastroenteritis Due To Rotavirus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Viral Gastroenteritis Due To Rotavirus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dementia Due To Alzheimer'S Disease (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dementia Due To Alzheimer'S Disease (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Whooping Cough Due To Unspecified Organism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Whooping Cough Due To Unspecified Organism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Osteopenia Due To Disuse Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Osteopenia Due To Disuse in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Scid Due To Ada Deficiency, Early-Onset Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Scid Due To Ada Deficiency, Early-Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypermethioninemia Due To Adenosine Kinase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypermethioninemia Due To Adenosine Kinase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Disease Due To Parvoviridae Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Disease Due To Parvoviridae in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chronic Respiratory Disease Due To Mycoplasma Gallisepticum Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chronic Respiratory Disease Due To Mycoplasma Gallisepticum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Differentiation Syndrome Due To And Following Chemotherapy Co-Occurrent With Acute Promyelocytic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Differentiation Syndrome Due To And Following Chemotherapy Co-Occurrent With Acute Promyelocytic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Adenocarcinoma Of Lower Third Of Esophagus Due To Barrett Esophagus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Adenocarcinoma Of Lower Third Of Esophagus Due To Barrett Esophagus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Addison'S Disease Due To Autoimmunity Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Addison'S Disease Due To Autoimmunity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adenylate Kinase Deficiency, Hemolytic Anemia Due To Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adenylate Kinase Deficiency, Hemolytic Anemia Due To in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Eye Disorder Due To Diabetes Mellitus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Eye Disorder Due To Diabetes Mellitus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ketoacidosis Due To Acute Alcohol Intoxication Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ketoacidosis Due To Acute Alcohol Intoxication in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Human Anaplasmosis Due To Anaplasma Phagocytophilum Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Human Anaplasmosis Due To Anaplasma Phagocytophilum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypercholesterolemia, Familial, Due To Ligand-Defective Apolipoprotein B Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypercholesterolemia, Familial, Due To Ligand-Defective Apolipoprotein B in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
End Stage Renal Disease Due To Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease End Stage Renal Disease Due To Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Male Infertility With Teratozoospermia Due To Single Gene Mutation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Male Infertility With Teratozoospermia Due To Single Gene Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hydrops Fetalis Due To Alpha Thalassemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hydrops Fetalis Due To Alpha Thalassemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Leigh Syndrome Due To Mitochondrial Complex I Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Leigh Syndrome Due To Mitochondrial Complex I Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Disease Due To Acanthocephala Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Disease Due To Acanthocephala in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fast Acetylator Due To N-Acetyltransferase Enzyme Variant Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fast Acetylator Due To N-Acetyltransferase Enzyme Variant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Anemia, Nonspherocytic Hemolytic, Due To G6Pd Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Anemia, Nonspherocytic Hemolytic, Due To G6Pd Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Antibody Deficiency Due To Defect In Cd19 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Antibody Deficiency Due To Defect In Cd19 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Disease Due To Neisseria Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Disease Due To Neisseria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Osteomyelitis Due To Staphylococcus Aureus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Osteomyelitis Due To Staphylococcus Aureus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chronic Hepatitis Due To Cryptosporidium Infection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chronic Hepatitis Due To Cryptosporidium Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hemosiderosis, Systemic, Due To Aceruloplasminemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hemosiderosis, Systemic, Due To Aceruloplasminemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Infection Due To Brucella Suis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Infection Due To Brucella Suis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Neuronal Ceroid Lipofuscinosis Due To Cathepsin D Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Neuronal Ceroid Lipofuscinosis Due To Cathepsin D Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Intestinal Obstruction Co-Occurrent And Due To Decreased Peristalsis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Intestinal Obstruction Co-Occurrent And Due To Decreased Peristalsis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Inherited Isolated Adrenal Insufficiency Due To Partial Cyp11A1 Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Inherited Isolated Adrenal Insufficiency Due To Partial Cyp11A1 Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Slow Acetylator Due To N-Acetyltransferase Enzyme Variant Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Slow Acetylator Due To N-Acetyltransferase Enzyme Variant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypercholesterolemia Due To Cholesterol 7Alpha-Hydroxylase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypercholesterolemia Due To Cholesterol 7Alpha-Hydroxylase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Body Skin Hyperlaxity Due To Vitamin K Dependent Coagulation Factor Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Body Skin Hyperlaxity Due To Vitamin K Dependent Coagulation Factor Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Infections Due To Aspiration Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Infections Due To Aspiration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Duodenal Obstruction Due To Malrotation Of Intestine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Duodenal Obstruction Due To Malrotation Of Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lipid Storage Myopathy Due To Flavin Adenine Dinucleotide Synthetase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lipid Storage Myopathy Due To Flavin Adenine Dinucleotide Synthetase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Krabbe Disease, Atypical, Due To Saposin A Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Krabbe Disease, Atypical, Due To Saposin A Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Infection Due To Mycobacterium Kansasii Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Infection Due To Mycobacterium Kansasii in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia Due To Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia Due To in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hydronephrosis Due To Pujo Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hydronephrosis Due To Pujo in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thyrotoxicosis Due To Pituitary Thyroid Hormone Resistance Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thyrotoxicosis Due To Pituitary Thyroid Hormone Resistance in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Glutathione Peroxidase Deficiency, Hemolytic Anemia Possibly Due To Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Glutathione Peroxidase Deficiency, Hemolytic Anemia Possibly Due To in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Glutathione Synthetase Deficiency Of Erythrocytes, Hemolytic Anemia Due To Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Glutathione Synthetase Deficiency Of Erythrocytes, Hemolytic Anemia Due To in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hemolytic Anemia Due To Hexokinase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hemolytic Anemia Due To Hexokinase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Disseminated Due To Other Mycobacteria Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Disseminated Due To Other Mycobacteria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Diabetes (Mellitus) Due To Autoimmune Process Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Diabetes (Mellitus) Due To Autoimmune Process in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Diabetes (Mellitus) Due To Immune Mediated Pancreatic Islet Beta-Cell Destruction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Diabetes (Mellitus) Due To Immune Mediated Pancreatic Islet Beta-Cell Destruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Syndromic Multisystem Autoimmune Disease Due To Itch Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Syndromic Multisystem Autoimmune Disease Due To Itch Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Immunodeficiency Syndrome Due To P14 Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Immunodeficiency Syndrome Due To P14 Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Scoliosis Due To Bony Malformation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Scoliosis Due To Bony Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Neonatal Lactic Acidosis Due To Nfs1-Isd11 Complex Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Neonatal Lactic Acidosis Due To Nfs1-Isd11 Complex Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Infection Due To Vancomycin Resistant Staphylococcus Aureus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Infection Due To Vancomycin Resistant Staphylococcus Aureus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Early-Onset Axonal Neuropathy Due To Mitofusin 2 Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Early-Onset Axonal Neuropathy Due To Mitofusin 2 Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acute Renal Failure Due To Ischemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acute Renal Failure Due To Ischemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dementia Due To Parkinson'S Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dementia Due To Parkinson'S Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Urticaria Due To Cold And Heat Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Urticaria Due To Cold And Heat in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Urticaria Due To Cold Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Urticaria Due To Cold in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pseudohermaphroditism, Female, With Hypokalemia, Due To Glucocorticoid Resistance Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pseudohermaphroditism, Female, With Hypokalemia, Due To Glucocorticoid Resistance in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia Due To Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia Due To in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypercoagulability Syndrome Due To Glycosylphosphatidylinositol Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypercoagulability Syndrome Due To Glycosylphosphatidylinositol Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acute Bronchitis Due To Respiratory Syncytial Virus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acute Bronchitis Due To Respiratory Syncytial Virus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Irritant Contact Dermatitis Due To Incontinence Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Irritant Contact Dermatitis Due To Incontinence in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Thrombotic Disease, Due To Protein C Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Thrombotic Disease, Due To Protein C Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Gaucher Disease, Atypical, Due To Saposin C Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Gaucher Disease, Atypical, Due To Saposin C Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Metachromatic Leukodystrophy Due To Saposin B Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Metachromatic Leukodystrophy Due To Saposin B Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hemolytic Disease Of Fetus Or Newborn Due To Rhd Isoimmunization Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hemolytic Disease Of Fetus Or Newborn Due To Rhd Isoimmunization in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Extraoral Halitosis Due To Methanethiol Oxidase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Extraoral Halitosis Due To Methanethiol Oxidase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Complement Component 4, Partial Deficiency Of, Due To Dysfunctional C1 Inhibitor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Complement Component 4, Partial Deficiency Of, Due To Dysfunctional C1 Inhibitor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dermatophilosis Due To Dermatophilus Congolensis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dermatophilosis Due To Dermatophilus Congolensis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Perinatal Jaundice Due To Inspissated Bile Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Perinatal Jaundice Due To Inspissated Bile Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Zinc Deficiency, Neonatal, Due To Low Breast Milk Zinc Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Zinc Deficiency, Neonatal, Due To Low Breast Milk Zinc in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Infection Due To Clostridium Chauvoei Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Infection Due To Clostridium Chauvoei in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Developmental And Speech Delay Due To Sox5 Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Developmental And Speech Delay Due To Sox5 Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chronic Rhinitis Due To Narrow Nasal Airway Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chronic Rhinitis Due To Narrow Nasal Airway in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adult-Onset Distal Myopathy Due To Valosin Containing Protein Mutation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adult-Onset Distal Myopathy Due To Valosin Containing Protein Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Osteomalacia Due To Vitamin D Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Osteomalacia Due To Vitamin D Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Muscle Atrophy Due To Neurologic Disease Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Muscle Atrophy Due To Neurologic Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Respiratory Insufficiency Due To Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Respiratory Insufficiency Due To Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Intermittent Episodes Of Respiratory Insufficiency Due To Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intermittent Episodes Of Respiratory Insufficiency Due To Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Psychomotor Retardation Due To S-Adenosylhomocysteine Hydrolase Deficiency Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Psychomotor Retardation Due To S-Adenosylhomocysteine Hydrolase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Respiratory Insufficiency Due To Defective Ciliary Clearance Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Respiratory Insufficiency Due To Defective Ciliary Clearance in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Orthostatic Hypotension Due To Autonomic Dysfunction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Orthostatic Hypotension Due To Autonomic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Osteomyelitis Leading To Amputation Due To Slow Healing Fractures Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Osteomyelitis Leading To Amputation Due To Slow Healing Fractures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Chromosomal Mosaicism Due To Mitotic Instability Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chromosomal Mosaicism Due To Mitotic Instability in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Weakness Due To Upper Motor Neuron Dysfunction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Weakness Due To Upper Motor Neuron Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cephalhematoma Due To Birth Trauma Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cephalhematoma Due To Birth Trauma in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Generalized Hypotonia Due To Defect At The Neuromuscular Junction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Hypotonia Due To Defect At The Neuromuscular Junction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Bowing Of Limbs Due To Multiple Fractures Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Bowing Of Limbs Due To Multiple Fractures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Restricted Neck Movement Due To Contractures Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Restricted Neck Movement Due To Contractures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Cervical Spine Flexion Due To Contractures Of Posterior Cervical Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Cervical Spine Flexion Due To Contractures Of Posterior Cervical Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Early-Onset Epileptic Encephalopathy And Intellectual Disability Due To Grin2A Mutation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Early-Onset Epileptic Encephalopathy And Intellectual Disability Due To Grin2A Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Painless Fractures Due To Injury Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Painless Fractures Due To Injury in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Sweating Due To Autonomic Dysfunction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Sweating Due To Autonomic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Acanthocytosis Due To Band 3 Ht Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acanthocytosis Due To Band 3 Ht in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Self-Mutilation Of Tongue And Lips Due To Involuntary Movements Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Self-Mutilation Of Tongue And Lips Due To Involuntary Movements in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Apoptosis related network due to altered Notch3 in ovarian cancer Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Apoptosis related network due to altered Notch3 in ovarian cancer pathway from the WikiPathways Pathways 2024 dataset. |
Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects Gene Setproteins participating in the Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects pathway from the Reactome Pathways 2024 dataset. |
Aberrant regulation of mitotic cell cycle due to RB1 defects Gene Setproteins participating in the Aberrant regulation of mitotic cell cycle due to RB1 defects pathway from the Reactome Pathways 2024 dataset. |
Aberrant regulation of mitotic exit in cancer due to RB1 defects Gene Setproteins participating in the Aberrant regulation of mitotic exit in cancer due to RB1 defects pathway from the Reactome Pathways 2024 dataset. |
Defective DNA double strand break response due to BARD1 loss of function Gene Setproteins participating in the Defective DNA double strand break response due to BARD1 loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective DNA double strand break response due to BRCA1 loss of function Gene Setproteins participating in the Defective DNA double strand break response due to BRCA1 loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA1 binding function Gene Setproteins participating in the Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA1 binding function pathway from the Reactome Pathways 2024 dataset. |
Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA2/RAD51/RAD51C binding function Gene Setproteins participating in the Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA2/RAD51/RAD51C binding function pathway from the Reactome Pathways 2024 dataset. |
Defective Inhibition of DNA Recombination at Telomere Due to ATRX Mutations Gene Setproteins participating in the Defective Inhibition of DNA Recombination at Telomere Due to ATRX Mutations pathway from the Reactome Pathways 2024 dataset. |
Defective Inhibition of DNA Recombination at Telomere Due to DAXX Mutations Gene Setproteins participating in the Defective Inhibition of DNA Recombination at Telomere Due to DAXX Mutations pathway from the Reactome Pathways 2024 dataset. |
Defective Intrinsic Pathway for Apoptosis Due to p14ARF Loss of Function Gene Setproteins participating in the Defective Intrinsic Pathway for Apoptosis Due to p14ARF Loss of Function pathway from the Reactome Pathways 2024 dataset. |
Defective homologous recombination repair (HRR) due to BRCA1 loss of function Gene Setproteins participating in the Defective homologous recombination repair (HRR) due to BRCA1 loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective homologous recombination repair (HRR) due to BRCA2 loss of function Gene Setproteins participating in the Defective homologous recombination repair (HRR) due to BRCA2 loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective homologous recombination repair (HRR) due to PALB2 loss of function Gene Setproteins participating in the Defective homologous recombination repair (HRR) due to PALB2 loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective visual phototransduction due to ABCA4 loss of function Gene Setproteins participating in the Defective visual phototransduction due to ABCA4 loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective visual phototransduction due to LRAT loss of function Gene Setproteins participating in the Defective visual phototransduction due to LRAT loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective visual phototransduction due to OPN1LW loss of function Gene Setproteins participating in the Defective visual phototransduction due to OPN1LW loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective visual phototransduction due to OPN1MW loss of function Gene Setproteins participating in the Defective visual phototransduction due to OPN1MW loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective visual phototransduction due to OPN1SW loss of function Gene Setproteins participating in the Defective visual phototransduction due to OPN1SW loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective visual phototransduction due to RDH12 loss of function Gene Setproteins participating in the Defective visual phototransduction due to RDH12 loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective visual phototransduction due to RDH5 loss of function Gene Setproteins participating in the Defective visual phototransduction due to RDH5 loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective visual phototransduction due to STRA6 loss of function Gene Setproteins participating in the Defective visual phototransduction due to STRA6 loss of function pathway from the Reactome Pathways 2024 dataset. |
Evasion of Oncogene Induced Senescence Due to Defective p16INK4A binding to CDK4 Gene Setproteins participating in the Evasion of Oncogene Induced Senescence Due to Defective p16INK4A binding to CDK4 pathway from the Reactome Pathways 2024 dataset. |
Evasion of Oncogene Induced Senescence Due to Defective p16INK4A binding to CDK4 and CDK6 Gene Setproteins participating in the Evasion of Oncogene Induced Senescence Due to Defective p16INK4A binding to CDK4 and CDK6 pathway from the Reactome Pathways 2024 dataset. |
Evasion of Oncogene Induced Senescence Due to p14ARF Defects Gene Setproteins participating in the Evasion of Oncogene Induced Senescence Due to p14ARF Defects pathway from the Reactome Pathways 2024 dataset. |
Evasion of Oncogene Induced Senescence Due to p16INK4A Defects Gene Setproteins participating in the Evasion of Oncogene Induced Senescence Due to p16INK4A Defects pathway from the Reactome Pathways 2024 dataset. |
Loss of function of TP53 in cancer due to loss of tetramerization ability Gene Setproteins participating in the Loss of function of TP53 in cancer due to loss of tetramerization ability pathway from the Reactome Pathways 2024 dataset. |
Severe congenital encephalopathy due to MECP2 mutation Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Severe congenital encephalopathy due to MECP2 mutation from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Male infertility due to globozoospermia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Male infertility due to globozoospermia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Congenital muscular dystrophy due to LMNA mutation Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital muscular dystrophy due to LMNA mutation from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Male infertility due to globozoospermia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Male infertility due to globozoospermia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Male infertility due to acephalic spermatozoa Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Male infertility due to acephalic spermatozoa in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Thrombocytopenia due to platelet alloimmunization Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thrombocytopenia due to platelet alloimmunization in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Polyneuropathy due to drug Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Polyneuropathy due to drug in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital muscular dystrophy due to LMNA mutation Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy due to LMNA mutation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Encephalopathy due to defective mitochondrial and peroxisomal fission 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Encephalopathy due to defective mitochondrial and peroxisomal fission 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Thrombophilia due to activated protein C resistance Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thrombophilia due to activated protein C resistance in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Thrombophilia due to thrombin defect Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thrombophilia due to thrombin defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Multiple epiphyseal dysplasia due to collagen 9 anomaly Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple epiphyseal dysplasia due to collagen 9 anomaly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital muscular dystrophy due to integrin alpha-7 deficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy due to integrin alpha-7 deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Severe congenital encephalopathy due to MECP2 mutation Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Severe congenital encephalopathy due to MECP2 mutation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Thrombophilia due to HRG deficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thrombophilia due to HRG deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
X-linked thrombophilia due to factor IX defect Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked thrombophilia due to factor IX defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive thrombophilia due to protein C deficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive thrombophilia due to protein C deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant thrombophilia due to protein C deficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant thrombophilia due to protein C deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Thrombophilia due to thrombomodulin defect Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thrombophilia due to thrombomodulin defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant thrombophilia due to protein S deficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant thrombophilia due to protein S deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hyperphenylalaninemia due to tetrahydrobiopterin deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hyperphenylalaninemia due to tetrahydrobiopterin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Thrombophilia due to activated protein C resistance Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Thrombophilia due to activated protein C resistance phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Thrombophilia due to protein C deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Thrombophilia due to protein C deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hereditary thrombophilia due to congenital protein C deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary thrombophilia due to congenital protein C deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Methylmalonic aciduria due to complete methylmalonyl-CoA mutase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Methylmalonic aciduria due to complete methylmalonyl-CoA mutase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
SCID due to ADA deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the SCID due to ADA deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Glycogen storage disease due to glycogen branching enzyme deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease due to glycogen branching enzyme deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Predisposition to invasive fungal disease due to CARD9 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Predisposition to invasive fungal disease due to CARD9 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Homocystinuria due to methylene tetrahydrofolate reductase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Homocystinuria due to methylene tetrahydrofolate reductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Thrombophilia due to thrombin defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Thrombophilia due to thrombin defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal recessive ataxia due to ubiquinone deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive ataxia due to ubiquinone deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Glycogen storage disease due to acid maltase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease due to acid maltase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hepatoencephalopathy due to combined oxidative phosphorylation defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hepatoencephalopathy due to combined oxidative phosphorylation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Syndromic multisystem autoimmune disease due to ITCH deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Syndromic multisystem autoimmune disease due to ITCH deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Rubinstein-Taybi syndrome due to EP300 haploinsufficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe combined immunodeficiency due to DCLRE1C deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe combined immunodeficiency due to DCLRE1C deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Immunodeficiency due to ficolin3 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Immunodeficiency due to ficolin3 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Fatal mitochondrial disease due to combined oxidative phosphorylation defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Fatal mitochondrial disease due to combined oxidative phosphorylation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Sulfite oxidase deficiency due to molybdenum cofactor deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Sulfite oxidase deficiency due to molybdenum cofactor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Neonatal intrahepatic cholestasis due to citrin deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal intrahepatic cholestasis due to citrin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Familial hyperthyroidism due to mutations in TSH receptor Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial hyperthyroidism due to mutations in TSH receptor phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hypothyroidism due to TSH receptor mutations Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hypothyroidism due to TSH receptor mutations phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Lissencephaly due to TUBA1A mutation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Lissencephaly due to TUBA1A mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Peroxisome biogenesis disorder due to PEX1 defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Peroxisome biogenesis disorder due to PEX1 defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Alagille syndrome due to a JAG1 point mutation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Alagille syndrome due to a JAG1 point mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Short stature due to growth hormone secretagogue receptor deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Short stature due to growth hormone secretagogue receptor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Interstitial lung disease due to ABCA3 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Interstitial lung disease due to ABCA3 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Lissencephaly due to LIS1 mutation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Lissencephaly due to LIS1 mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Obesity due to leptin receptor gene deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Obesity due to leptin receptor gene deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Ehlers-Danlos syndrome due to tenascin-X deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Ehlers-Danlos syndrome due to tenascin-X deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Short stature due to partial GHR deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Short stature due to partial GHR deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital lipoid adrenal hyperplasia due to STAR deficency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital lipoid adrenal hyperplasia due to STAR deficency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
T-B+ severe combined immunodeficiency due to JAK3 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the T-B+ severe combined immunodeficiency due to JAK3 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Rubinstein-Taybi syndrome due to CREBBP mutations Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Rubinstein-Taybi syndrome due to CREBBP mutations phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Glycogen storage disease due to phosphoglycerate kinase 1 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease due to phosphoglycerate kinase 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hydrocephalus due to aqueductal stenosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hydrocephalus due to aqueductal stenosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
X-linked lymphoproliferative disease due to SH2D1A deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked lymphoproliferative disease due to SH2D1A deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
X-linked Mendelian susceptibility to mycobacterial diseases due to CYBB deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked Mendelian susceptibility to mycobacterial diseases due to CYBB deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Lissencephaly due to doublecortin gene mutation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Lissencephaly due to doublecortin gene mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Glycogen storage disease due to glucose-6-phosphatase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease due to glucose-6-phosphatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Combined immunodeficiency due to CD3gamma deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Combined immunodeficiency due to CD3gamma deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Leigh syndrome due to mitochondrial complex IV deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Leigh syndrome due to mitochondrial complex IV deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Dopa-responsive dystonia due to sepiapterin reductase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Dopa-responsive dystonia due to sepiapterin reductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Combined immunodeficiency due to partial RAG1 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Combined immunodeficiency due to partial RAG1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Combined immunodeficiency due to ZAP70 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Combined immunodeficiency due to ZAP70 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Thrombophilia due to protein S deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Thrombophilia due to protein S deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Obesity due to pro-opiomelanocortin deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Obesity due to pro-opiomelanocortin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Gaucher disease due to saposin C deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Gaucher disease due to saposin C deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Krabbe disease due to saposin A deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Krabbe disease due to saposin A deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hemolytic anemia due to glucophosphate isomerase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hemolytic anemia due to glucophosphate isomerase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Overgrowth syndrome and/or cerebral malformations due to abnormalities in MTOR pathway genes Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Overgrowth syndrome and/or cerebral malformations due to abnormalities in MTOR pathway genes phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital muscular dystrophy due to partial LAMA2 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital muscular dystrophy due to partial LAMA2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Obesity due to melanocortin 4 receptor deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Obesity due to melanocortin 4 receptor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital muscular dystrophy due to LMNA mutation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital muscular dystrophy due to LMNA mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Growth delay due to insulin-like growth factor I resistance Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Growth delay due to insulin-like growth factor I resistance phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hyperinsulinism due to HNF1A deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hyperinsulinism due to HNF1A deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Short stature due to growth hormone qualitative anomaly Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Short stature due to growth hormone qualitative anomaly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Glycogen storage disorder due to hepatic glycogen synthase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disorder due to hepatic glycogen synthase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Encephalopathy due to GLUT1 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Encephalopathy due to GLUT1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hyperinsulinism due to glucokinase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hyperinsulinism due to glucokinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Glycogen storage disease due to muscle beta-enolase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease due to muscle beta-enolase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Retinal ciliopathy due to mutation in the retinitis pigmentosa-1 gene Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal ciliopathy due to mutation in the retinitis pigmentosa-1 gene phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Combined immunodeficiency due to LRBA deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Combined immunodeficiency due to LRBA deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Atypical severe combined immunodeficiency due to complete RAG1/2 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Atypical severe combined immunodeficiency due to complete RAG1/2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Combined immunodeficiency due to STK4 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Combined immunodeficiency due to STK4 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Combined immunodeficiency due to STIM1 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Combined immunodeficiency due to STIM1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Epidermolysis bullosa simplex due to plakophilin deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Epidermolysis bullosa simplex due to plakophilin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe combined immunodeficiency due to CARD11 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe combined immunodeficiency due to CARD11 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Glycogen storage disease due to SLC37A4 mutation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease due to SLC37A4 mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Combined immunodeficiency due to DOCK8 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Combined immunodeficiency due to DOCK8 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital muscular dystrophy due to integrin alpha-7 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital muscular dystrophy due to integrin alpha-7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Limb-girdle muscular dystrophy due to POMK deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Limb-girdle muscular dystrophy due to POMK deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe early-onset pulmonary alveolar proteinosis due to MARS deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe early-onset pulmonary alveolar proteinosis due to MARS deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Vasculitis due to ADA2 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Vasculitis due to ADA2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Glycogen storage disease due to muscle and heart glycogen synthase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease due to muscle and heart glycogen synthase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Microcephalic primordial dwarfism due to RTTN deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Microcephalic primordial dwarfism due to RTTN deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Ketoacidosis due to monocarboxylate transporter-1 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Ketoacidosis due to monocarboxylate transporter-1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Metabolic myopathy due to lactate transporter defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Metabolic myopathy due to lactate transporter defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Microcephalic primordial dwarfism due to ZNF335 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Microcephalic primordial dwarfism due to ZNF335 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autism spectrum disorder due to AUTS2 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autism spectrum disorder due to AUTS2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Pyogenic bacterial infections due to MyD88 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Pyogenic bacterial infections due to MyD88 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Alagille syndrome due to a NOTCH2 point mutation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Alagille syndrome due to a NOTCH2 point mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Methylmalonic acidemia due to transcobalamin receptor defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Methylmalonic acidemia due to transcobalamin receptor defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood encephalopathy due to thiamine pyrophosphokinase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood encephalopathy due to thiamine pyrophosphokinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe combined immunodeficiency due to CTPS1 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe combined immunodeficiency due to CTPS1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal recessive severe congenital neutropenia due to CSF3R deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive severe congenital neutropenia due to CSF3R deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Neurofibromatosis due to NF1 mutation or intragenic deletion Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Neurofibromatosis due to NF1 mutation or intragenic deletion phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |