Familial glucocorticoid deficiency

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Results for "Familial glucocorticoid deficiency": 1004 gene sets

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familial glucocorticoid deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease familial glucocorticoid deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Familial Glucocorticoid Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Glucocorticoid Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial glucocorticoid deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Familial glucocorticoid deficiency from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Familial glucocorticoid deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial glucocorticoid deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial Glucocorticoid Deficiency 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Glucocorticoid Deficiency 1 from the curated CTD Gene-Disease Associations dataset.
Glucocorticoid deficiency 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glucocorticoid deficiency 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glucocorticoid deficiency 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glucocorticoid deficiency 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glucocorticoid deficiency with achalasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glucocorticoid deficiency with achalasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glucocorticoid Deficiency 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glucocorticoid Deficiency 2 from the curated CTD Gene-Disease Associations dataset.
Glucocorticoid Deficiency 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glucocorticoid Deficiency 3 from the curated CTD Gene-Disease Associations dataset.
NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT from the curated CTD Gene-Disease Associations dataset.
glucocorticoid deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease glucocorticoid deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glucocorticoid deficiency, due to acth unresponsiveness Gene Set From OMIM Gene-Disease Associations genes associated with the glucocorticoid deficiency, due to acth unresponsiveness phenotype from the curated OMIM Gene-Disease Associations dataset.
natural killer cell and glucocorticoid deficiency with dna repair defect Gene Set From OMIM Gene-Disease Associations genes associated with the natural killer cell and glucocorticoid deficiency with dna repair defect phenotype from the curated OMIM Gene-Disease Associations dataset.
glucocorticoid deficiency 2 Gene Set From OMIM Gene-Disease Associations genes associated with the glucocorticoid deficiency 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
glucocorticoid deficiency 3 Gene Set From OMIM Gene-Disease Associations genes associated with the glucocorticoid deficiency 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
glucocorticoid deficiency 4 Gene Set From OMIM Gene-Disease Associations genes associated with the glucocorticoid deficiency 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
Glucocorticoid Deficiency With Achalasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Glucocorticoid Deficiency With Achalasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Glucocorticoid Receptor Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Glucocorticoid Receptor Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Glucocorticoid Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Glucocorticoid Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Glucocorticoid deficiency 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Glucocorticoid deficiency 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN from the curated CTD Gene-Disease Associations dataset.
amyloidosis, familial; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis, familial; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
albuminuria; amyloidosis, familial; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease albuminuria; amyloidosis, familial; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple familial trichoepithelioma and familial cylindromatosis Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple familial trichoepithelioma and familial cylindromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis, familial; familial mediterranean fever; Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis, familial; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hemiplegic migraine and benign familial infantile convulsions Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hemiplegic migraine and benign familial infantile convulsions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Pseudohermaphroditism, female, with hypokalemia, due to glucocorticoid resistance Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pseudohermaphroditism, female, with hypokalemia, due to glucocorticoid resistance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glucocorticoid resistance, generalized Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glucocorticoid resistance, generalized phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glucocorticoid-Remediable Aldosteronism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glucocorticoid-Remediable Aldosteronism from the curated CTD Gene-Disease Associations dataset.
glucocorticoid-remediable aldosteronism Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease glucocorticoid-remediable aldosteronism in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bcli restriction fragment length polymorphism at the glucocorticoid receptor gene locus Gene Set From GAD Gene-Disease Associations genes associated with the disease bcli restriction fragment length polymorphism at the glucocorticoid receptor gene locus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glucocorticoid sensitivity Gene Set From GAD Gene-Disease Associations genes associated with the disease glucocorticoid sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glucocorticoid Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term glucocorticoid in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
positive regulation of glucocorticoid biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of glucocorticoid biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of glucocorticoid receptor signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of glucocorticoid receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
cellular response to glucocorticoid stimulus Gene Set From GO Biological Process Annotations 2015 genes participating in the cellular response to glucocorticoid stimulus biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of glucocorticoid mediated signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of glucocorticoid mediated signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of glucocorticoid secretion Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of glucocorticoid secretion biological process from the curated GO Biological Process Annotations 2015 dataset.
glucocorticoid receptor signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the glucocorticoid receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
response to glucocorticoid Gene Set From GO Biological Process Annotations 2015 genes participating in the response to glucocorticoid biological process from the curated GO Biological Process Annotations 2015 dataset.
glucocorticoid mediated signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the glucocorticoid mediated signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of glucocorticoid metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of glucocorticoid metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
glucocorticoid biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the glucocorticoid biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
glucocorticoid metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the glucocorticoid metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of glucocorticoid metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of glucocorticoid metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of glucocorticoid metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of glucocorticoid metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
glucocorticoid secretion Gene Set From GO Biological Process Annotations 2015 genes participating in the glucocorticoid secretion biological process from the curated GO Biological Process Annotations 2015 dataset.
glucocorticoid catabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the glucocorticoid catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of glucocorticoid secretion Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of glucocorticoid secretion biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of glucocorticoid receptor signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of glucocorticoid receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of glucocorticoid biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of glucocorticoid biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of glucocorticoid secretion Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of glucocorticoid secretion biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of glucocorticoid mediated signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of glucocorticoid mediated signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of glucocorticoid receptor signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of glucocorticoid receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of glucocorticoid biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of glucocorticoid biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
glucocorticoid receptor activity Gene Set From GO Molecular Function Annotations 2015 genes performing the glucocorticoid receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
glucocorticoid-activated rna polymerase ii transcription factor binding transcription factor activity Gene Set From GO Molecular Function Annotations 2015 genes performing the glucocorticoid-activated rna polymerase ii transcription factor binding transcription factor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
glucocorticoid receptor binding Gene Set From GO Molecular Function Annotations 2015 genes performing the glucocorticoid receptor binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
abnormality of circulating glucocorticoid level Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating glucocorticoid level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of circulating glucocorticoid level Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of circulating glucocorticoid level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Glucocorticoid receptor Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Glucocorticoid receptor protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Glucocorticoid-induced transcript 1 protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Glucocorticoid-induced transcript 1 protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Glucocorticoid-induced transcript 1/FAM117 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Glucocorticoid-induced transcript 1/FAM117 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Glucocorticoid modulatory element-binding protein 1/2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Glucocorticoid modulatory element-binding protein 1/2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
decreased circulating glucocorticoid level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating glucocorticoid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased circulating glucocorticoid level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased circulating glucocorticoid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal circulating glucocorticoid level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating glucocorticoid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
glucocorticoid resistance Gene Set From OMIM Gene-Disease Associations genes associated with the glucocorticoid resistance phenotype from the curated OMIM Gene-Disease Associations dataset.
aldosteronism, glucocorticoid-remediable Gene Set From OMIM Gene-Disease Associations genes associated with the aldosteronism, glucocorticoid-remediable phenotype from the curated OMIM Gene-Disease Associations dataset.
{glucocorticoid therapy, response to} Gene Set From OMIM Gene-Disease Associations genes associated with the {glucocorticoid therapy, response to} phenotype from the curated OMIM Gene-Disease Associations dataset.
glucocorticoid Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term glucocorticoid in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
Rapid glucocorticoid signaling Gene Set From PID Pathways proteins participating in the Rapid glucocorticoid signaling pathway from the PID Pathways dataset.
Glucocorticoid receptor regulatory network Gene Set From PID Pathways proteins participating in the Glucocorticoid receptor regulatory network pathway from the PID Pathways dataset.
Glucocorticoid biosynthesis Gene Set From Reactome Pathways 2014 proteins participating in the Glucocorticoid biosynthesis pathway from the Reactome Pathways dataset.
Glucocorticoid & Mineralcorticoid Metabolism(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Glucocorticoid & Mineralcorticoid Metabolism(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Glucocorticoid & Mineralcorticoid Metabolism(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Glucocorticoid & Mineralcorticoid Metabolism(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Glucocorticoid-Remediable Aldosteronism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Glucocorticoid-Remediable Aldosteronism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Glucocorticoid Resistance Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Glucocorticoid Resistance in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pseudohermaphroditism, Female, With Hypokalemia, Due To Glucocorticoid Resistance Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pseudohermaphroditism, Female, With Hypokalemia, Due To Glucocorticoid Resistance in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Glucocorticoid Resistance, Cellular Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Glucocorticoid Resistance, Cellular in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
negative regulation of glucocorticoid receptor signaling pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of glucocorticoid receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
glucocorticoid receptor signaling pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the glucocorticoid receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
cellular response to glucocorticoid stimulus Gene Set From GO Biological Process Annotations 2023 genes participating in the cellular response to glucocorticoid stimulus biological process from the curated GO Biological Process Annotations 2023 dataset.
response to glucocorticoid Gene Set From GO Biological Process Annotations 2023 genes participating in the response to glucocorticoid biological process from the curated GO Biological Process Annotations 2023 dataset.
glucocorticoid biosynthetic process Gene Set From GO Biological Process Annotations 2023 genes participating in the glucocorticoid biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset.
glucocorticoid metabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the glucocorticoid metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
glucocorticoid catabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the glucocorticoid catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of glucocorticoid receptor signaling pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of glucocorticoid receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of glucocorticoid metabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of glucocorticoid metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of glucocorticoid receptor signaling pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of glucocorticoid receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of glucocorticoid biosynthetic process Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of glucocorticoid biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of glucocorticoid secretion Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of glucocorticoid secretion biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of glucocorticoid biosynthetic process Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of glucocorticoid biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of glucocorticoid secretion Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of glucocorticoid secretion biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of glucocorticoid biosynthetic process Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of glucocorticoid biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset.
glucocorticoid secretion Gene Set From GO Biological Process Annotations 2023 genes participating in the glucocorticoid secretion biological process from the curated GO Biological Process Annotations 2023 dataset.
nuclear glucocorticoid receptor binding Gene Set From GO Molecular Function Annotations 2023 genes performing the nuclear glucocorticoid receptor binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
decreased circulating glucocorticoid level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating glucocorticoid level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Glucocorticoid receptor pathway Gene Set From WikiPathways Pathways 2024 proteins participating in the Glucocorticoid receptor pathway pathway from the WikiPathways Pathways 2024 dataset.
Classical pathway of steroidogenesis with glucocorticoid and mineralocorticoid metabolism Gene Set From WikiPathways Pathways 2024 proteins participating in the Classical pathway of steroidogenesis with glucocorticoid and mineralocorticoid metabolism pathway from the WikiPathways Pathways 2024 dataset.
Glucocorticoid biosynthesis Gene Set From WikiPathways Pathways 2024 proteins participating in the Glucocorticoid biosynthesis pathway from the WikiPathways Pathways 2024 dataset.
Glucocorticoid biosynthesis Gene Set From Reactome Pathways 2024 proteins participating in the Glucocorticoid biosynthesis pathway from the Reactome Pathways 2024 dataset.
negative regulation of nuclear receptor-mediated glucocorticoid signaling pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of nuclear receptor-mediated glucocorticoid signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of glucocorticoid biosynthetic process Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of glucocorticoid biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.
cellular response to glucocorticoid stimulus Gene Set From GO Biological Process Annotations 2025 genes participating in the cellular response to glucocorticoid stimulus biological process from the curated GO Biological Process Annotations 2025 dataset.
response to glucocorticoid Gene Set From GO Biological Process Annotations 2025 genes participating in the response to glucocorticoid biological process from the curated GO Biological Process Annotations 2025 dataset.
glucocorticoid biosynthetic process Gene Set From GO Biological Process Annotations 2025 genes participating in the glucocorticoid biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.
glucocorticoid metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the glucocorticoid metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
nuclear receptor-mediated glucocorticoid signaling pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the nuclear receptor-mediated glucocorticoid signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
glucocorticoid catabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the glucocorticoid catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of nuclear receptor-mediated glucocorticoid signaling pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of nuclear receptor-mediated glucocorticoid signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of glucocorticoid metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of glucocorticoid metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of nuclear receptor-mediated glucocorticoid signaling pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of nuclear receptor-mediated glucocorticoid signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of glucocorticoid metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of glucocorticoid metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of glucocorticoid biosynthetic process Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of glucocorticoid biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of glucocorticoid secretion Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of glucocorticoid secretion biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of glucocorticoid biosynthetic process Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of glucocorticoid biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of glucocorticoid secretion Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of glucocorticoid secretion biological process from the curated GO Biological Process Annotations 2025 dataset.
glucocorticoid secretion Gene Set From GO Biological Process Annotations 2025 genes participating in the glucocorticoid secretion biological process from the curated GO Biological Process Annotations 2025 dataset.
nuclear glucocorticoid receptor binding Gene Set From GO Molecular Function Annotations 2025 genes performing the nuclear glucocorticoid receptor binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
glucocorticoid-remediable aldosteronism Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease glucocorticoid-remediable aldosteronism in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
glucocorticoid-induced osteoporosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease glucocorticoid-induced osteoporosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cd8 deficiency, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cd8 deficiency, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
CD8 Deficiency, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CD8 Deficiency, Familial from the curated CTD Gene-Disease Associations dataset.
Familial HDL deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial HDL deficiency from the curated CTD Gene-Disease Associations dataset.
Familial apoceruloplasmin deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial apoceruloplasmin deficiency from the curated CTD Gene-Disease Associations dataset.
familial lipoprotein lipase deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial lipoprotein lipase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial lipoprotein lipase deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial lipoprotein lipase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cryopyrin-associated periodic syndromes; familial mediterranean fever; mevalonate kinase deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease cryopyrin-associated periodic syndromes; familial mediterranean fever; mevalonate kinase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
[igg receptor i, phagocytic, familial deficiency of] Gene Set From OMIM Gene-Disease Associations genes associated with the [igg receptor i, phagocytic, familial deficiency of] phenotype from the curated OMIM Gene-Disease Associations dataset.
cd8 deficiency, familial Gene Set From OMIM Gene-Disease Associations genes associated with the cd8 deficiency, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
Familial Hdl Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hdl Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Lcat Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Lcat Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Lipoprotein Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Lipoprotein Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Apolipoprotein C-Ii Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Apolipoprotein C-Ii Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cd8 Deficiency, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cd8 Deficiency, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Multiple Factor Deficiency Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Factor Deficiency Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Apoceruloplasmin Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Apoceruloplasmin Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Multiple Coagulation Factor Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Coagulation Factor Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Natural Killer Cell Deficiency, Familial Isolated Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Natural Killer Cell Deficiency, Familial Isolated in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Igg Receptor I, Phagocytic, Familial Deficiency Of Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Igg Receptor I, Phagocytic, Familial Deficiency Of in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Familial isolated deficiency of vitamin E Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Familial isolated deficiency of vitamin E from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Familial lipoprotein lipase deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Familial lipoprotein lipase deficiency from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Familial lipoprotein lipase deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial lipoprotein lipase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial isolated deficiency of vitamin E Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial isolated deficiency of vitamin E in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial apolipoprotein C-II deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial apolipoprotein C-II deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial GPIHBP1 deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial GPIHBP1 deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial lipase maturation factor 1 deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial lipase maturation factor 1 deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neuraminidase deficiency with beta-galactosidase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuraminidase deficiency with beta-galactosidase deficiency from the curated CTD Gene-Disease Associations dataset.
MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE from the curated CTD Gene-Disease Associations dataset.
eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; iron deficiency anaemia; tuberculosis, pulmonary Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
folic acid deficiency; fractures, bone; osteoporosis, postmenopausal; riboflavin deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease folic acid deficiency; fractures, bone; osteoporosis, postmenopausal; riboflavin deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia; iron overload Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choline deficiency; dna damage; folic acid deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease choline deficiency; dna damage; folic acid deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
folic acid deficiency; pregnancy complications; prenatal exposure delayed effects; psychomotor disorders; vitamin b 12 deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease folic acid deficiency; pregnancy complications; prenatal exposure delayed effects; psychomotor disorders; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; beta thalassemia; beta-thalassemia; iron deficiency anaemia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; beta thalassemia; beta-thalassemia; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; iron deficiency anaemia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
protein c deficiency; protein s deficiency; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease protein c deficiency; protein s deficiency; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
folic acid deficiency; hyperhomocysteinemia; thromboembolism; venous insufficiency; vitamin b 12 deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease folic acid deficiency; hyperhomocysteinemia; thromboembolism; venous insufficiency; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; iron deficiency anaemia; iron overload Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neoplasms; protein c deficiency; protein s deficiency; venous thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease neoplasms; protein c deficiency; protein s deficiency; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; folic acid deficiency; hyperhomocysteinemia; kidney failure, chronic; vitamin b 12 deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; folic acid deficiency; hyperhomocysteinemia; kidney failure, chronic; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Defective GSS causes Glutathione synthetase deficiency (GSS deficiency) Gene Set From Reactome Pathways 2014 proteins participating in the Defective GSS causes Glutathione synthetase deficiency (GSS deficiency) pathway from the Reactome Pathways dataset.
Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency) Gene Set From Reactome Pathways 2014 proteins participating in the Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency) pathway from the Reactome Pathways dataset.
Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency) Gene Set From Reactome Pathways 2014 proteins participating in the Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency) pathway from the Reactome Pathways dataset.
Defective HK1 causes hexokinase deficiency (HK deficiency) Gene Set From Reactome Pathways 2024 proteins participating in the Defective HK1 causes hexokinase deficiency (HK deficiency) pathway from the Reactome Pathways 2024 dataset.
Familial Mediterranean fever Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial Mediterranean fever phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thrombocytosis, benign familial microcytic Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thrombocytosis, benign familial microcytic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign familial neonatal-infantile seizures Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal-infantile seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neurofibromatosis, familial spinal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neurofibromatosis, familial spinal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tumoral calcinosis, familial, hyperphosphatemic Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tumoral calcinosis, familial, hyperphosphatemic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Febrile seizures, familial, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Febrile seizures, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial restrictive cardiomyopathy 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial restrictive cardiomyopathy 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gaze palsy, familial horizontal, with progressive scoliosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gaze palsy, familial horizontal, with progressive scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hemiplegic migraine type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hemiplegic migraine type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hemiplegic migraine type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hemiplegic migraine type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hemiplegic migraine type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hemiplegic migraine type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Erythrocytosis, familial, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Erythrocytosis, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Erythrocytosis, familial, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Erythrocytosis, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Erythrocytosis, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Erythrocytosis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic aneurysm, familial thoracic 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial X-linked hypophosphatemic vitamin D refractory rickets Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial X-linked hypophosphatemic vitamin D refractory rickets phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile convulsions and paroxysmal choreoathetosis, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile convulsions and paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign familial neonatal seizures 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal seizures 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign familial neonatal seizures 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal seizures 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperuricemic nephropathy, familial juvenile, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperuricemic nephropathy, familial juvenile, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial cancer of breast Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial cancer of breast phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial benign pemphigus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial benign pemphigus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Episodic pain syndrome, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Episodic pain syndrome, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperpigmentation, familial progressive, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperpigmentation, familial progressive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial aortopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial aortopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Digital arthropathy-brachydactyly, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Digital arthropathy-brachydactyly, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Episodic pain syndrome, familial, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Episodic pain syndrome, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular dysplasia, familial, 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Febrile seizures, familial, 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Febrile seizures, familial, 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial benign hypercalcemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial benign hypercalcemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial visceral amyloidosis, Ostertag type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial visceral amyloidosis, Ostertag type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dementia familial British Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dementia familial British phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial porencephaly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial porencephaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 17 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 15 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypocalciuric hypercalcemia, familial, type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypocalciuric hypercalcemia, familial, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
familial hyperinsulinism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the familial hyperinsulinism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperinsulinemic hypoglycemia familial 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperinsulinemic hypoglycemia familial 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Febrile seizures, familial, 3b Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Febrile seizures, familial, 3b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Paroxysmal familial ventricular fibrillation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Paroxysmal familial ventricular fibrillation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypercholesterolemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypercholesterolemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hidradenitis suppurativa, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hidradenitis suppurativa, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dementia, familial Danish Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dementia, familial Danish phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial intrahepatic cholestasis 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial intrahepatic cholestasis 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial intrahepatic cholestasis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial intrahepatic cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign familial hematuria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial hematuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial heart block type 1A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial heart block type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial heart block type 1B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial heart block type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial dysautonomia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial dysautonomia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial febrile seizures 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial febrile seizures 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fleck retina, familial benign Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fleck retina, familial benign phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked familial exudative vitreoretinopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked familial exudative vitreoretinopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial colorectal cancer Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial colorectal cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial porphyria cutanea tarda Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial porphyria cutanea tarda phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 20 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 20 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial intrahepatic cholestasis 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial intrahepatic cholestasis 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Advanced sleep phase syndrome, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Advanced sleep phase syndrome, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myoclonus, familial cortical Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myoclonus, familial cortical phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Migraine, familial basilar Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Migraine, familial basilar phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Breast-ovarian cancer, familial 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Breast-ovarian cancer, familial 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypercholanemia, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypercholanemia, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bone marrow failure, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bone marrow failure, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic aneurysm, familial thoracic 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Advanced sleep phase syndrome, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Advanced sleep phase syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Candidiasis, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Candidiasis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Candidiasis, familial, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Candidiasis, familial, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypokalemia-hypomagnesemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypokalemia-hypomagnesemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenia, limb-girdle, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenia, limb-girdle, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 17 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 16 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 15 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hemophagocytic lymphohistiocytosis, familial, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hemophagocytic lymphohistiocytosis, familial, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hemophagocytic lymphohistiocytosis, familial, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hemophagocytic lymphohistiocytosis, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hemophagocytic lymphohistiocytosis, familial, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hemophagocytic lymphohistiocytosis, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hemophagocytic lymphohistiocytosis, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hemophagocytic lymphohistiocytosis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ventricular fibrillation, paroxysmal familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ventricular fibrillation, paroxysmal familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial platelet disorder with associated myeloid malignancy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial platelet disorder with associated myeloid malignancy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial erythrocytosis, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial erythrocytosis, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial medullary thyroid carcinoma Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial medullary thyroid carcinoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperinsulinemic hypoglycemia, familial, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperinsulinemic hypoglycemia, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic aneurysm, familial thoracic 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic aneurysm, familial thoracic 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic aneurysm, familial thoracic 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperlipidemia, familial combined Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperlipidemia, familial combined phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial amyloid polyneuropathy, Iowa type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial amyloid polyneuropathy, Iowa type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial encephalopathy with neuroserpin inclusion bodies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial encephalopathy with neuroserpin inclusion bodies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, familial adult myoclonic, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, familial adult myoclonic, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial myxoma, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial myxoma, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lipodystrophy, familial partial, type 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lipodystrophy, familial partial, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lipodystrophy, familial partial, type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lipodystrophy, familial partial, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypocalciuric hypercalcemia, familial, type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypocalciuric hypercalcemia, familial, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypocalciuric hypercalcemia, familial, type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypocalciuric hypercalcemia, familial, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial multiple polyposis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial multiple polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial juvenile gout Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial juvenile gout phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardiomyopathy:Familial hypertrophic cardiomyopathy 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy:Familial hypertrophic cardiomyopathy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypobetalipoproteinemia, familial, associated with apob32 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypobetalipoproteinemia, familial, associated with apob32 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Breast-ovarian cancer, familial 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Breast-ovarian cancer, familial 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary cancer-predisposing syndrome:Erythrocytosis, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Erythrocytosis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Primary familial hypertrophic cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Primary familial hypertrophic cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial type 3 hyperlipoproteinemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial type 3 hyperlipoproteinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tumoral calcinosis, familial, normophosphatemic Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tumoral calcinosis, familial, normophosphatemic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial infantile myasthenia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial infantile myasthenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked familial atypical mycobacteriosis, type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked familial atypical mycobacteriosis, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperthyroxinemia, familial dysalbuminemic Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperthyroxinemia, familial dysalbuminemic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial type 5 hyperlipoproteinemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial type 5 hyperlipoproteinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cutaneous telangiectasia and cancer syndrome, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cutaneous telangiectasia and cancer syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial renal glucosuria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial renal glucosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial pulmonary capillary hemangiomatosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial pulmonary capillary hemangiomatosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypoalphalipoproteinemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypoalphalipoproteinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial renal hypouricemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial renal hypouricemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
HYPERALDOSTERONISM, FAMILIAL, TYPE III Gene Set From ClinVar Gene-Phenotype Associations genes associated with the HYPERALDOSTERONISM, FAMILIAL, TYPE III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myoclonic epilepsy, familial infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myoclonic epilepsy, familial infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypoplastic, glomerulocystic kidney Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypoplastic, glomerulocystic kidney phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial cold urticaria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial cold urticaria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic Aneurysm, Familial Abdominal 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Abdominal 2 from the curated CTD Gene-Disease Associations dataset.
Familial myelofibrosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial myelofibrosis from the curated CTD Gene-Disease Associations dataset.
Nephronophthisis, familial juvenile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nephronophthisis, familial juvenile from the curated CTD Gene-Disease Associations dataset.
Eosinophilia, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Eosinophilia, Familial from the curated CTD Gene-Disease Associations dataset.
Hyperlipidemia, Familial Combined Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperlipidemia, Familial Combined from the curated CTD Gene-Disease Associations dataset.
Platelet Disorder, Familial, with Associated Myeloid Malignancy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Platelet Disorder, Familial, with Associated Myeloid Malignancy from the curated CTD Gene-Disease Associations dataset.
Hyperinsulinemic hypoglycemia, familial, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperinsulinemic hypoglycemia, familial, 6 from the curated CTD Gene-Disease Associations dataset.
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.
Pemphigus, Benign Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pemphigus, Benign Familial from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Restrictive, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 1 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 9 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 8 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 2 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 6 from the curated CTD Gene-Disease Associations dataset.
Amyloidosis, familial visceral Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Amyloidosis, familial visceral from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Hypertrophic, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Hypertrophic, Familial from the curated CTD Gene-Disease Associations dataset.
Gaze Palsy, Familial Horizontal, with Progressive Scoliosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gaze Palsy, Familial Horizontal, with Progressive Scoliosis from the curated CTD Gene-Disease Associations dataset.
Atrial Fibrillation, Familial, 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 8 from the curated CTD Gene-Disease Associations dataset.
Atrial Fibrillation, Familial, 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 7 from the curated CTD Gene-Disease Associations dataset.
Atrial Fibrillation, Familial, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 6 from the curated CTD Gene-Disease Associations dataset.
Atrial Fibrillation, Familial, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 4 from the curated CTD Gene-Disease Associations dataset.
Cholestasis, progressive familial intrahepatic 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 1 from the curated CTD Gene-Disease Associations dataset.
Cholestasis, progressive familial intrahepatic 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 2 from the curated CTD Gene-Disease Associations dataset.
Myasthenia, Familial Infantile, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myasthenia, Familial Infantile, 1 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 4 from the curated CTD Gene-Disease Associations dataset.
Aortic Aneurysm, Familial Abdominal 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Abdominal 1 from the curated CTD Gene-Disease Associations dataset.
STUTTERING, FAMILIAL PERSISTENT, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease STUTTERING, FAMILIAL PERSISTENT, 1 from the curated CTD Gene-Disease Associations dataset.
Dementia, familial British Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dementia, familial British from the curated CTD Gene-Disease Associations dataset.
Candidiasis familial chronic mucocutaneous, autosomal recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Candidiasis familial chronic mucocutaneous, autosomal recessive from the curated CTD Gene-Disease Associations dataset.
Gliosis, Familial Progressive Subcortical Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gliosis, Familial Progressive Subcortical from the curated CTD Gene-Disease Associations dataset.
Insomnia, Fatal Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Insomnia, Fatal Familial from the curated CTD Gene-Disease Associations dataset.
SEIZURES, BENIGN FAMILIAL NEONATAL, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL NEONATAL, 2 from the curated CTD Gene-Disease Associations dataset.
Familial dermographism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial dermographism from the curated CTD Gene-Disease Associations dataset.
Candidiasis, Familial, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Candidiasis, Familial, 3 from the curated CTD Gene-Disease Associations dataset.
HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE from the curated CTD Gene-Disease Associations dataset.
Erythrocytosis, Familial, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Erythrocytosis, Familial, 3 from the curated CTD Gene-Disease Associations dataset.
Erythrocytosis, Familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Erythrocytosis, Familial, 2 from the curated CTD Gene-Disease Associations dataset.
Visceral Myopathy, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Visceral Myopathy, Familial from the curated CTD Gene-Disease Associations dataset.
Hyperthyroidism, Familial Gestational Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperthyroidism, Familial Gestational from the curated CTD Gene-Disease Associations dataset.
Hematuria, Benign Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hematuria, Benign Familial from the curated CTD Gene-Disease Associations dataset.
SEIZURES, BENIGN FAMILIAL INFANTILE, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL INFANTILE, 2 from the curated CTD Gene-Disease Associations dataset.
Febrile Convulsions, Familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 2 from the curated CTD Gene-Disease Associations dataset.
Migraine, Familial Hemiplegic, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Migraine, Familial Hemiplegic, 3 from the curated CTD Gene-Disease Associations dataset.
FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1 from the curated CTD Gene-Disease Associations dataset.
Cancer, Familial, with In Vitro Radioresistance Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cancer, Familial, with In Vitro Radioresistance from the curated CTD Gene-Disease Associations dataset.
Febrile Convulsions, Familial, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 5 from the curated CTD Gene-Disease Associations dataset.
Hypoparathyroidism familial isolated Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypoparathyroidism familial isolated from the curated CTD Gene-Disease Associations dataset.
Tumoral Calcinosis, Hyperphosphatemic, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Tumoral Calcinosis, Hyperphosphatemic, Familial from the curated CTD Gene-Disease Associations dataset.
Atrial Fibrillation, Familial, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 3 from the curated CTD Gene-Disease Associations dataset.
Hidradenitis suppurativa, familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hidradenitis suppurativa, familial from the curated CTD Gene-Disease Associations dataset.
Dementia, familial Danish Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dementia, familial Danish from the curated CTD Gene-Disease Associations dataset.
Familial medullary thyroid carcinoma Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial medullary thyroid carcinoma from the curated CTD Gene-Disease Associations dataset.
Interstitial Pneumonitis, Desquamative, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Interstitial Pneumonitis, Desquamative, Familial from the curated CTD Gene-Disease Associations dataset.
Hemophagocytic lymphohistiocytosis, familial, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hemophagocytic lymphohistiocytosis, familial, 4 from the curated CTD Gene-Disease Associations dataset.
Pseudohyperkalemia, Familial, 2, due to Red Cell Leak Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pseudohyperkalemia, Familial, 2, due to Red Cell Leak from the curated CTD Gene-Disease Associations dataset.
Cirrhosis, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cirrhosis, Familial from the curated CTD Gene-Disease Associations dataset.
Familial encephalopathy with neuroserpin inclusion bodies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial encephalopathy with neuroserpin inclusion bodies from the curated CTD Gene-Disease Associations dataset.
Lipodystrophy, Familial Partial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lipodystrophy, Familial Partial from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Restrictive, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 3 from the curated CTD Gene-Disease Associations dataset.
Familial Mediterranean Fever, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Mediterranean Fever, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Familial Hypophosphatemic Rickets Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Hypophosphatemic Rickets from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 3 from the curated CTD Gene-Disease Associations dataset.
Keratoacanthoma familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Keratoacanthoma familial from the curated CTD Gene-Disease Associations dataset.
Hepatic Adenomas, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hepatic Adenomas, Familial from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 10 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 13 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 13 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 15 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 15 from the curated CTD Gene-Disease Associations dataset.
Familial Wilms tumor 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Wilms tumor 2 from the curated CTD Gene-Disease Associations dataset.
Candidiasis, Familial, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Candidiasis, Familial, 1 from the curated CTD Gene-Disease Associations dataset.
Febrile Convulsions, Familial, 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 9 from the curated CTD Gene-Disease Associations dataset.
Hyperinsulinemic Hypoglycemia, Familial, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperinsulinemic Hypoglycemia, Familial, 4 from the curated CTD Gene-Disease Associations dataset.
Hyperinsulinemic Hypoglycemia, Familial, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperinsulinemic Hypoglycemia, Familial, 5 from the curated CTD Gene-Disease Associations dataset.
Familial antiphospholipid syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial antiphospholipid syndrome from the curated CTD Gene-Disease Associations dataset.
Amyloidosis, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Amyloidosis, Familial from the curated CTD Gene-Disease Associations dataset.
Familial paroxysmal dystonia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial paroxysmal dystonia from the curated CTD Gene-Disease Associations dataset.
Atrial fibrillation, familial 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial fibrillation, familial 1 from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, FAMILIAL TEMPORAL LOBE, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 3 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 from the curated CTD Gene-Disease Associations dataset.
Hypercholanemia, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypercholanemia, Familial from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 from the curated CTD Gene-Disease Associations dataset.
Hyperbilirubinemia, Transient Familial Neonatal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperbilirubinemia, Transient Familial Neonatal from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, FAMILIAL TEMPORAL LOBE, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 2 from the curated CTD Gene-Disease Associations dataset.
Meningioma, familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Meningioma, familial from the curated CTD Gene-Disease Associations dataset.
Aortic Aneurysm, Familial Thoracic 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 6 from the curated CTD Gene-Disease Associations dataset.
Aortic Aneurysm, Familial Thoracic 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 2 from the curated CTD Gene-Disease Associations dataset.
Dysautonomia, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dysautonomia, Familial from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 1 from the curated CTD Gene-Disease Associations dataset.
Hemophagocytic lymphohistiocytosis, familial, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hemophagocytic lymphohistiocytosis, familial, 3 from the curated CTD Gene-Disease Associations dataset.
Familial Cold Autoinflammatory Syndrome 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Cold Autoinflammatory Syndrome 2 from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Familial Adult Myoclonic, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Familial Adult Myoclonic, 3 from the curated CTD Gene-Disease Associations dataset.
Prostate cancer, familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Prostate cancer, familial from the curated CTD Gene-Disease Associations dataset.
Convulsions, Benign Familial Infantile, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Convulsions, Benign Familial Infantile, 4 from the curated CTD Gene-Disease Associations dataset.
Polycythemia, primary familial and congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Polycythemia, primary familial and congenital from the curated CTD Gene-Disease Associations dataset.
PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA from the curated CTD Gene-Disease Associations dataset.
Aortic Aneurysm, Familial Thoracic 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 1 from the curated CTD Gene-Disease Associations dataset.
Erythrocytosis, Familial, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Erythrocytosis, Familial, 4 from the curated CTD Gene-Disease Associations dataset.
Hyperinsulinemic hypoglycemia, familial, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperinsulinemic hypoglycemia, familial, 3 from the curated CTD Gene-Disease Associations dataset.
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.
Hyperinsulinemic hypoglycemia, familial, 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperinsulinemic hypoglycemia, familial, 7 from the curated CTD Gene-Disease Associations dataset.
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 from the curated CTD Gene-Disease Associations dataset.
Hyperthyroxinemia, Familial Dysalbuminemic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperthyroxinemia, Familial Dysalbuminemic from the curated CTD Gene-Disease Associations dataset.
Aortic aneurysm, familial thoracic 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic aneurysm, familial thoracic 4 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Restrictive, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 2 from the curated CTD Gene-Disease Associations dataset.
Atrial Fibrillation, Familial, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 5 from the curated CTD Gene-Disease Associations dataset.
Familial cylindromatosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial cylindromatosis from the curated CTD Gene-Disease Associations dataset.
Familial benign hypercalcemia, type 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial benign hypercalcemia, type 3 from the curated CTD Gene-Disease Associations dataset.
Hyperaldosteronism, Familial, Type II Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperaldosteronism, Familial, Type II from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 11 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 11 from the curated CTD Gene-Disease Associations dataset.
Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia from the curated CTD Gene-Disease Associations dataset.
Atrial myxoma, familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial myxoma, familial from the curated CTD Gene-Disease Associations dataset.
Tumoral Calcinosis, Normophosphatemic, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Tumoral Calcinosis, Normophosphatemic, Familial from the curated CTD Gene-Disease Associations dataset.
MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.
Hypocalciuric hypercalcemia, familial, type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypocalciuric hypercalcemia, familial, type 1 from the curated CTD Gene-Disease Associations dataset.
Trichoepithelioma multiple familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Trichoepithelioma multiple familial from the curated CTD Gene-Disease Associations dataset.
Febrile Convulsions, Familial, 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 10 from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, FAMILIAL TEMPORAL LOBE, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 1 from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2 from the curated CTD Gene-Disease Associations dataset.
Hemophagocytic lymphohistiocytosis, familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hemophagocytic lymphohistiocytosis, familial, 2 from the curated CTD Gene-Disease Associations dataset.
Periodic fever, familial, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Periodic fever, familial, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
VENTRICULAR TACHYCARDIA, FAMILIAL Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease VENTRICULAR TACHYCARDIA, FAMILIAL from the curated CTD Gene-Disease Associations dataset.
Hyperuricemic Nephropathy, Familial Juvenile 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperuricemic Nephropathy, Familial Juvenile 2 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 from the curated CTD Gene-Disease Associations dataset.
Hypobetalipoproteinemia, Familial, Apolipoprotein B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypobetalipoproteinemia, Familial, Apolipoprotein B from the curated CTD Gene-Disease Associations dataset.
Aortic Aneurysm, Familial Abdominal 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Abdominal 3 from the curated CTD Gene-Disease Associations dataset.
Familial schizencephaly Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial schizencephaly from the curated CTD Gene-Disease Associations dataset.
Atrial Fibrillation, Familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 2 from the curated CTD Gene-Disease Associations dataset.
HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1 from the curated CTD Gene-Disease Associations dataset.
Neurofibromatosis, Familial Spinal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neurofibromatosis, Familial Spinal from the curated CTD Gene-Disease Associations dataset.
Reticuloendotheliosis, familial, with eosinophilia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Reticuloendotheliosis, familial, with eosinophilia from the curated CTD Gene-Disease Associations dataset.
SEIZURES, BENIGN FAMILIAL NEONATAL, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL NEONATAL, 1 from the curated CTD Gene-Disease Associations dataset.
Advanced Sleep-Phase Syndrome, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Advanced Sleep-Phase Syndrome, Familial from the curated CTD Gene-Disease Associations dataset.
MIGRAINE, FAMILIAL HEMIPLEGIC, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MIGRAINE, FAMILIAL HEMIPLEGIC, 2 from the curated CTD Gene-Disease Associations dataset.
MIGRAINE, FAMILIAL HEMIPLEGIC, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MIGRAINE, FAMILIAL HEMIPLEGIC, 1 from the curated CTD Gene-Disease Associations dataset.
MITRAL VALVE PROLAPSE, FAMILIAL Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MITRAL VALVE PROLAPSE, FAMILIAL from the curated CTD Gene-Disease Associations dataset.
Progressive Familial Heart Block, Type Ib Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive Familial Heart Block, Type Ib from the curated CTD Gene-Disease Associations dataset.
Familial dilated cardiomyopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial dilated cardiomyopathy from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 from the curated CTD Gene-Disease Associations dataset.
Cholestasis, progressive familial intrahepatic 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 3 from the curated CTD Gene-Disease Associations dataset.
Thymoma, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thymoma, Familial from the curated CTD Gene-Disease Associations dataset.
Atypical Mycobacteriosis, Familial, X-Linked 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atypical Mycobacteriosis, Familial, X-Linked 1 from the curated CTD Gene-Disease Associations dataset.
Familial Testotoxicosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Testotoxicosis from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Myoclonic, Benign Adult Familial, Type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Myoclonic, Benign Adult Familial, Type 1 from the curated CTD Gene-Disease Associations dataset.
Hemiplegic migraine, familial type 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hemiplegic migraine, familial type 2 from the curated CTD Gene-Disease Associations dataset.
Hemiplegic migraine, familial type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hemiplegic migraine, familial type 1 from the curated CTD Gene-Disease Associations dataset.
HYPERCHOLESTEROLEMIA, FAMILIAL Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease HYPERCHOLESTEROLEMIA, FAMILIAL from the curated CTD Gene-Disease Associations dataset.
Amyloid Neuropathies, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Amyloid Neuropathies, Familial from the curated CTD Gene-Disease Associations dataset.
CANDIDIASIS, FAMILIAL, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CANDIDIASIS, FAMILIAL, 2 from the curated CTD Gene-Disease Associations dataset.
Familial Mediterranean Fever Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Mediterranean Fever from the curated CTD Gene-Disease Associations dataset.
Febrile Convulsions, Familial, 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 7 from the curated CTD Gene-Disease Associations dataset.
Febrile Convulsions, Familial, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 6 from the curated CTD Gene-Disease Associations dataset.
Febrile Convulsions, Familial, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 1 from the curated CTD Gene-Disease Associations dataset.
Cerebral Amyloid Angiopathy, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral Amyloid Angiopathy, Familial from the curated CTD Gene-Disease Associations dataset.
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12 from the curated CTD Gene-Disease Associations dataset.
Hypobetalipoproteinemia, Familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypobetalipoproteinemia, Familial, 2 from the curated CTD Gene-Disease Associations dataset.
Stuttering, Familial Persistent 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Stuttering, Familial Persistent 2 from the curated CTD Gene-Disease Associations dataset.
Trichoepithelioma, Multiple Familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Trichoepithelioma, Multiple Familial, 2 from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Familial Temporal Lobe, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Familial Temporal Lobe, 4 from the curated CTD Gene-Disease Associations dataset.
MYOCLONIC EPILEPSY, FAMILIAL INFANTILE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYOCLONIC EPILEPSY, FAMILIAL INFANTILE from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 14 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 14 from the curated CTD Gene-Disease Associations dataset.
familial mediterranean fever Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial mediterranean fever from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial adenomatous polyposis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial adenomatous polyposis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial hyperlipidemia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial hyperlipidemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial hemiplegic migraine Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial hemiplegic migraine from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial atrial fibrillation Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial atrial fibrillation from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial juvenile hyperuricemic nephropathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial juvenile hyperuricemic nephropathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial periodic paralysis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial periodic paralysis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial hypertriglyceridemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial hypertriglyceridemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign familial infantile epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign familial infantile epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial melanoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial adenomatous polyposis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial adenomatous polyposis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial combined hyperlipidemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial combined hyperlipidemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial renal oncocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial renal oncocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fatal familial insomnia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fatal familial insomnia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial mediterranean fever Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial mediterranean fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial nephrotic syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial nephrotic syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial glomangioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial glomangioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial hyperlipidemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial hyperlipidemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial hypercholesterolemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial hypercholesterolemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial periodic paralysis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial periodic paralysis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial juvenile hyperuricemic nephropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial juvenile hyperuricemic nephropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign familial neonatal epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign familial neonatal epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial partial lipodystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial partial lipodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial hemiplegic migraine Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial hemiplegic migraine in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial visceral amyloidosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial visceral amyloidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial atrial fibrillation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial atrial fibrillation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial medullary thyroid carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial medullary thyroid carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial renal papillary carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial renal papillary carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial retinoblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial retinoblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial adenomatous polyposis. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial adenomatous polyposis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; familial mediterranean fever; rheumatoid arthritis; rheumatoid spondylitis; spondylitis, ankylosing Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; familial mediterranean fever; rheumatoid arthritis; rheumatoid spondylitis; spondylitis, ankylosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperlipidemia, familial combined Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; spondylitis, ankylosing Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; spondylitis, ankylosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild familial hypercholesterolemia Gene Set From GAD Gene-Disease Associations genes associated with the disease mild familial hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial atypical progressive supranuclear palsy Gene Set From GAD Gene-Disease Associations genes associated with the disease familial atypical progressive supranuclear palsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperlipidemia, familial combined; insulin resistance; mixed hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperlipidemia, familial combined; insulin resistance; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial or sporadic prostate cancer. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial or sporadic prostate cancer. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial distal renal tubular acidosis Gene Set From GAD Gene-Disease Associations genes associated with the disease familial distal renal tubular acidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abdominal pain; amyloidosis; arthritis; familial mediterranean fever; fever Gene Set From GAD Gene-Disease Associations genes associated with the disease abdominal pain; amyloidosis; arthritis; familial mediterranean fever; fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypercholesterolemia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial defective apolipoprotein b100. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial defective apolipoprotein b100. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypercholesterolaemia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypercholesterolaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; henoch-schoenlein purpura; purpura, schoenlein-henoch Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; henoch-schoenlein purpura; purpura, schoenlein-henoch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis, familial; cerebral hemorrhage; cerebral hemorrhages Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis, familial; cerebral hemorrhage; cerebral hemorrhages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; glomerulonephritis, iga; iga glomerulonephritides Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; glomerulonephritis, iga; iga glomerulonephritides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloid neuropathies; amyloid neuropathies, familial Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloid neuropathies; amyloid neuropathies, familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
early-onset familial alzheimer's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease early-onset familial alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, juvenile rheumatoid; arthritis, psoriatic; familial mediterranean fever; Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; arthritis, psoriatic; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abdomen, acute; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease abdomen, acute; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; hyperlipidemia, familial combined Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial dysbetalipoproteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial dysbetalipoproteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial defective apolipoprotein b Gene Set From GAD Gene-Disease Associations genes associated with the disease familial defective apolipoprotein b in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial amyloid polyneuropathy. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial amyloid polyneuropathy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
parkinson's disease (familial) Gene Set From GAD Gene-Disease Associations genes associated with the disease parkinson's disease (familial) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild familial hypercholesterolaemia Gene Set From GAD Gene-Disease Associations genes associated with the disease mild familial hypercholesterolaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial combined hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial combined hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
endogenous hypertriglyceridemia and familial hypercholesterolemia Gene Set From GAD Gene-Disease Associations genes associated with the disease endogenous hypertriglyceridemia and familial hypercholesterolemia 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 Set From 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.
familial type 3 hyperlipoproteinaemia; hyperlipoproteinemia type iii Gene Set From GAD Gene-Disease Associations genes associated with the disease familial type 3 hyperlipoproteinaemia; hyperlipoproteinemia type iii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial age-related macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease familial age-related macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial premature myocardial infarction. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial premature myocardial infarction. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
late onset of familial adenomatous polyposis Gene Set From GAD Gene-Disease Associations genes associated with the disease late onset of familial adenomatous polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial amyloidotic polyneuropathy. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial amyloidotic polyneuropathy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloid neuropathies, familial Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloid neuropathies, familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperlipidemia, familial combined; mixed hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperlipidemia, familial combined; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
colitis, ulcerative; crohn disease; familial mediterranean fever; inflammatory bowel diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease colitis, ulcerative; crohn disease; familial mediterranean fever; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial defective apolipoprotein b-100 in a chinese man Gene Set From GAD Gene-Disease Associations genes associated with the disease familial defective apolipoprotein b-100 in a chinese man in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; familial mediterranean fever; tuberculosis, pulmonary Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; familial mediterranean fever; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
premature coronary artery disease and familial hypoalphalipoproteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease premature coronary artery disease and familial hypoalphalipoproteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; familial mediterranean fever; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; familial mediterranean fever; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial male-limited precocious puberty. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial male-limited precocious puberty. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial combined hyperlipidaemia. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial combined hyperlipidaemia. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; familial mediterranean fever; inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; familial mediterranean fever; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fam hyperbetalipoproteinaemia; hyperlipidemia, familial combined; hyperlipoproteinemia type ii; hypertriglyceridemia; mixed hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease fam hyperbetalipoproteinaemia; hyperlipidemia, familial combined; hyperlipoproteinemia type ii; hypertriglyceridemia; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial early onset psoriasis. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial early onset psoriasis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypobetalipoproteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypobetalipoproteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial amyotrophic lateral sclerosis. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial amyotrophic lateral sclerosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial amyloid polyneuropathy in a hungarian family. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial amyloid polyneuropathy in a hungarian family. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial melanoma Gene Set From GAD Gene-Disease Associations genes associated with the disease familial melanoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
rapidly progressive familial amyotrophic lateral sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease rapidly progressive familial amyotrophic lateral sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial amyotrophic lateral sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease familial amyotrophic lateral sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, juvenile rheumatoid; familial mediterranean fever; Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; coronary artery disease; hyperlipidemia, familial combined; mixed hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; coronary artery disease; hyperlipidemia, familial combined; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypocalciuric hypercalcemia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypocalciuric hypercalcemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial adenomatous polyposis Gene Set From GAD Gene-Disease Associations genes associated with the disease familial adenomatous polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hyperinsulinism. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hyperinsulinism. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
late onset familial adenomatous polyposis Gene Set From GAD Gene-Disease Associations genes associated with the disease late onset familial adenomatous polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial amyloid polyneuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease familial amyloid polyneuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypercholesterolemia. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypercholesterolemia. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial partial lipodystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease familial partial lipodystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial amyloidotic polyneuropathy type 1 Gene Set From GAD Gene-Disease Associations genes associated with the disease familial amyloidotic polyneuropathy type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; infertility, male Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial liver adenomatosis Gene Set From GAD Gene-Disease Associations genes associated with the disease familial liver adenomatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diarrhea; familial mediterranean fever; pain; stomatitis, aphthous Gene Set From GAD Gene-Disease Associations genes associated with the disease diarrhea; familial mediterranean fever; pain; stomatitis, aphthous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
breast cancer, familial Gene Set From GAD Gene-Disease Associations genes associated with the disease breast cancer, familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; hyperlipidemia, familial combined Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypertrophic cardiomyopathy. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypertrophic cardiomyopathy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial cataract Gene Set From GAD Gene-Disease Associations genes associated with the disease familial cataract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloid neuropathies, familial; constipation; diarrhea; gastrointestinal diseases; nausea; vomiting Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloid neuropathies, familial; constipation; diarrhea; gastrointestinal diseases; nausea; vomiting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; arthritis, rheumatoid; familial mediterranean fever; Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; arthritis, rheumatoid; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; hyperlipidemia, familial combined; metabolic syndrome x; mixed hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; hyperlipidemia, familial combined; metabolic syndrome x; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
creutzfeldt-jakob disease; creutzfeldt-jakob syndrome; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease creutzfeldt-jakob disease; creutzfeldt-jakob syndrome; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood pressure; hyperlipidemia, familial combined Gene Set From GAD Gene-Disease Associations genes associated with the disease blood pressure; hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; atherosclerosis; familial mediterranean fever; Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; atherosclerosis; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
creutzfeldt-jakob disease; gerstmann-straussler-scheinker disease; insomnia, fatal familial Gene Set From GAD Gene-Disease Associations genes associated with the disease creutzfeldt-jakob disease; gerstmann-straussler-scheinker disease; insomnia, fatal familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial exudative vitreoretinopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease familial exudative vitreoretinopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic, familial Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic, familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; arthritis, rheumatoid; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; arthritis, rheumatoid; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial dysautonomia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial dysautonomia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial alzheimer's disease associated Gene Set From GAD Gene-Disease Associations genes associated with the disease familial alzheimer's disease associated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial spondyloepiphyseal dysplasia tarda, brachydactyly, and precocious osteoarthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease familial spondyloepiphyseal dysplasia tarda, brachydactyly, and precocious osteoarthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
greenland familial cholestasis Gene Set From GAD Gene-Disease Associations genes associated with the disease greenland familial cholestasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial diabetes insipidus Gene Set From GAD Gene-Disease Associations genes associated with the disease familial diabetes insipidus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial erythrocytosis Gene Set From GAD Gene-Disease Associations genes associated with the disease familial erythrocytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial bronchiectasis. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial bronchiectasis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, juvenile rheumatoid; chronic childhood arthritis; familial mediterranean fever; inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; chronic childhood arthritis; familial mediterranean fever; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial non-ret c cell hyperplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial non-ret c cell hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypertension of early onset. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypertension of early onset. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; hyperlipidemia, familial combined Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; hyper-igd syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; hyper-igd syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; fever Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term familial in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Familial combined hyperlipidaemia_Blood monocyte_GSE11393 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Familial combined hyperlipidaemia_Blood monocyte_GSE11393 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Familial combined hyperlipidaemia_lymphoblast_GSE1010 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Familial combined hyperlipidaemia_lymphoblast_GSE1010 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Familial hypophosphataemic rickets_Renal Tissue_GSE868 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Familial hypophosphataemic rickets_Renal Tissue_GSE868 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Parkinson's disease (familial) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Parkinson's disease (familial) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
familial hypertriglyceridemia Gene Set From GWASdb SNP-Disease Associations genes associated with the disease familial hypertriglyceridemia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
familial atrial fibrillation Gene Set From GWASdb SNP-Disease Associations genes associated with the disease familial atrial fibrillation in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
familial predisposition Gene Set From HPO Gene-Disease Associations genes associated with the familial predisposition phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Hyperlipidemia, Familial Combined Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hyperlipidemia, Familial Combined phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Paralyses, Familial Periodic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Paralyses, Familial Periodic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cardiomyopathy, Hypertrophic, Familial Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cardiomyopathy, Hypertrophic, Familial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Familial Mediterranean Fever Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Familial Mediterranean Fever phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Lipodystrophy, Familial Partial Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Lipodystrophy, Familial Partial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Amyloidosis, Familial Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Amyloidosis, Familial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Dysautonomia, Familial Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Dysautonomia, Familial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Amyloid Neuropathies, Familial Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Amyloid Neuropathies, Familial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Insomnia, Fatal Familial Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Insomnia, Fatal Familial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
epilepsy, familial focal, with variable foci Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, familial focal, with variable foci phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperparathyroidism, familial primary Gene Set From OMIM Gene-Disease Associations genes associated with the hyperparathyroidism, familial primary phenotype from the curated OMIM Gene-Disease Associations dataset.
{atrial fibrillation, familial, 5} Gene Set From OMIM Gene-Disease Associations genes associated with the {atrial fibrillation, familial, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.
{breast-ovarian cancer, familial, 1} Gene Set From OMIM Gene-Disease Associations genes associated with the {breast-ovarian cancer, familial, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.
digital arthropathy-brachydactyly, familial Gene Set From OMIM Gene-Disease Associations genes associated with the digital arthropathy-brachydactyly, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive familial heart block, type ib Gene Set From OMIM Gene-Disease Associations genes associated with the progressive familial heart block, type ib phenotype from the curated OMIM Gene-Disease Associations dataset.
migraine, familial basilar Gene Set From OMIM Gene-Disease Associations genes associated with the migraine, familial basilar phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 4 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 6 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 7 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 1 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 2 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 8 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 9 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
insomnia, fatal familial Gene Set From OMIM Gene-Disease Associations genes associated with the insomnia, fatal familial phenotype from the curated OMIM Gene-Disease Associations dataset.
dysautonomia, familial Gene Set From OMIM Gene-Disease Associations genes associated with the dysautonomia, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 9 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 8 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
combined hyperlipidemia, familial Gene Set From OMIM Gene-Disease Associations genes associated with the combined hyperlipidemia, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial abdominal 1 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial abdominal 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial abdominal 2 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial abdominal 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
familial cold-induced inflammatory syndrome 1 Gene Set From OMIM Gene-Disease Associations genes associated with the familial cold-induced inflammatory syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 11 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 10 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, familial temporal lobe, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, familial temporal lobe, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, familial temporal lobe, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, familial temporal lobe, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, familial temporal lobe, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, familial temporal lobe, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, familial temporal lobe, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, familial temporal lobe, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, familial temporal lobe, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, familial temporal lobe, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 19 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 19 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 18 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 18 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 11 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 10 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 13 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 12 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 15 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 15 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 14 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 16 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 16 phenotype from the curated OMIM Gene-Disease Associations dataset.
hypobetalipoproteinemia, familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the hypobetalipoproteinemia, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 3a Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 3a phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic 17 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic 17 phenotype from the curated OMIM Gene-Disease Associations dataset.
dementia, familial danish Gene Set From OMIM Gene-Disease Associations genes associated with the dementia, familial danish phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic 6 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign familial infantile, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign familial infantile, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign familial infantile, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign familial infantile, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperuricemic nephropathy, familial juvenile 1 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperuricemic nephropathy, familial juvenile 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
{breast-ovarian cancer, familial, susceptibility to, 4} Gene Set From OMIM Gene-Disease Associations genes associated with the {breast-ovarian cancer, familial, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperaldosteronism, familial, type iii Gene Set From OMIM Gene-Disease Associations genes associated with the hyperaldosteronism, familial, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperinsulinemic hypoglycemia, familial, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperinsulinemic hypoglycemia, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperinsulinemic hypoglycemia, familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperinsulinemic hypoglycemia, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperinsulinemic hypoglycemia, familial, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperinsulinemic hypoglycemia, familial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperinsulinemic hypoglycemia, familial, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperinsulinemic hypoglycemia, familial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperinsulinemic hypoglycemia, familial, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperinsulinemic hypoglycemia, familial, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperinsulinemic hypoglycemia, familial, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperinsulinemic hypoglycemia, familial, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
?epilepsy, familial adult myoclonic, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the ?epilepsy, familial adult myoclonic, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
?candidiasis, familial, 8 Gene Set From OMIM Gene-Disease Associations genes associated with the ?candidiasis, familial, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
[fleck retina, familial benign] Gene Set From OMIM Gene-Disease Associations genes associated with the [fleck retina, familial benign] phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 21 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 21 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 22 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 22 phenotype from the curated OMIM Gene-Disease Associations dataset.
candidiasis, familial, 6, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the candidiasis, familial, 6, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
carpal tunnel syndrome, familial Gene Set From OMIM Gene-Disease Associations genes associated with the carpal tunnel syndrome, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 13 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 12 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 11 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 10 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 17 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 17 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 16 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 16 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 14 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
medullary thyroid carcinoma, familial Gene Set From OMIM Gene-Disease Associations genes associated with the medullary thyroid carcinoma, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
hypercholesterolemia, familial, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the hypercholesterolemia, familial, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
ventricular fibrillation, paroxysmal familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ventricular fibrillation, paroxysmal familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 9 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 8 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
acne inversa, familial, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the acne inversa, familial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
endometrial cancer, familial Gene Set From OMIM Gene-Disease Associations genes associated with the endometrial cancer, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperbilirubinemia, familial transient neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the hyperbilirubinemia, familial transient neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
dementia, familial, nonspecific Gene Set From OMIM Gene-Disease Associations genes associated with the dementia, familial, nonspecific phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperuricemic nephropathy, familial juvenile 2 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperuricemic nephropathy, familial juvenile 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperuricemic nephropathy, familial juvenile, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperuricemic nephropathy, familial juvenile, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperaldosteronism, familial, type ii Gene Set From OMIM Gene-Disease Associations genes associated with the hyperaldosteronism, familial, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.
lipodystrophy, familial partial, type 4 Gene Set From OMIM Gene-Disease Associations genes associated with the lipodystrophy, familial partial, type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
lipodystrophy, familial partial, type 3 Gene Set From OMIM Gene-Disease Associations genes associated with the lipodystrophy, familial partial, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
hemophagocytic lymphohistiocytosis, familial, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the hemophagocytic lymphohistiocytosis, familial, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
hemophagocytic lymphohistiocytosis, familial, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the hemophagocytic lymphohistiocytosis, familial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
amyloidosis, familial visceral Gene Set From OMIM Gene-Disease Associations genes associated with the amyloidosis, familial visceral phenotype from the curated OMIM Gene-Disease Associations dataset.
migraine, familial hemiplegic, 1, with progressive cerebellar ataxia Gene Set From OMIM Gene-Disease Associations genes associated with the migraine, familial hemiplegic, 1, with progressive cerebellar ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.
hematuria, familial benign Gene Set From OMIM Gene-Disease Associations genes associated with the hematuria, familial benign phenotype from the curated OMIM Gene-Disease Associations dataset.
hematuria, benign familial Gene Set From OMIM Gene-Disease Associations genes associated with the hematuria, benign familial phenotype from the curated OMIM Gene-Disease Associations dataset.
dementia, familial british Gene Set From OMIM Gene-Disease Associations genes associated with the dementia, familial british phenotype from the curated OMIM Gene-Disease Associations dataset.
pseudohyperkalemia, familial, 2, due to red cell leak Gene Set From OMIM Gene-Disease Associations genes associated with the pseudohyperkalemia, familial, 2, due to red cell leak phenotype from the curated OMIM Gene-Disease Associations dataset.
myasthenia, limb-girdle, familial Gene Set From OMIM Gene-Disease Associations genes associated with the myasthenia, limb-girdle, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
hemophagocytic lymphohistiocytosis, familial, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the hemophagocytic lymphohistiocytosis, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
hemophagocytic lymphohistiocytosis, familial, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the hemophagocytic lymphohistiocytosis, familial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
[erythrocytosis, familial, 1] Gene Set From OMIM Gene-Disease Associations genes associated with the [erythrocytosis, familial, 1] phenotype from the curated OMIM Gene-Disease Associations dataset.
encephalopathy, familial, with neuroserpin inclusion bodies Gene Set From OMIM Gene-Disease Associations genes associated with the encephalopathy, familial, with neuroserpin inclusion bodies phenotype from the curated OMIM Gene-Disease Associations dataset.
{migraine, familial typical, susceptibility to, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {migraine, familial typical, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperpigmentation, familial progressive, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperpigmentation, familial progressive, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive familial intrahepatic 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive familial intrahepatic 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive familial intrahepatic 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive familial intrahepatic 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive familial intrahepatic 3 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive familial intrahepatic 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive familial intrahepatic 4 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive familial intrahepatic 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
pulmonary hypertension, familial primary, 1, with or without hht Gene Set From OMIM Gene-Disease Associations genes associated with the pulmonary hypertension, familial primary, 1, with or without hht phenotype from the curated OMIM Gene-Disease Associations dataset.
thrombophilia, familial, due to decreased release of plat Gene Set From OMIM Gene-Disease Associations genes associated with the thrombophilia, familial, due to decreased release of plat phenotype from the curated OMIM Gene-Disease Associations dataset.
cylindromatosis, familial Gene Set From OMIM Gene-Disease Associations genes associated with the cylindromatosis, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
dyskinesia, familial, with facial myokymia Gene Set From OMIM Gene-Disease Associations genes associated with the dyskinesia, familial, with facial myokymia phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic pain syndrome, familial, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the episodic pain syndrome, familial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic pain syndrome, familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the episodic pain syndrome, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
hypoparathyroidism, familial isolated Gene Set From OMIM Gene-Disease Associations genes associated with the hypoparathyroidism, familial isolated phenotype from the curated OMIM Gene-Disease Associations dataset.
gastrointestinal stromal tumor, familial Gene Set From OMIM Gene-Disease Associations genes associated with the gastrointestinal stromal tumor, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
{aneurysm, familial abdominal 3} Gene Set From OMIM Gene-Disease Associations genes associated with the {aneurysm, familial abdominal 3} phenotype from the curated OMIM Gene-Disease Associations dataset.
hemophagocytic lymphohistiocytosis, familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the hemophagocytic lymphohistiocytosis, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 3b Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 3b phenotype from the curated OMIM Gene-Disease Associations dataset.
{hypercholesterolemia, familial, due to ldlr defect, modifier of} Gene Set From OMIM Gene-Disease Associations genes associated with the {hypercholesterolemia, familial, due to ldlr defect, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.
advanced sleep phase syndrome, familial, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the advanced sleep phase syndrome, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
stuttering, familial persistent, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the stuttering, familial persistent, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
stuttering, familial persistent, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the stuttering, familial persistent, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
stuttering, familial persistent, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the stuttering, familial persistent, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
stuttering, familial persistent, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the stuttering, familial persistent, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
erythrocytosis, familial, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the erythrocytosis, familial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
erythrocytosis, familial, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the erythrocytosis, familial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
erythrocytosis, familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the erythrocytosis, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
hypercholesterolemia, familial, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the hypercholesterolemia, familial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
x inactivation, familial skewed, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the x inactivation, familial skewed, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
{breast-ovarian cancer, familial, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {breast-ovarian cancer, familial, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial restrictive, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial restrictive, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial restrictive, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial restrictive, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial restrictive, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial restrictive, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial restrictive, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial restrictive, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
candidiasis, familial, 5, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the candidiasis, familial, 5, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
hypercholanemia, familial Gene Set From OMIM Gene-Disease Associations genes associated with the hypercholanemia, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
candidiasis, familial, 4, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the candidiasis, familial, 4, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
myasthenia, familial infantile, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the myasthenia, familial infantile, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
{prostate cancer, familial, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {prostate cancer, familial, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic pain syndrome, familial Gene Set From OMIM Gene-Disease Associations genes associated with the episodic pain syndrome, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
familial mediterranean fever, ar Gene Set From OMIM Gene-Disease Associations genes associated with the familial mediterranean fever, ar phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, familial adult myoclonic, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, familial adult myoclonic, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
gastric cancer, familial diffuse, with or without cleft lip and/or palate Gene Set From OMIM Gene-Disease Associations genes associated with the gastric cancer, familial diffuse, with or without cleft lip and/or palate phenotype from the curated OMIM Gene-Disease Associations dataset.
lipodystrophy, familial partial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the lipodystrophy, familial partial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
{coronary artery disease in familial hypercholesterolemia, protection against} Gene Set From OMIM Gene-Disease Associations genes associated with the {coronary artery disease in familial hypercholesterolemia, protection against} phenotype from the curated OMIM Gene-Disease Associations dataset.
thrombotic thrombocytopenic purpura, familial Gene Set From OMIM Gene-Disease Associations genes associated with the thrombotic thrombocytopenic purpura, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
osteolysis, familial expansile Gene Set From OMIM Gene-Disease Associations genes associated with the osteolysis, familial expansile phenotype from the curated OMIM Gene-Disease Associations dataset.
myoclonic epilepsy, infantile, familial Gene Set From OMIM Gene-Disease Associations genes associated with the myoclonic epilepsy, infantile, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
hypercholesterolemia, familial Gene Set From OMIM Gene-Disease Associations genes associated with the hypercholesterolemia, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
[gamma-glutamyltransferase, familial high serum] Gene Set From OMIM Gene-Disease Associations genes associated with the [gamma-glutamyltransferase, familial high serum] phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic phenotype from the curated OMIM Gene-Disease Associations dataset.
{breast-ovarian cancer, familial, susceptibility to, 3} Gene Set From OMIM Gene-Disease Associations genes associated with the {breast-ovarian cancer, familial, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.
acne inversa, familial, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the acne inversa, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 9 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 8 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
ectopia lentis, familial Gene Set From OMIM Gene-Disease Associations genes associated with the ectopia lentis, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
platelet disorder, familial, with associated myeloid malignancy Gene Set From OMIM Gene-Disease Associations genes associated with the platelet disorder, familial, with associated myeloid malignancy phenotype from the curated OMIM Gene-Disease Associations dataset.
cutaneous telangiectasia and cancer syndrome, familial Gene Set From OMIM Gene-Disease Associations genes associated with the cutaneous telangiectasia and cancer syndrome, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
neurofibromatosis, familial spinal Gene Set From OMIM Gene-Disease Associations genes associated with the neurofibromatosis, familial spinal phenotype from the curated OMIM Gene-Disease Associations dataset.
?familial cold autoinflammatory syndrome 4 Gene Set From OMIM Gene-Disease Associations genes associated with the ?familial cold autoinflammatory syndrome 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
renal cell carcinoma, papillary, 1, familial and somatic Gene Set From OMIM Gene-Disease Associations genes associated with the renal cell carcinoma, papillary, 1, familial and somatic phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 20 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 20 phenotype from the curated OMIM Gene-Disease Associations dataset.
tumoral calcinosis, familial, normophosphatemic Gene Set From OMIM Gene-Disease Associations genes associated with the tumoral calcinosis, familial, normophosphatemic phenotype from the curated OMIM Gene-Disease Associations dataset.
?antiphospholipid syndrome, familial Gene Set From OMIM Gene-Disease Associations genes associated with the ?antiphospholipid syndrome, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
{hyperlipidemia, familial combined, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {hyperlipidemia, familial combined, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
tumoral calcinosis, hyperphosphatemic, familial Gene Set From OMIM Gene-Disease Associations genes associated with the tumoral calcinosis, hyperphosphatemic, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia, familial, 13 Gene Set From OMIM Gene-Disease Associations genes associated with the arrhythmogenic right ventricular dysplasia, familial, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
familial mediterranean fever, ad Gene Set From OMIM Gene-Disease Associations genes associated with the familial mediterranean fever, ad phenotype from the curated OMIM Gene-Disease Associations dataset.
ventricular fibrillation, familial, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the ventricular fibrillation, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
migraine, familial hemiplegic, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the migraine, familial hemiplegic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
migraine, familial hemiplegic, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the migraine, familial hemiplegic, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
migraine, familial hemiplegic, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the migraine, familial hemiplegic, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
goiter, familial, due to ttf-1 defect Gene Set From OMIM Gene-Disease Associations genes associated with the goiter, familial, due to ttf-1 defect phenotype from the curated OMIM Gene-Disease Associations dataset.
advanced sleep-phase syndrome, familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the advanced sleep-phase syndrome, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
{meningioma, familial, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {meningioma, familial, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, myoclonic, familial adult, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, myoclonic, familial adult, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
?lipodystrophy, familial partial, type 5 Gene Set From OMIM Gene-Disease Associations genes associated with the ?lipodystrophy, familial partial, type 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
hypocalciuric hypercalcemia, familial, type iii Gene Set From OMIM Gene-Disease Associations genes associated with the hypocalciuric hypercalcemia, familial, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.
short stature, idiopathic familial Gene Set From OMIM Gene-Disease Associations genes associated with the short stature, idiopathic familial phenotype from the curated OMIM Gene-Disease Associations dataset.
candidiasis, familial, 1, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the candidiasis, familial, 1, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
periodic fever, familial Gene Set From OMIM Gene-Disease Associations genes associated with the periodic fever, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperfibrinolysis, familial, due to increased release of plat Gene Set From OMIM Gene-Disease Associations genes associated with the hyperfibrinolysis, familial, due to increased release of plat phenotype from the curated OMIM Gene-Disease Associations dataset.
{hypercholesterolemia, familial, modifier of} Gene Set From OMIM Gene-Disease Associations genes associated with the {hypercholesterolemia, familial, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperthyroidism, familial gestational Gene Set From OMIM Gene-Disease Associations genes associated with the hyperthyroidism, familial gestational phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial abdominal, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial abdominal, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
migraine, familial hemiplegic Gene Set From OMIM Gene-Disease Associations genes associated with the migraine, familial hemiplegic phenotype from the curated OMIM Gene-Disease Associations dataset.
alzheimer disease 1, familial Gene Set From OMIM Gene-Disease Associations genes associated with the alzheimer disease 1, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperproinsulinemia, familial, with or without diabetes Gene Set From OMIM Gene-Disease Associations genes associated with the hyperproinsulinemia, familial, with or without diabetes phenotype from the curated OMIM Gene-Disease Associations dataset.
vestibulopathy, familial Gene Set From OMIM Gene-Disease Associations genes associated with the vestibulopathy, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
eosinophilia, familial Gene Set From OMIM Gene-Disease Associations genes associated with the eosinophilia, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
candidiasis, familial, 2, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the candidiasis, familial, 2, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
x-inactivation, familial skewed Gene Set From OMIM Gene-Disease Associations genes associated with the x-inactivation, familial skewed phenotype from the curated OMIM Gene-Disease Associations dataset.
familial cold autoinflammatory syndrome 3 Gene Set From OMIM Gene-Disease Associations genes associated with the familial cold autoinflammatory syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
convulsions, familial infantile, with paroxysmal choreoathetosis Gene Set From OMIM Gene-Disease Associations genes associated with the convulsions, familial infantile, with paroxysmal choreoathetosis phenotype from the curated OMIM Gene-Disease Associations dataset.
trichoepithelioma, multiple familial, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the trichoepithelioma, multiple familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
trichoepithelioma, multiple familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the trichoepithelioma, multiple familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
myoclonus, familial cortical Gene Set From OMIM Gene-Disease Associations genes associated with the myoclonus, familial cortical phenotype from the curated OMIM Gene-Disease Associations dataset.
acne inversa, familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the acne inversa, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
familial cold autoinflammatory syndrome 2 Gene Set From OMIM Gene-Disease Associations genes associated with the familial cold autoinflammatory syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
Familial (Fpah) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial (Fpah) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Alzheimer Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Alzheimer Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Lichen Amyloidosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Lichen Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Breast Cancer, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Breast Cancer, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Hypercholesterolemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hypercholesterolemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypercholesterolemia, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypercholesterolemia, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypoalphalipoproteinemia, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypoalphalipoproteinemia, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nuchal Bleb, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nuchal Bleb, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Exudative Vitreoretinopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Exudative Vitreoretinopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Mediterranean Fever Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Mediterranean Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Intrahepatic Cholestasis Of Pregnancy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Intrahepatic Cholestasis Of Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Creutzfeldt-Jakob Disease, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Creutzfeldt-Jakob Disease, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Periodic Paralysis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Periodic Paralysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Primary Gastric Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Primary Gastric Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Pseudohyperkalemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Pseudohyperkalemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fatal Familial Insomnia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fatal Familial Insomnia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pseudohyperkalemia, Familial, 2, Due To Red Cell Leak Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pseudohyperkalemia, Familial, 2, Due To Red Cell Leak in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Dilated Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Dilated Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypoadrenocorticism, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypoadrenocorticism, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Thrombocytosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Thrombocytosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Osteochondritis Dissecans Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Osteochondritis Dissecans in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Generalized Lipodystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Generalized Lipodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Atypical Mole Melanoma Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Atypical Mole Melanoma Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Neurocardiogenic Syncope Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Neurocardiogenic Syncope in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Vesicoureteral Reflux Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Vesicoureteral Reflux in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Olivopontocerebellar Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Olivopontocerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Benign Hypercalcemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Benign Hypercalcemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Thoracic Aortic Aneurysm And Aortic Dissection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Thoracic Aortic Aneurysm And Aortic Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Benign Pemphigus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Benign Pemphigus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Cerebral Amyloid Angiopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Cerebral Amyloid Angiopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Hypophosphatemic Rickets Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hypophosphatemic Rickets in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Visceral Myopathy, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Visceral Myopathy, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dysautonomia, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dysautonomia, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Paroxysmal Familial Ventricular Fibrillation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Paroxysmal Familial Ventricular Fibrillation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Hematuria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hematuria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Primary Pulmonary Hypertension Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Primary Pulmonary Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Pulmonary Arterial Hypertension Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Pulmonary Arterial Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Multiple Trichoepitheliomata Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Trichoepitheliomata in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atypical Mycobacteriosis, Familial, X-Linked 1 (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atypical Mycobacteriosis, Familial, X-Linked 1 (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Epilepsies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Epilepsies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Thrombotic Thrombocytopenic Purpura Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Thrombotic Thrombocytopenic Purpura in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Ectopia Lentis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Ectopia Lentis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Idiopathic Hypercalciuria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Idiopathic Hypercalciuria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chorea, Benign Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chorea, Benign Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dyskinesia, Familial, With Facial Myokymia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dyskinesia, Familial, With Facial Myokymia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Dermographism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Dermographism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Aplasia Of The Vermis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Aplasia Of The Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Partial Lipodystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Partial Lipodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Adenomatous Polyposis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Adenomatous Polyposis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Progressive Myoclonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Progressive Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Hyperaldosteronism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hyperaldosteronism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Sick Sinus Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Sick Sinus Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Patent Ductus Arteriosus Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Patent Ductus Arteriosus Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Guillain-Barre Syndrome, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Guillain-Barre Syndrome, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Acromegaly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Acromegaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Non-Medullary Thyroid Cancer Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Non-Medullary Thyroid Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Somatotrophinoma, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Somatotrophinoma, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Intestinal Polyposis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Intestinal Polyposis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Danish Type Familial Amyloid Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Danish Type Familial Amyloid Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Juvenile Parkinsonism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Juvenile Parkinsonism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Familial Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Familial Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Familial Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anhidrosis, Familial Generalized, With Abnormal Or Absent Sweat Glands Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anhidrosis, Familial Generalized, With Abnormal Or Absent Sweat Glands in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Hypobetalipoproteinemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hypobetalipoproteinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypobetalipoproteinemia, Familial, 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypobetalipoproteinemia, Familial, 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Chondrocalcinosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Chondrocalcinosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Platelet Disorder, Familial, With Associated Myeloid Malignancy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Platelet Disorder, Familial, With Associated Myeloid Malignancy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Gigantiform Cementoma, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Gigantiform Cementoma, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Nonmedullary Thyroid Gland Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Nonmedullary Thyroid Gland Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Medullary Thyroid Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Medullary Thyroid Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Hyperparathyroidism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hyperparathyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Atypical Multiple Mole-Melanoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Atypical Multiple Mole-Melanoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dementia, Familial Danish Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dementia, Familial Danish in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Hyperalphalipoproteinemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hyperalphalipoproteinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hyperchylomicronemia With Hyperprebetalipoproteinemia, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hyperchylomicronemia With Hyperprebetalipoproteinemia, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypercholesterolemia, Familial, Due To Ligand-Defective Apolipoprotein B Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypercholesterolemia, Familial, Due To Ligand-Defective Apolipoprotein B in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypobetalipoproteinemia, Familial, Apolipoprotein B Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypobetalipoproteinemia, Familial, Apolipoprotein B in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Amyloid Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Amyloid Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Dementia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Dementia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Testicular Germ Cell Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Testicular Germ Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Motor Neuron Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Motor Neuron Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Cervical Artery Dissection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Cervical Artery Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Erythrocytosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Erythrocytosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Collagenosis, Familial Reactive Perforating Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Collagenosis, Familial Reactive Perforating in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Tremor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Tremor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Adult Familial Myoclonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Adult Familial Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Idiopathic Pulmonary Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Idiopathic Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Benign Neonatal Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Benign Neonatal Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Hemiplegic Migraine Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hemiplegic Migraine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Migraine Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Migraine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cutaneous Telangiectasia And Cancer Syndrome, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cutaneous Telangiectasia And Cancer Syndrome, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Alcoholism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Alcoholism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Central Diabetes Insipidus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Central Diabetes Insipidus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypercholanemia, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypercholanemia, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Renal Cell Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Renal Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Nonmedullary Thyroid Cancer Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Nonmedullary Thyroid Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dermatitis Herpetiformis, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dermatitis Herpetiformis, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Colorectal Camcer Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Colorectal Camcer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Hypertrophic Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hypertrophic Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Breast Cancer, Familial Male Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Breast Cancer, Familial Male in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Malignant Neoplasm Of Pancreas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Malignant Neoplasm Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Testotoxicosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Testotoxicosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hematuria, Benign Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hematuria, Benign Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Non-Familial Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Non-Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Ventricular Tachycardia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Ventricular Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Hemolytic Uremic Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hemolytic Uremic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Psoriasis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Psoriasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Pityriasis Rubra Pilaris Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Pityriasis Rubra Pilaris in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Candidiasis, Familial, 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Candidiasis, Familial, 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Cold Urticaria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Cold Urticaria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Isolated Hyperparathyroidism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Isolated Hyperparathyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Eosinophilia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Eosinophilia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Cerebral Cavernous Malformation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Cerebral Cavernous Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Atypical Hemolytic Uremic Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Atypical Hemolytic Uremic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Chronic Lymphocytic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Chronic Lymphocytic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Malignant Melanoma Of Skin Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Malignant Melanoma Of Skin in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Acute Myeloid Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Acute Myeloid Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Retinoblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Retinoblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Infantile Myasthenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Infantile Myasthenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Charge Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Charge Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Familial Convulsion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Familial Convulsion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myasthenia, Familial Infantile, 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myasthenia, Familial Infantile, 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Advanced Sleep-Phase Syndrome, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Advanced Sleep-Phase Syndrome, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Primary Hypomagnesemia With Normocalciuria And Normocalcemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Primary Hypomagnesemia With Normocalciuria And Normocalcemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Schizencephaly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Schizencephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Vascular Leukoencephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Vascular Leukoencephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Familial Mesial Temporal Lobe Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Familial Mesial Temporal Lobe Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Multiple Lipomatosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Lipomatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atypical Mycobacteriosis, Familial, X-Linked 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atypical Mycobacteriosis, Familial, X-Linked 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Amyloid Polyneuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Amyloid Polyneuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Hypoaldosteronism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hypoaldosteronism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Mitral Valve Prolapse Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Mitral Valve Prolapse in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reticuloendotheliosis, Familial, With Eosinophilia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reticuloendotheliosis, Familial, With Eosinophilia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Temporal Epilepsy, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Temporal Epilepsy, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Noncompaction Of Left Ventricular Myocardium, Familial Isolated, Autosomal Dominant 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Noncompaction Of Left Ventricular Myocardium, Familial Isolated, Autosomal Dominant 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Dyshormonogenetic Goiter Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Dyshormonogenetic Goiter in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Thyroid Dyshormonogenesis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Thyroid Dyshormonogenesis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hidradenitis Suppurativa, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hidradenitis Suppurativa, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Polycythemia Vera Gene Set From 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.
Polyneuropathy, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyneuropathy, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Lambdoid Synostosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Lambdoid Synostosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Premature Ovarian Failure, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Premature Ovarian Failure, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Antiphospholipid Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Antiphospholipid Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Hypophosphatemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hypophosphatemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Isolated Trichomegaly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Isolated Trichomegaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Acanthosis Nigricans Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Acanthosis Nigricans in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Multiple Trichodiscomas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Trichodiscomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Spontaneous Pneumothorax Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Spontaneous Pneumothorax in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Restrictive Cardiomyopathy (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Restrictive Cardiomyopathy (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dandy-Walker Syndrome, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dandy-Walker Syndrome, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ovarian Hyperstimulation Syndrome, Familial Gestational Spontaneous Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ovarian Hyperstimulation Syndrome, Familial Gestational Spontaneous in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Acute Myeloid Leukemia With Mutated Cebpa Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Acute Myeloid Leukemia With Mutated Cebpa in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Bicuspid Aortic Valve Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Bicuspid Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophia Maculosa Varioliformis Cutis, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophia Maculosa Varioliformis Cutis, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Primary Familial Brain Calcification Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Primary Familial Brain Calcification in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Hyperekplexia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hyperekplexia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nevi Flammei, Familial Multiple Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nevi Flammei, Familial Multiple in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hyperpotassemia And Hypertension, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hyperpotassemia And Hypertension, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Eunuchoidism, Familial Hypogonadotropic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Eunuchoidism, Familial Hypogonadotropic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Extrahepatic Biliary Atresia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Extrahepatic Biliary Atresia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Porphyria Cutanea Tarda Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Porphyria Cutanea Tarda in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Renal Hypouricemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Renal Hypouricemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hepatic Adenomas, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Adenomas, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Harmonizome 3.0

familial glucocorticoid deficiency Gene Set

Familial Glucocorticoid Deficiency Gene Set

Familial glucocorticoid deficiency Gene Set

Familial glucocorticoid deficiency Gene Set

Familial Glucocorticoid Deficiency 1 Gene Set

Glucocorticoid deficiency 2 Gene Set

Glucocorticoid deficiency 4 Gene Set

Glucocorticoid deficiency with achalasia Gene Set

Glucocorticoid Deficiency 2 Gene Set

Glucocorticoid Deficiency 3 Gene Set

NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT Gene Set

glucocorticoid deficiency Gene Set

glucocorticoid deficiency, due to acth unresponsiveness Gene Set

natural killer cell and glucocorticoid deficiency with dna repair defect Gene Set

glucocorticoid deficiency 2 Gene Set

glucocorticoid deficiency 3 Gene Set

glucocorticoid deficiency 4 Gene Set

Glucocorticoid Deficiency With Achalasia Gene Set

Glucocorticoid Receptor Deficiency Gene Set

Glucocorticoid Deficiency Gene Set

Glucocorticoid deficiency 1 Gene Set

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

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

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

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

amyloidosis, familial; familial mediterranean fever Gene Set

albuminuria; amyloidosis, familial; familial mediterranean fever Gene Set

multiple familial trichoepithelioma and familial cylindromatosis Gene Set

amyloidosis, familial; familial mediterranean fever; Gene Set

familial hemiplegic migraine and benign familial infantile convulsions Gene Set

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

Glucocorticoid resistance, generalized Gene Set

Glucocorticoid-Remediable Aldosteronism Gene Set

glucocorticoid-remediable aldosteronism Gene Set

bcli restriction fragment length polymorphism at the glucocorticoid receptor gene locus Gene Set

glucocorticoid sensitivity Gene Set

glucocorticoid Gene Set

positive regulation of glucocorticoid biosynthetic process Gene Set

regulation of glucocorticoid receptor signaling pathway Gene Set

cellular response to glucocorticoid stimulus Gene Set

regulation of glucocorticoid mediated signaling pathway Gene Set

negative regulation of glucocorticoid secretion Gene Set

glucocorticoid receptor signaling pathway Gene Set

response to glucocorticoid Gene Set

glucocorticoid mediated signaling pathway Gene Set

positive regulation of glucocorticoid metabolic process Gene Set

glucocorticoid biosynthetic process Gene Set

glucocorticoid metabolic process Gene Set

regulation of glucocorticoid metabolic process Gene Set

negative regulation of glucocorticoid metabolic process Gene Set

glucocorticoid secretion Gene Set

glucocorticoid catabolic process Gene Set

positive regulation of glucocorticoid secretion Gene Set

negative regulation of glucocorticoid receptor signaling pathway Gene Set

negative regulation of glucocorticoid biosynthetic process Gene Set

regulation of glucocorticoid secretion Gene Set

negative regulation of glucocorticoid mediated signaling pathway Gene Set

positive regulation of glucocorticoid receptor signaling pathway Gene Set

regulation of glucocorticoid biosynthetic process Gene Set

glucocorticoid receptor activity Gene Set

glucocorticoid-activated rna polymerase ii transcription factor binding transcription factor activity Gene Set

glucocorticoid receptor binding Gene Set

abnormality of circulating glucocorticoid level Gene Set

abnormality of circulating glucocorticoid level Gene Set

Glucocorticoid receptor Gene Set

Glucocorticoid-induced transcript 1 protein Gene Set

Glucocorticoid-induced transcript 1/FAM117 Gene Set

Glucocorticoid modulatory element-binding protein 1/2 Gene Set

decreased circulating glucocorticoid level Gene Set

increased circulating glucocorticoid level Gene Set

abnormal circulating glucocorticoid level Gene Set

glucocorticoid resistance Gene Set

aldosteronism, glucocorticoid-remediable Gene Set

{glucocorticoid therapy, response to} Gene Set

glucocorticoid Gene Set

Rapid glucocorticoid signaling Gene Set

Glucocorticoid receptor regulatory network Gene Set

Glucocorticoid biosynthesis Gene Set

Glucocorticoid & Mineralcorticoid Metabolism(Mus musculus) Gene Set