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amyloidosis; familial mediterranean fever Gene SetFrom 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. |
abdominal pain; amyloidosis; arthritis; familial mediterranean fever; fever Gene SetFrom 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. |
amyloidosis, familial; familial mediterranean fever Gene SetFrom 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 SetFrom 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. |
amyloidosis, familial; familial mediterranean fever; Gene SetFrom 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. |
amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome Gene SetFrom 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. |
amyloidosis; familial mediterranean fever; tuberculosis, pulmonary Gene SetFrom 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. |
amyloidosis; familial mediterranean fever; inflammation Gene SetFrom 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. |
amyloidosis; arthritis, rheumatoid; familial mediterranean fever; Gene SetFrom 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; atherosclerosis; familial mediterranean fever; Gene SetFrom 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. |
amyloidosis; arthritis, rheumatoid; familial mediterranean fever Gene SetFrom 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 mediterranean fever; fever Gene SetFrom 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 Mediterranean fever Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial Mediterranean fever phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial Mediterranean Fever, Autosomal Dominant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial Mediterranean Fever, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset. |
Familial Mediterranean Fever Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial Mediterranean Fever from the curated CTD Gene-Disease Associations dataset. |
familial mediterranean fever Gene SetFrom 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 mediterranean fever Gene SetFrom 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. |
arthritis, rheumatoid; familial mediterranean fever; rheumatoid arthritis; rheumatoid spondylitis; spondylitis, ankylosing Gene SetFrom 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 SetFrom 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. |
familial mediterranean fever; spondylitis, ankylosing Gene SetFrom 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. |
asthma; familial mediterranean fever Gene SetFrom 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 mediterranean fever; henoch-schoenlein purpura; purpura, schoenlein-henoch Gene SetFrom 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. |
familial mediterranean fever; glomerulonephritis, iga; iga glomerulonephritides Gene SetFrom 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. |
arthritis, juvenile rheumatoid; arthritis, psoriatic; familial mediterranean fever; Gene SetFrom 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 SetFrom 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. |
familial mediterranean fever; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid; leukemia, myeloid, acute; myelodysplastic syndromes; myeloid leukemia; polycythemia vera; preleukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid; leukemia, myeloid, acute; myelodysplastic syndromes; myeloid leukemia; polycythemia vera; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial mediterranean fever Gene SetFrom 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. |
cystic fibrosis; familial mediterranean fever Gene SetFrom 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. |
colitis, ulcerative; crohn disease; familial mediterranean fever; inflammatory bowel diseases Gene SetFrom 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. |
body weight; familial mediterranean fever; recurrence Gene SetFrom 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. |
cryopyrin-associated periodic syndromes; familial mediterranean fever; mevalonate kinase deficiency Gene SetFrom 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. |
arthritis, juvenile rheumatoid; familial mediterranean fever; Gene SetFrom 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. |
familial mediterranean fever; Gene SetFrom 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. |
arthritis; familial mediterranean fever Gene SetFrom 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 mediterranean fever; infertility, male Gene SetFrom 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. |
diarrhea; familial mediterranean fever; pain; stomatitis, aphthous Gene SetFrom 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. |
creutzfeldt-jakob disease; creutzfeldt-jakob syndrome; familial mediterranean fever Gene SetFrom 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. |
arthritis, juvenile rheumatoid; chronic childhood arthritis; familial mediterranean fever; inflammation Gene SetFrom 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 mediterranean fever; hyper-igd syndrome Gene SetFrom 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 Gene SetFrom 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. |
familial mediterranean fever, ar Gene SetFrom OMIM Gene-Disease Associations genes associated with the familial mediterranean fever, ar phenotype from the curated OMIM Gene-Disease Associations dataset. |
familial mediterranean fever, ad Gene SetFrom OMIM Gene-Disease Associations genes associated with the familial mediterranean fever, ad phenotype from the curated OMIM Gene-Disease Associations dataset. |
Familial Mediterranean Fever Gene SetFrom 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 Mediterranean Fever, Autosomal Dominant Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Mediterranean Fever, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Mediterranean fever Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Familial Mediterranean fever from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Familial Mediterranean fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial Mediterranean fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial Mediterranean fever Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial Mediterranean fever phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
mediterranean fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dengue; dengue fever; dengue hemorrhagic fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dengue; dengue fever; dengue hemorrhagic fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
paratyphoid fever; typhoid fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease paratyphoid fever; typhoid fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Familial visceral amyloidosis, Ostertag type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial visceral amyloidosis, Ostertag type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Amyloidosis, familial visceral Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Amyloidosis, familial visceral from the curated CTD Gene-Disease Associations dataset. |
Amyloidosis, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Amyloidosis, Familial from the curated CTD Gene-Disease Associations dataset. |
familial visceral amyloidosis Gene SetFrom 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. |
amyloidosis, familial; cerebral hemorrhage; cerebral hemorrhages Gene SetFrom 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. |
Amyloidosis, Familial Gene SetFrom 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. |
amyloidosis, familial visceral Gene SetFrom OMIM Gene-Disease Associations genes associated with the amyloidosis, familial visceral phenotype from the curated OMIM Gene-Disease Associations dataset. |
Familial Lichen Amyloidosis Gene SetFrom 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. |
Familial Non-Neuropathic Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Non-Neuropathic Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial visceral amyloidosis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Familial visceral amyloidosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Familial visceral amyloidosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial visceral amyloidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial visceral amyloidosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial visceral amyloidosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Periodic fever, familial, autosomal dominant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Periodic fever, familial, autosomal dominant from the curated CTD Gene-Disease Associations dataset. |
periodic fever, familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the periodic fever, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
Autosomal dominant familial periodic fever Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant familial periodic fever from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Autosomal dominant familial periodic fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant familial periodic fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial Periodic Fever Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial Periodic Fever phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
mediterranean visceral leishmaniasis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease mediterranean visceral leishmaniasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
mediterranean Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term mediterranean in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Macrothrombocytopenia-Stomatocytosis, Mediterranean Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Macrothrombocytopenia-Stomatocytosis, Mediterranean in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Serum polyunsaturated fatty acid concentration x Mediterranean diet adherence interaction in metabolic syndrome Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Serum polyunsaturated fatty acid concentration x Mediterranean diet adherence interaction in metabolic syndrome phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Adiponectin levels x Mediterranean diet adherence interaction Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Adiponectin levels x Mediterranean diet adherence interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Serum bilirubin levels x Mediterranean diet adherence interaction in metabolic syndrome Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Serum bilirubin levels x Mediterranean diet adherence interaction in metabolic syndrome phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN from the curated CTD Gene-Disease Associations dataset. |
multiple familial trichoepithelioma and familial cylindromatosis Gene SetFrom 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. |
familial hemiplegic migraine and benign familial infantile convulsions Gene SetFrom 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. |
Cutaneous amyloidosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cutaneous amyloidosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Amyloidogenic transthyretin amyloidosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Amyloidogenic transthyretin amyloidosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
AMYLOIDOSIS, LEPTOMENINGEAL, TRANSTHYRETIN-RELATED Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the AMYLOIDOSIS, LEPTOMENINGEAL, TRANSTHYRETIN-RELATED phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebral hemorrhage with amyloidosis, hereditary, Dutch type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral hemorrhage with amyloidosis, hereditary, Dutch type from the curated CTD Gene-Disease Associations dataset. |
Amyloidosis, Hereditary, Transthyretin-Related Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Amyloidosis, Hereditary, Transthyretin-Related from the curated CTD Gene-Disease Associations dataset. |
Amyloidosis IX Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Amyloidosis IX from the curated CTD Gene-Disease Associations dataset. |
Amyloidosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Amyloidosis from the curated CTD Gene-Disease Associations dataset. |
transthyretin amyloidosis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease transthyretin amyloidosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
finnish type amyloidosis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease finnish type amyloidosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
amyloidosis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease amyloidosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
amyloidosis Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease amyloidosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
transthyretin amyloidosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease transthyretin amyloidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
primary cutaneous amyloidosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary cutaneous amyloidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
amyloidosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease amyloidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
renal amyloidosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease renal amyloidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amyloidosis; arthritis, rheumatoid; liver diseases; rheumatoid arthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amyloidosis; arthritis, rheumatoid; liver diseases; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
massive leptomeningeal amyloidosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease massive leptomeningeal amyloidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amyloidosis; anemia; chronic disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amyloidosis; anemia; chronic disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiac and cutaneous amyloidosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiac and cutaneous amyloidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cutaneous lichen amyloidosis. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cutaneous lichen amyloidosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amyloidosis; heart diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amyloidosis; heart diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amyloidosis; arthritis, rheumatoid; rheumatoid arthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amyloidosis; arthritis, rheumatoid; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
secondary and fmf amyloidosis. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease secondary and fmf amyloidosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
early-onset aggressive diffuse amyloidosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease early-onset aggressive diffuse amyloidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; amyloidosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; amyloidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amyloidosis; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amyloidosis; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
vitreous amyloidosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease vitreous amyloidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amyloidosis; kidney diseases; postoperative complications; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amyloidosis; kidney diseases; postoperative complications; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amyloidosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amyloidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amyloidosis Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term amyloidosis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
amyloidosis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the amyloidosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
renal amyloidosis Gene SetFrom HPO Gene-Disease Associations genes associated with the renal amyloidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hepatic amyloidosis Gene SetFrom HPO Gene-Disease Associations genes associated with the hepatic amyloidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cutaneous amyloidosis Gene SetFrom HPO Gene-Disease Associations genes associated with the cutaneous amyloidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
amyloidosis Gene SetFrom HPO Gene-Disease Associations genes associated with the amyloidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Amyloidosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Amyloidosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
amyloidosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the amyloidosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
amyloidosis, renal Gene SetFrom OMIM Gene-Disease Associations genes associated with the amyloidosis, renal phenotype from the curated OMIM Gene-Disease Associations dataset. |
amyloidosis, 3 or more types Gene SetFrom OMIM Gene-Disease Associations genes associated with the amyloidosis, 3 or more types phenotype from the curated OMIM Gene-Disease Associations dataset. |
amyloidosis, primary localized cutaneous, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the amyloidosis, primary localized cutaneous, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
amyloidosis, primary localized cutaneous, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the amyloidosis, primary localized cutaneous, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
amyloidosis, finnish type Gene SetFrom OMIM Gene-Disease Associations genes associated with the amyloidosis, finnish type phenotype from the curated OMIM Gene-Disease Associations dataset. |
{?amyloidosis, secondary, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {?amyloidosis, secondary, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
amyloidosis, hereditary, transthyretin-related Gene SetFrom OMIM Gene-Disease Associations genes associated with the amyloidosis, hereditary, transthyretin-related phenotype from the curated OMIM Gene-Disease Associations dataset. |
Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Systemic Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Systemic Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Systemic Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Systemic Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Age-Related Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Age-Related Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Senile Systemic Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Senile Systemic Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aa Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aa Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Reactive Systemic Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Reactive Systemic Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Localized Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Localized Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatic Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Cardiac Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Cardiac Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Systemic Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Systemic Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Laryngeal Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Laryngeal Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Nodular Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Nodular Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Senile Cardiac Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Senile Cardiac Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cerebral Hemorrhage With Amyloidosis, Hereditary, Dutch Type Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Hemorrhage With Amyloidosis, Hereditary, Dutch Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cerebrovascular Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cerebrovascular Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Cerebrovascular Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Cerebrovascular Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Autosomal Dominant Beta2-Microglobulinic Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Beta2-Microglobulinic Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hemodialysis-Associated Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hemodialysis-Associated Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Light Chain (Al) Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Light Chain (Al) Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Transthyretin Cardiac Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Transthyretin Cardiac Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Senile Systemic Amyloidosis (Ssa) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Senile Systemic Amyloidosis (Ssa) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Inherited Systemic Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Inherited Systemic Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Gastrointestinal Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Gastrointestinal Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Macular Cutaneous Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Macular Cutaneous Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Macular Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Macular Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Nodular Cutaneous Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Nodular Cutaneous Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pulmonary Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cutaneous Lichen Amyloidosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cutaneous Lichen Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
amyloidosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the amyloidosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Amyloidosis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Amyloidosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Primary cutaneous amyloidosis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Primary cutaneous amyloidosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Finnish type amyloidosis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Finnish type amyloidosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Transthyretin amyloidosis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Transthyretin amyloidosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Amyloidosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Amyloidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Transthyretin amyloidosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Transthyretin amyloidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Serum amyloid A amyloidosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Serum amyloid A amyloidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Immunoglobulin light chain amyloidosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Immunoglobulin light chain amyloidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Finnish type amyloidosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Finnish type amyloidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary cutaneous amyloidosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary cutaneous amyloidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
wild-type amyloidosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease wild-type amyloidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary localized cutaneous amyloidosis 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary localized cutaneous amyloidosis 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Immunoglobulin heavy chain amyloidosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Immunoglobulin heavy chain amyloidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
dialysis-related amyloidosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease dialysis-related amyloidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Apolipoprotein A-IV associated amyloidosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Apolipoprotein A-IV associated amyloidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Amyloidosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Amyloidosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
ATTRV122I amyloidosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the ATTRV122I amyloidosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hereditary amyloidosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary amyloidosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
ABeta amyloidosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the ABeta amyloidosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
AFib amyloidosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the AFib amyloidosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
ADan amyloidosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the ADan amyloidosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
ABri amyloidosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the ABri amyloidosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Immunoglobulin light chain (AL) amyloidosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Immunoglobulin light chain (AL) amyloidosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Immunoglobulin light chain (AL) amyloidosis (liver involvement) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Immunoglobulin light chain (AL) amyloidosis (liver involvement) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Immunoglobulin light chain (AL) amyloidosis (serum Ig lambda profile) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Immunoglobulin light chain (AL) amyloidosis (serum Ig lambda profile) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Immunoglobulin light chain (AL) amyloidosis (serum IgG profile) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Immunoglobulin light chain (AL) amyloidosis (serum IgG profile) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
TNF receptor-associated periodic fever syndrome (TRAPS) Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the TNF receptor-associated periodic fever syndrome (TRAPS) phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperimmunoglobulin D with periodic fever Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperimmunoglobulin D with periodic fever phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Periodic fever, menstrual cycle-dependent Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Periodic fever, menstrual cycle-dependent phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
West Nile Fever Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease West Nile Fever from the curated CTD Gene-Disease Associations dataset. |
Lassa Fever Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lassa Fever from the curated CTD Gene-Disease Associations dataset. |
Typhoid Fever Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Typhoid Fever from the curated CTD Gene-Disease Associations dataset. |
Fever Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Fever from the curated CTD Gene-Disease Associations dataset. |
Dengue Hemorrhagic Fever Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Dengue Hemorrhagic Fever in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
flinders island spotted fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease flinders island spotted fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
typhoid fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease typhoid fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
relapsing fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease relapsing fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
uveoparotid fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease uveoparotid fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pharyngoconjunctival fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pharyngoconjunctival fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
spotted fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spotted fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
venezuelan hemorrhagic fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease venezuelan hemorrhagic fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bolivian hemorrhagic fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bolivian hemorrhagic fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
phlebotomus fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease phlebotomus fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
trench fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease trench fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
ebola hemorrhagic fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ebola hemorrhagic fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
blackwater fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease blackwater fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
colorado tick fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease colorado tick fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
louse-borne relapsing fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease louse-borne relapsing fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
yellow fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease yellow fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
tick-borne relapsing fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease tick-borne relapsing fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
west nile fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease west nile fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
crimean-congo hemorrhagic fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease crimean-congo hemorrhagic fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
african tick-bite fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease african tick-bite fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
far eastern spotted fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease far eastern spotted fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
sennetsu fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sennetsu fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
paratyphoid fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease paratyphoid fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
japanese spotted fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease japanese spotted fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
argentine hemorrhagic fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease argentine hemorrhagic fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
q fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease q fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
rift valley fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease rift valley fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pontiac fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pontiac fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
boutonneuse fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease boutonneuse fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
scarlet fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease scarlet fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
rheumatic fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease rheumatic fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
marburg hemorrhagic fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease marburg hemorrhagic fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lassa fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lassa fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
dengue hemorrhagic fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dengue hemorrhagic fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
rocky mountain spotted fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease rocky mountain spotted fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
korean hemorrhagic fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease korean hemorrhagic fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
ross river fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ross river fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hemorrhagic fever with renal syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hemorrhagic fever with renal syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
dengue hemorrhagic fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dengue hemorrhagic fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
disease models, animal; fever; seizures, febrile Gene SetFrom GAD Gene-Disease Associations genes associated with the disease disease models, animal; fever; seizures, febrile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dengue; dengue hemorrhagic fever; thrombocytopenia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dengue; dengue hemorrhagic fever; thrombocytopenia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
boutonneuse fever; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease boutonneuse fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
rheumatic fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease rheumatic fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hemorrhagic fever, crimean Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hemorrhagic fever, crimean in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leptospirosis; swamp fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leptospirosis; swamp fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hay fever; nasal obstruction; rhinitis, allergic, perennial; rhinitis, allergic, seasonal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hay fever; nasal obstruction; rhinitis, allergic, perennial; rhinitis, allergic, seasonal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; asthma; emphysema; bronchitis; pneumonia; hay fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; asthma; emphysema; bronchitis; pneumonia; hay fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hemorrhagic fever with renal syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hemorrhagic fever with renal syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
rheumatic fever; rheumatic heart disease; streptococcal infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease rheumatic fever; rheumatic heart disease; streptococcal infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
q fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease q fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
asthma; eczema; hay fever; hypersensitivity; respiratory sounds; rhinitis, allergic, perennial; rhinitis, allergic, seasonal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease asthma; eczema; hay fever; hypersensitivity; respiratory sounds; rhinitis, allergic, perennial; rhinitis, allergic, seasonal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
asthma; brain neoplasms; eczema; glioma; hay fever; hypersensitivity; rhinitis, allergic, seasonal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease asthma; brain neoplasms; eczema; glioma; hay fever; hypersensitivity; rhinitis, allergic, seasonal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hay fever; rhinitis, allergic, seasonal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hay fever; rhinitis, allergic, seasonal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dengue; dengue fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dengue; dengue fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dengue hemorrhagic fever; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dengue hemorrhagic fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fever; hemolysis; inflammation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fever; hemolysis; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hemorrhagic fever, ebola Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hemorrhagic fever, ebola in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hemorrhagic fever with renal syndrome; pleural effusion Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hemorrhagic fever with renal syndrome; pleural effusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myocarditis; rheumatic fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocarditis; rheumatic fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
west nile fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease west nile fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
boutonneuse fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease boutonneuse fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
rheumatic fever; rheumatic heart disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease rheumatic fever; rheumatic heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; fever; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
typhoid fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease typhoid fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hay fever; rhinitis, allergic, perennial; rhinitis, allergic, seasonal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hay fever; rhinitis, allergic, perennial; rhinitis, allergic, seasonal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alphavirus infections; infectious mononucleosis; q fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alphavirus infections; infectious mononucleosis; q fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fever; neoplasms; neutropenia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fever; neoplasms; neutropenia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
asthma; hay fever; rhinitis, allergic, perennial; rhinitis, allergic, seasonal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease asthma; hay fever; rhinitis, allergic, perennial; rhinitis, allergic, seasonal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fever Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term fever in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Lassa Fever Virus_24hr_24069471_GSE41300 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Viral Infections genes differentially expressed following the Lassa Fever Virus_24hr_24069471_GSE41300 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset. |
Lassa Fever Virus_8hr_24069471_GSE41300 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Viral Infections genes differentially expressed following the Lassa Fever Virus_8hr_24069471_GSE41300 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset. |
Lassa Fever Virus_4hr_24069471_GSE41300 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Viral Infections genes differentially expressed following the Lassa Fever Virus_4hr_24069471_GSE41300 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset. |
positive regulation of fever generation by positive regulation of prostaglandin secretion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of fever generation by positive regulation of prostaglandin secretion biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of fever generation by regulation of prostaglandin secretion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of fever generation by regulation of prostaglandin secretion biological process from the curated GO Biological Process Annotations 2015 dataset. |
fever generation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the fever generation biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of fever generation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of fever generation biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of fever generation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of fever generation biological process from the curated GO Biological Process Annotations 2015 dataset. |
Asthma and hay fever Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Asthma and hay fever phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
fever Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the fever phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
fever Gene SetFrom HPO Gene-Disease Associations genes associated with the fever phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
episodic fever Gene SetFrom HPO Gene-Disease Associations genes associated with the episodic fever phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
West Nile Fever Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the West Nile Fever phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Fever of Unknown Origin Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Fever of Unknown Origin phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Paratyphoid Fever Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Paratyphoid Fever phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Dengue Hemorrhagic Fever Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Dengue Hemorrhagic Fever phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hemorrhagic Fever, Ebola Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hemorrhagic Fever, Ebola phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hemorrhagic Fever, Crimean Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hemorrhagic Fever, Crimean phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hemorrhagic Fever with Renal Syndrome Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hemorrhagic Fever with Renal Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Typhoid Fever Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Typhoid Fever phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Uveoparotid Fever Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Uveoparotid Fever phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Yellow Fever Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Yellow Fever phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Rheumatic Fever Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Rheumatic Fever phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Fever Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Fever phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Boutonneuse Fever Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Boutonneuse Fever phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Q Fever Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Q Fever phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
periodic fever, menstrual cycle dependent Gene SetFrom OMIM Gene-Disease Associations genes associated with the periodic fever, menstrual cycle dependent phenotype from the curated OMIM Gene-Disease Associations dataset. |
{dengue fever, protection against} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {dengue fever, protection against} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{plasmodium falciparum fever episodes qtl1} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {plasmodium falciparum fever episodes qtl1} phenotype from the curated OMIM Gene-Disease Associations dataset. |
African swine fever virus Gene SetFrom Virus MINT Protein-Virus Interactions interacting proteins for the virus African swine fever virus from the Virus MINT Protein-Virus Interactions dataset. |
Hay Fever Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hay Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Paratyphoid Fever Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Paratyphoid Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Rheumatic Fever Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Rheumatic Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dengue Fever Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dengue Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Typhoid Fever Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Typhoid Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
West Nile Fever Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease West Nile Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Tick Fever Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Tick Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Q Fever Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Q Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Rift Valley Fever Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Rift Valley Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Relapsing Fever Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Relapsing Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Tnf Receptor-Associated Periodic Fever Syndrome (Traps) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Tnf Receptor-Associated Periodic Fever Syndrome (Traps) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chikungunya Fever Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chikungunya Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Periodic Fever Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Periodic Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Tick-Borne Fever Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Tick-Borne Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Yellow Fever Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Yellow Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Disorder Characterized By Fever Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Disorder Characterized By Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chronic Q Fever Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chronic Q Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lassa Fever Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lassa Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Boutonneuse Fever Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Boutonneuse Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Fever With Thrombocytopenia Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Fever With Thrombocytopenia Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Periodic Fever Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Periodic Fever Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Periodic Fever, Aphthous Stomatitis, Pharyngitis, Adenitis Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Periodic Fever, Aphthous Stomatitis, Pharyngitis, Adenitis Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Yellow Fever Vaccine-Associated Viscerotropic Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Yellow Fever Vaccine-Associated Viscerotropic Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Encephalitis, West Nile Fever Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Encephalitis, West Nile Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
East Coast Fever Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease East Coast Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Tick-Borne Relapsing Fever Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Tick-Borne Relapsing Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acute Q Fever Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acute Q Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Spotted Fever Group Rickettsiosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Spotted Fever Group Rickettsiosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Rocky Mountain Spotted Fever Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Rocky Mountain Spotted Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Scarlet Fever Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Scarlet Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Uveoparotid Fever Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Uveoparotid Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Oroya Fever Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Oroya Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pontiac Fever Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pontiac Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Q Fever Endocarditis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Q Fever Endocarditis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Brazilian Purpuric Fever Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Brazilian Purpuric Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Periodic Fever, Aphthous Stomatitis, Pharyngitis, And Adenopathy Syndrome [Pfapa] Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Periodic Fever, Aphthous Stomatitis, Pharyngitis, And Adenopathy Syndrome [Pfapa] in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hyper-Igd Periodic Fever Syndrome (Hids) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hyper-Igd Periodic Fever Syndrome (Hids) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
African Swine Fever Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease African Swine Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Rheumatic Fever In Children Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Rheumatic Fever In Children in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fever Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low Grade Fever Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low Grade Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cough With Fever Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cough With Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fever With Chills Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fever With Chills in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Intrapartum Fever Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intrapartum Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Maternal Fever In Pregnancy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Maternal Fever In Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Maternal First Trimester Fever Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Maternal First Trimester Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Maternal Fever Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Maternal Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Intermittent Fever Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intermittent Fever in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fever With Rash Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fever With Rash in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
regulation of fever generation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of fever generation biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of fever generation by positive regulation of prostaglandin secretion Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of fever generation by positive regulation of prostaglandin secretion biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of fever generation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of fever generation biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of fever generation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of fever generation biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of fever generation by positive regulation of prostaglandin secretion Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of fever generation by positive regulation of prostaglandin secretion biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of fever generation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of fever generation biological process from the curated GO Biological Process Annotations 2025 dataset. |
Dengue hemorrhagic fever Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Dengue hemorrhagic fever in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Typhoid fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Typhoid fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Ebola hemorrhagic fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ebola hemorrhagic fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Paratyphoid fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Paratyphoid fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Omsk hemorrhagic fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Omsk hemorrhagic fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Relapsing fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Relapsing fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Rocky Mountain spotted fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Rocky Mountain spotted fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Q fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Q fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
tick-borne relapsing fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease tick-borne relapsing fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Spotted fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spotted fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Crimean-Congo hemorrhagic fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Crimean-Congo hemorrhagic fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Oropouche fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Oropouche fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Rift Valley fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Rift Valley fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
louse-borne relapsing fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease louse-borne relapsing fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lassa fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lassa fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
African tick-bite fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease African tick-bite fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Boutonneuse fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Boutonneuse fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Yellow fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Yellow fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Dengue hemorrhagic fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dengue hemorrhagic fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hantavirus hemorrhagic fever with renal syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hantavirus hemorrhagic fever with renal syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Trench fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Trench fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Zika fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Zika fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
West Nile fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease West Nile fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Rheumatic fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Rheumatic fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Alkhurma hemorrhagic fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Alkhurma hemorrhagic fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
O'nyong'nyong fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease O'nyong'nyong fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Scarlet fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Scarlet fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Uveoparotid fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Uveoparotid fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Marburg hemorrhagic fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Marburg hemorrhagic fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hyperimmunoglobulinemia D periodic fever syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hyperimmunoglobulinemia D periodic fever syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Argentine hemorrhagic fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Argentine hemorrhagic fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Ross River fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ross River fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Bolivian hemorrhagic fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bolivian hemorrhagic fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Colorado tick fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Colorado tick fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Brazilian hemorrhagic fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Brazilian hemorrhagic fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Korean hemorrhagic fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Korean hemorrhagic fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Pharyngoconjunctival fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pharyngoconjunctival fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Venezuelan hemorrhagic fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Venezuelan hemorrhagic fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Pontiac fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pontiac fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Phlebotomus fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Phlebotomus fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Sennetsu fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sennetsu fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aneruptive fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aneruptive fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Far Eastern spotted fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Far Eastern spotted fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Blackwater fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Blackwater fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lujo hemorrhagic fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lujo hemorrhagic fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Chapare hemorrhagic fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chapare hemorrhagic fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Flinders Island spotted fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Flinders Island spotted fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Haverhill fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Haverhill fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Japanese spotted fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Japanese spotted fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Astrakhan spotted fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Astrakhan spotted fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Recurrent fever Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Recurrent fever phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
TNF receptor-associated periodic fever syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the TNF receptor-associated periodic fever syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Periodic fever-infantile enterocolitis-autoinflammatory syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Periodic fever-infantile enterocolitis-autoinflammatory syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Periodic fever syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Periodic fever syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Allergic disease (asthma, hay fever and/or eczema) (age of onset) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Allergic disease (asthma, hay fever and/or eczema) (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Allergic disease (asthma, hay fever and/or eczema) (multivariate analysis) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Allergic disease (asthma, hay fever and/or eczema) (multivariate analysis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Allergic disease (asthma, hay fever or eczema) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Allergic disease (asthma, hay fever or eczema) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Scarlet fever Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Scarlet fever phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Menstruation quality of life impact (fever) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Menstruation quality of life impact (fever) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Fever and diarrhea in mesalamine-treated irritable bowel disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Fever and diarrhea in mesalamine-treated irritable bowel disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Enteric fever Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Enteric fever phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Asthma and hay fever Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma and hay fever phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Thrombocytosis, benign familial microcytic Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Erythrocytosis, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Erythrocytosis, familial, 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Erythrocytosis, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Erythrocytosis, familial, 2 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperpigmentation, familial progressive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial aortopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial aortopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Digital arthropathy-brachydactyly, familial Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dementia familial British Gene SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial porencephaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hypertrophic cardiomyopathy 17 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the familial hyperinsulinism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperinsulinemic hypoglycemia familial 3 Gene SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Paroxysmal familial ventricular fibrillation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hypercholesterolemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial hypercholesterolemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hidradenitis suppurativa, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hidradenitis suppurativa, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dementia, familial Danish Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial dysautonomia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial febrile seizures 8 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myoclonus, familial cortical phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Migraine, familial basilar Gene SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypercholanemia, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bone marrow failure, familial Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Candidiasis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Candidiasis, familial, 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Candidiasis, familial, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hypokalemia-hypomagnesemia Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Tumoral calcinosis, familial, normophosphatemic phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cd8 deficiency, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cd8 deficiency, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial infantile myasthenia Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial pulmonary capillary hemangiomatosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hypoalphalipoproteinemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial hypoalphalipoproteinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial renal hypouricemia Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial myelofibrosis from the curated CTD Gene-Disease Associations dataset. |
Nephronophthisis, familial juvenile Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Nephronophthisis, familial juvenile from the curated CTD Gene-Disease Associations dataset. |
Eosinophilia, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Eosinophilia, Familial from the curated CTD Gene-Disease Associations dataset. |
Hyperlipidemia, Familial Combined Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 6 from the curated CTD Gene-Disease Associations dataset. |
Cardiomyopathy, Hypertrophic, Familial Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Gliosis, Familial Progressive Subcortical from the curated CTD Gene-Disease Associations dataset. |
CD8 Deficiency, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease CD8 Deficiency, Familial from the curated CTD Gene-Disease Associations dataset. |
Insomnia, Fatal Familial Gene SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL NEONATAL, 2 from the curated CTD Gene-Disease Associations dataset. |
Familial HDL deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial HDL deficiency from the curated CTD Gene-Disease Associations dataset. |
Familial dermographism Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial dermographism from the curated CTD Gene-Disease Associations dataset. |
Candidiasis, Familial, 3 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pseudohyperkalemia, Familial, 2, due to Red Cell Leak from the curated CTD Gene-Disease Associations dataset. |
Cirrhosis, Familial Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 3 from the curated CTD Gene-Disease Associations dataset. |
Familial Hypophosphatemic Rickets Gene SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Keratoacanthoma familial from the curated CTD Gene-Disease Associations dataset. |
Hepatic Adenomas, Familial Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial antiphospholipid syndrome from the curated CTD Gene-Disease Associations dataset. |
Familial paroxysmal dystonia Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Atrial myxoma, familial from the curated CTD Gene-Disease Associations dataset. |
Familial Glucocorticoid Deficiency 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial Glucocorticoid Deficiency 1 from the curated CTD Gene-Disease Associations dataset. |
Tumoral Calcinosis, Normophosphatemic, Familial Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hemophagocytic lymphohistiocytosis, familial, 2 from the curated CTD Gene-Disease Associations dataset. |
VENTRICULAR TACHYCARDIA, FAMILIAL Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hemiplegic migraine, familial type 1 from the curated CTD Gene-Disease Associations dataset. |
Familial apoceruloplasmin deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial apoceruloplasmin deficiency from the curated CTD Gene-Disease Associations dataset. |
HYPERCHOLESTEROLEMIA, FAMILIAL Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HYPERCHOLESTEROLEMIA, FAMILIAL from the curated CTD Gene-Disease Associations dataset. |
Amyloid Neuropathies, Familial Gene SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease CANDIDIASIS, FAMILIAL, 2 from the curated CTD Gene-Disease Associations dataset. |
Febrile Convulsions, Familial, 7 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 14 from the curated CTD Gene-Disease Associations dataset. |
familial adenomatous polyposis Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 lipoprotein lipase deficiency Gene SetFrom 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 periodic paralysis Gene SetFrom 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 lipoprotein lipase deficiency Gene SetFrom 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. |
familial hypertriglyceridemia Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 nephrotic syndrome Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 atrial fibrillation Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
hyperlipidemia, familial combined Gene SetFrom 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. |
mild familial hypercholesterolemia Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
familial hypercholesterolemia Gene SetFrom 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 SetFrom 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. |
familial hypercholesterolaemia Gene SetFrom 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. |
coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases Gene SetFrom 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. |
amyloid neuropathies; amyloid neuropathies, familial Gene SetFrom 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 SetFrom 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 SetFrom 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. |
coronary artery disease; hyperlipidemia, familial combined Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 type 3 hyperlipoproteinaemia; hyperlipoproteinemia type iii Gene SetFrom 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 SetFrom 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 SetFrom 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. |
late onset of familial adenomatous polyposis Gene SetFrom 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 SetFrom 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 SetFrom 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. |
hyperlipidemia, familial combined; mixed hyperlipidemia Gene SetFrom 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. |
familial defective apolipoprotein b-100 in a chinese man Gene SetFrom 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. |
premature coronary artery disease and familial hypoalphalipoproteinemia Gene SetFrom 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. |
familial male-limited precocious puberty. Gene SetFrom 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 SetFrom 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. |
fam hyperbetalipoproteinaemia; hyperlipidemia, familial combined; hyperlipoproteinemia type ii; hypertriglyceridemia; mixed hyperlipidemia Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
cardiovascular diseases; coronary artery disease; hyperlipidemia, familial combined; mixed hyperlipidemia Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 glucocorticoid deficiency Gene SetFrom 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. |
late onset familial adenomatous polyposis Gene SetFrom 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. |
familial amyloid polyneuropathy Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 liver adenomatosis Gene SetFrom 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. |
breast cancer, familial Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
coronary artery disease; hyperlipidemia, familial combined; metabolic syndrome x; mixed hyperlipidemia Gene SetFrom 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. |
blood pressure; hyperlipidemia, familial combined Gene SetFrom 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. |
creutzfeldt-jakob disease; gerstmann-straussler-scheinker disease; insomnia, fatal familial Gene SetFrom 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 SetFrom 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 SetFrom 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. |
familial dysautonomia Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
familial non-ret c cell hyperplasia Gene SetFrom 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 SetFrom 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 SetFrom 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 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Lipodystrophy, Familial Partial Gene SetFrom 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. |
Dysautonomia, Familial Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the insomnia, fatal familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
dysautonomia, familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the dysautonomia, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
febrile seizures, familial, 9 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
[igg receptor i, phagocytic, familial deficiency of] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [igg receptor i, phagocytic, familial deficiency of] phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyperuricemic nephropathy, familial juvenile 1 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the hemophagocytic lymphohistiocytosis, familial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
migraine, familial hemiplegic, 1, with progressive cerebellar ataxia Gene SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the hematuria, familial benign phenotype from the curated OMIM Gene-Disease Associations dataset. |
hematuria, benign familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the hematuria, benign familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
dementia, familial british Gene SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the pseudohyperkalemia, familial, 2, due to red cell leak phenotype from the curated OMIM Gene-Disease Associations dataset. |
myasthenia, limb-girdle, familial Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the thrombophilia, familial, due to decreased release of plat phenotype from the curated OMIM Gene-Disease Associations dataset. |
cylindromatosis, familial Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the {hypercholesterolemia, familial, due to ldlr defect, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset. |
advanced sleep phase syndrome, familial, 1 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the erythrocytosis, familial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
erythrocytosis, familial, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the erythrocytosis, familial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
erythrocytosis, familial, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the erythrocytosis, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
hypercholesterolemia, familial, 3 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the episodic pain syndrome, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
epilepsy, familial adult myoclonic, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the epilepsy, familial adult myoclonic, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cd8 deficiency, familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the cd8 deficiency, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
gastric cancer, familial diffuse, with or without cleft lip and/or palate Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the myoclonic epilepsy, infantile, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
hypercholesterolemia, familial Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the arrhythmogenic right ventricular dysplasia, familial, 13 phenotype from the curated OMIM Gene-Disease Associations dataset. |
ventricular fibrillation, familial, 1 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the goiter, familial, due to ttf-1 defect phenotype from the curated OMIM Gene-Disease Associations dataset. |