| Name |
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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. |
lung cancer; breast cancer; liver cancer; oral cancer; prostate cancer; thyroid cancer; cervical cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; breast cancer; liver cancer; oral cancer; prostate cancer; thyroid cancer; cervical cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; breast cancer; liver cancer; oral cancer; thyroid cancer; cervical cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; breast cancer; liver cancer; oral cancer; thyroid cancer; cervical cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
endometrial hyperplasia; endometrial neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease endometrial hyperplasia; endometrial neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, endometrioid; endometrial hyperplasia; endometrial neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, endometrioid; endometrial hyperplasia; endometrial neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast cancer; endometrial cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast cancer; endometrial cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal cancer; endometrial cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal cancer; endometrial cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; colorectal cancer; esophageal cancer; head and neck cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; colorectal cancer; esophageal cancer; head and neck cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; breast cancer; bladder cancer; cervical cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; breast cancer; bladder cancer; cervical cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; esophageal cancer; stomach cancer; bladder cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; esophageal cancer; stomach cancer; bladder cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; esophageal cancer; stomach cancer; bladder cancer; warfarin sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; esophageal cancer; stomach cancer; bladder cancer; warfarin sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast cancer; colorectal cancer; esophageal cancer; stomach cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast cancer; colorectal cancer; esophageal cancer; stomach cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypopharyngeal cancer; laryngeal cancer; oral cancer; oropharynx cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypopharyngeal cancer; laryngeal cancer; oral cancer; oropharynx cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia; lung cancer; laryngeal cancer; bladder cancer; oral-pharyngeal cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia; lung cancer; laryngeal cancer; bladder cancer; oral-pharyngeal cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; colorectal cancer; esophageal cancer; stomach cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; colorectal cancer; esophageal cancer; stomach cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
endometrial cancer Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease endometrial cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
endometrial cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease endometrial cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
endometrial cancer; hyperinsulinemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease endometrial cancer; hyperinsulinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
endometrial cancer risk. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease endometrial cancer risk. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
endometrial cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease endometrial cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Endometrial cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Endometrial cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
endometrial cancer Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease endometrial cancer in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
endometrial cancer Gene SetFrom KEGG Pathways proteins participating in the endometrial cancer pathway from the KEGG Pathways dataset. |
{endometrial cancer, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {endometrial cancer, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
uterine endometrial cancer cell Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue uterine endometrial cancer cell from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
endometrial cancer cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue endometrial cancer cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
uterine endometrial cancer cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue uterine endometrial cancer cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Recurrent Endometrial Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Endometrial Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Endometrial Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Endometrial Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Endometrial cancer Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Endometrial cancer pathway from the WikiPathways Pathways 2024 dataset. |
Endometrial cancer Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Endometrial cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Endometrial cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Endometrial cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Ovarian endometrial cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ovarian endometrial cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Uterine endometrial cancer cell Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Uterine endometrial cancer cell from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Endometrial cancer cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Endometrial cancer cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Uterine endometrial cancer cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Uterine endometrial cancer cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Endometrial cancer Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Endometrial cancer phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Colorectal / endometrial cancer Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Colorectal / endometrial cancer phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Endometrial cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Endometrial cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Colorectal or endometrial cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Colorectal or endometrial cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Endometrial cancer (endometrioid histology) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Endometrial cancer (endometrioid histology) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Endometrial cancer (Non-endometrioid histology) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Endometrial cancer (Non-endometrioid histology) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Endometriosis or endometrial cancer (pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Endometriosis or endometrial cancer (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Endometrial cancer Gene SetFrom KEGG Pathways 2026 proteins participating in the Endometrial cancer pathway from the KEGG Pathways 2026 dataset. |
leukemia; lung cancer; oropharyngolaryngeal cancers; laryngeal cancer; bladder cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia; lung cancer; oropharyngolaryngeal cancers; laryngeal cancer; bladder cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; breast cancer; colorectal cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; breast cancer; colorectal cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast cancer; colorectal cancer; liver cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast cancer; colorectal cancer; liver cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal cancer; drug hypersensitivity; liver cancer; bladder cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal cancer; drug hypersensitivity; liver cancer; bladder cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis, alcoholic; esophageal cancer; head and neck cancer; liver cancer; pancreatitis, alcoholic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis, alcoholic; esophageal cancer; head and neck cancer; liver cancer; pancreatitis, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
stomach cancer; pancreatic cancer; fallopian cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease stomach cancer; pancreatic cancer; fallopian cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; esophageal cancer; stomach cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; esophageal cancer; stomach cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal cancer; laryngeal cancer; oropharynx cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal cancer; laryngeal cancer; oropharynx cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
urethral cancer; brain cancer; colorectal cancer Gene SetFrom PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease urethral cancer; brain cancer; colorectal cancer from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset. |
Breast cancer, ovarian cancer or prostate cancer (pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Breast cancer, ovarian cancer or prostate cancer (pleiotropy) 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. |
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. |
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. |
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. |
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. |
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 colorectal cancer Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial colorectal cancer 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
{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. |
{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. |
{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. |
{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. |
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. |
{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. |
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. |
Breast Cancer, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Breast Cancer, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Non-Medullary Thyroid Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Non-Medullary Thyroid Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cutaneous Telangiectasia And Cancer Syndrome, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cutaneous Telangiectasia And Cancer Syndrome, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Nonmedullary Thyroid Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Nonmedullary Thyroid Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Breast Cancer, Familial Male Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Breast Cancer, Familial Male in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial cancer of breast Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial cancer of breast phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Familial colorectal cancer Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial colorectal cancer phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Familial ovarian cancer Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial ovarian cancer phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Familial prostate cancer Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial prostate cancer phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
BRIP1-associated familial cancer predisposition Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the BRIP1-associated familial cancer predisposition phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Familial breast and ovarian cancer Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial breast and ovarian cancer phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Familial lung cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Familial lung cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Endometrial carcinoma Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Endometrial carcinoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Endometrial Neoplasms Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Endometrial Neoplasms from the curated CTD Gene-Disease Associations dataset. |
Endometrial Hyperplasia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Endometrial Hyperplasia from the curated CTD Gene-Disease Associations dataset. |
Endometrial Neoplasms Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Endometrial Neoplasms in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
endometrial stromal sarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease endometrial stromal sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
endometrial adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease endometrial adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
endometrial carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease endometrial carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
endometrial mucinous adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease endometrial mucinous adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
endometrial clear cell adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease endometrial clear cell adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
endometrial disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease endometrial disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
endometrial stromal tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease endometrial stromal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
mixed endometrial stromal and smooth muscle tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mixed endometrial stromal and smooth muscle tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
endometrial squamous cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease endometrial squamous cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
endometrial transitional cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease endometrial transitional cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
endometrial adenosquamous carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease endometrial adenosquamous carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
endometrial small cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease endometrial small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
endometrial stromal nodule Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease endometrial stromal nodule in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
breast neoplasms; endometrial neoplasms; glucose intolerance; insulin resistance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms; endometrial neoplasms; glucose intolerance; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
endometrial adenocarcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease endometrial adenocarcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; endometrial neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; endometrial neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cervical neoplasm; endometrial neoplasms; radiation injuries; uterine cervical neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cervical neoplasm; endometrial neoplasms; radiation injuries; uterine cervical neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma; endometrial neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma; endometrial neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
endometrial carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease endometrial carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
endometrial neoplasms; neoplasms, hormone-dependent Gene SetFrom GAD Gene-Disease Associations genes associated with the disease endometrial neoplasms; neoplasms, hormone-dependent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
endometrial neoplasms; obesity; uterine neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease endometrial neoplasms; obesity; uterine neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cervical neoplasm; endometrial neoplasms; ovarian neoplasm; ovarian neoplasms; uterine cervical neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cervical neoplasm; endometrial neoplasms; ovarian neoplasm; ovarian neoplasms; uterine cervical neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms; hereditary nonpolyposis colorectal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms; hereditary nonpolyposis colorectal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
endometrial neoplasms; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease endometrial neoplasms; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, endometrioid; endometrial neoplasms; microsatellite instability Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, endometrioid; endometrial neoplasms; microsatellite instability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, renal cell; endometrial neoplasms; kidney neoplasms; neoplasms; renal cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, renal cell; endometrial neoplasms; kidney neoplasms; neoplasms; renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast neoplasms; colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms; colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma; endometrial neoplasms; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma; endometrial neoplasms; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus type ii; diabetes mellitus, type 2; endometrial neoplasms; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; endometrial neoplasms; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
endometrial neoplasms; neoplasm invasiveness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease endometrial neoplasms; neoplasm invasiveness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; endometrial neoplasms; microsatellite instability; neoplasm invasiveness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; endometrial neoplasms; microsatellite instability; neoplasm invasiveness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, endometrioid; endometrial neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, endometrioid; endometrial neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
endometrial neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease endometrial neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma; disease susceptibility; endometrial neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma; disease susceptibility; endometrial neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
uterine endometrial carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease uterine endometrial carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
endometrial neoplasms; insulin resistance; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease endometrial neoplasms; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, endometrioid; endometrial neoplasms; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, endometrioid; endometrial neoplasms; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, squamous cell; endometrial neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, squamous cell; endometrial neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma, clear cell; adenocarcinoma, mucinous; cystadenocarcinoma, serous; endometrial neoplasms; ovarian neoplasm; ovarian neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma, clear cell; adenocarcinoma, mucinous; cystadenocarcinoma, serous; endometrial neoplasms; ovarian neoplasm; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
endometrial neoplasms; ovarian neoplasm; ovarian neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease endometrial neoplasms; ovarian neoplasm; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
endometrial neoplasms; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease endometrial neoplasms; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
endometrial Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term endometrial in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
endometrial carcinoma Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease endometrial carcinoma in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
endometrial carcinoma Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the endometrial carcinoma phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
endometrial carcinoma Gene SetFrom HPO Gene-Disease Associations genes associated with the endometrial carcinoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Endometrial Neoplasms Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Endometrial Neoplasms phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Endometrial Hyperplasia Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Endometrial Hyperplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Sarcoma, Endometrial Stromal Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Sarcoma, Endometrial Stromal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
abnormal endometrial gland development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal endometrial gland development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
enlarged endometrial glands Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the enlarged endometrial glands phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased endometrial carcinoma incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased endometrial carcinoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased endometrial gland number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased endometrial gland number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small endometrial glands Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small endometrial glands phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal endometrial gland number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal endometrial gland number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal endometrial gland morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal endometrial gland morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent endometrial glands Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent endometrial glands phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased endometrial gland number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased endometrial gland number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
endometrial carcinoma, somatic Gene SetFrom OMIM Gene-Disease Associations genes associated with the endometrial carcinoma, somatic phenotype from the curated OMIM Gene-Disease Associations dataset. |
endometrial stromal cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue endometrial stromal cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
endometrial gland Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue endometrial gland in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
endometrial cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue endometrial cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
endometrial spiral artery Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue endometrial spiral artery in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Endometrial Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Endometrial Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Endometrial Stromal Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Endometrial Stromal Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Endometrial Adenocarcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Endometrial Adenocarcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Endometrial Hyperplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Endometrial Hyperplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Endometrial Endometrioid Adenocarcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Endometrial Endometrioid Adenocarcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Endometrial Intraepithelial Neoplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Endometrial Intraepithelial Neoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Papillary Serous Endometrial Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Papillary Serous Endometrial Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Endometrial Carcinosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Endometrial Carcinosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atypical Endometrial Hyperplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atypical Endometrial Hyperplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Complex Atypical Endometrial Hyperplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Complex Atypical Endometrial Hyperplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Endometrial Clear Cell Adenocarcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Endometrial Clear Cell Adenocarcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Benign Endometrial Hyperplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Benign Endometrial Hyperplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Endometrial Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Endometrial Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stage I Endometrial Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stage I Endometrial Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Endometrial Cystic Hyperplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Endometrial Cystic Hyperplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Endometrial Polyp Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Endometrial Polyp in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Simple Endometrial Hyperplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Simple Endometrial Hyperplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Endometrial Stromal Sarcoma, High Grade Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Endometrial Stromal Sarcoma, High Grade in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Grade Endometrial Stromal Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Grade Endometrial Stromal Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Uterine Corpus High Grade Endometrial Stromal Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Uterine Corpus High Grade Endometrial Stromal Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mucinous Endometrial Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mucinous Endometrial Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Endometrial Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Endometrial Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Endometrial Stromal Tumors Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Endometrial Stromal Tumors in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Serous Endometrial Intraepithelial Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Serous Endometrial Intraepithelial Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Complex Endometrial Hyperplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Complex Endometrial Hyperplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Metastatic Endometrial Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Metastatic Endometrial Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Endometrial Adenoacanthoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Endometrial Adenoacanthoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Endometrial Polyp Benign Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Endometrial Polyp Benign in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Benign Endometrial Stromal Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Benign Endometrial Stromal Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Endometrial Stromal Nodule Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Endometrial Stromal Nodule in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Endometrial Small Cell Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Endometrial Small Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Endometrial Undifferentiated Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Endometrial Undifferentiated Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Endometrial Cyst Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Endometrial Cyst in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Endometrial Squamous Cell Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Endometrial Squamous Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stage, Endometrial Carcinoma Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Stage, Endometrial Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
ZBTB16-27035670-HESC-HUMAN-ENDOMETRIAL Gene SetFrom ChEA Transcription Factor Targets 2022 target genes of the ZBTB16-27035670-HESC-HUMAN-ENDOMETRIAL transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset. |
absent endometrial glands Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent endometrial glands phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased endometrial carcinoma incidence Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased endometrial carcinoma incidence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased endometrial gland number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased endometrial gland number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal endometrial gland morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal endometrial gland morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
enlarged endometrial glands Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the enlarged endometrial glands phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal endometrial gland development Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal endometrial gland development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
small endometrial glands Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the small endometrial glands phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased endometrial gland number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased endometrial gland number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Human - Adipose - L1 - Endometrial Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Adipose - L1 - Endometrial cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Endometrial stem cell_Endometrium_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Endometrial stem cell_Endometrium_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Endometrial progenitor cell_Endometrium_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Endometrial progenitor cell_Endometrium_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Endometrial stromal stem cell_Endometrium stroma_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Endometrial stromal stem cell_Endometrium stroma_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Endometrial stem cell_Uterus_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Endometrial stem cell_Uterus_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Endometrial stromal cell_Uterus_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Endometrial stromal cell_Uterus_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
BMP2 WNT4 FOXO1 pathway in primary endometrial stromal cell differentiation Gene SetFrom WikiPathways Pathways 2024 proteins participating in the BMP2 WNT4 FOXO1 pathway in primary endometrial stromal cell differentiation pathway from the WikiPathways Pathways 2024 dataset. |
Endometrial carcinoma Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Endometrial carcinoma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Endometrial carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Endometrial carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Endometrial adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Endometrial adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Endometrial disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Endometrial disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Endometrial hyperplasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Endometrial hyperplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Uterine corpus endometrial carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Uterine corpus endometrial carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Endometrial stromal tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Endometrial stromal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Endometrial stromal sarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Endometrial stromal sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Endometrial serous adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Endometrial serous adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Endometrial stromal nodule Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Endometrial stromal nodule in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Endometrial mixed adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Endometrial mixed adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Endometrial mucinous adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Endometrial mucinous adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Endometrial transitional cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Endometrial transitional cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Endometrial squamous cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Endometrial squamous cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Cervical endometrial stromal sarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cervical endometrial stromal sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Cervix endometrial stromal tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cervix endometrial stromal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Endometrial adenosquamous carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Endometrial adenosquamous carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Endometrial clear cell adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Endometrial clear cell adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Endometrial small cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Endometrial small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Vaginal endometrial stromal sarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vaginal endometrial stromal sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Mixed endometrial stromal and smooth muscle tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed endometrial stromal and smooth muscle tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Vaginal endometrial stromal tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vaginal endometrial stromal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Endometrial cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Endometrial cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Endometrial stromal cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Endometrial stromal cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Endometrial gland Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Endometrial gland in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Uterine endometrial epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Uterine endometrial epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Uterine endometrial stromal sarcoma cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Uterine endometrial stromal sarcoma cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Endometrial glandular epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Endometrial glandular epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Endometrial luminal epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Endometrial luminal epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Endometrial luminal epithelial cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Endometrial luminal epithelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Endometrial gland cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Endometrial gland cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Endometrial spiral artery Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Endometrial spiral artery in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Endometrial carcinoma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Endometrial carcinoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Atypical endometrial hyperplasia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Atypical endometrial hyperplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Endometrial hyperplasia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Endometrial hyperplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Endometrial endometrioid carcinoma Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Endometrial endometrioid carcinoma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Hereditary cancer-predisposing syndrome:Hereditary cancer-predisposing syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary cancer-predisposing syndrome:Hereditary diffuse gastric cancer Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Hereditary diffuse gastric cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
PROSTATE CANCER/BRAIN CANCER SUSCEPTIBILITY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PROSTATE CANCER/BRAIN CANCER SUSCEPTIBILITY from the curated CTD Gene-Disease Associations dataset. |
cancer; colorectal cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cancer; colorectal cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal cancer; stomach cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal cancer; stomach cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ovarian cancer ; breast cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ovarian cancer ; breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal cancer; oropharyngolaryngeal cancers; stomach cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal cancer; oropharyngolaryngeal cancers; stomach cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal cancer; stomach cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal cancer; stomach cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colon cancer; rectal cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colon cancer; rectal cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast cancer; cytogenetic studies; prostate cancer; longevity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast cancer; cytogenetic studies; prostate cancer; longevity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; skin cancer, non-melanoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; skin cancer, non-melanoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
kidney cancer; bladder cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease kidney cancer; bladder cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast cancer; ovarian cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast cancer; ovarian cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal cancer; esophageal cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal cancer; esophageal cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; breast cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cancer; breast cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cancer; breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ovarian cancer; thyroid cancer; pheochromocytoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ovarian cancer; thyroid cancer; pheochromocytoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal cancer; gastric cardia cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal cancer; gastric cardia cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
liver cancer; nasopharyngeal cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease liver cancer; nasopharyngeal cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
prostate cancer ; breast cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease prostate cancer ; breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal cancer; stomach cancer; barret's esophagus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal cancer; stomach cancer; barret's esophagus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary duct stones; biliary tract cancer; gallbladder cancer; gallstones Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary duct stones; biliary tract cancer; gallbladder cancer; gallstones in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; bladder cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; bladder cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal cancer; gastric cardiac cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal cancer; gastric cardiac cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
stomach cancer; ovarian cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease stomach cancer; ovarian cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bladder cancer; prostate cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bladder cancer; prostate cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast cancer; colorectal cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast cancer; colorectal cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
prostate cancer; ovarian cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease prostate cancer; ovarian cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal cancer ; lung cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal cancer ; lung cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal cancer and lung cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal cancer and lung cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; liver cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; liver cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal cancer; cardiac cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal cancer; cardiac cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast cancer ovarian cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast cancer ovarian cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast cancer; prostate cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast cancer; prostate cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cancer; lung cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cancer; lung cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; esophageal cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; esophageal cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Esophageal cancer and gastric cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Esophageal cancer and gastric cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Multiple cancers (lung cancer, gastric cancer, and squamous cell carcinoma) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple cancers (lung cancer, gastric cancer, and squamous cell carcinoma) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
{prostate cancer/brain cancer susceptibility, somatic} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {prostate cancer/brain cancer susceptibility, somatic} phenotype from the curated OMIM Gene-Disease Associations dataset. |
breast cancer; colorectal cancer Gene SetFrom PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease breast cancer; colorectal cancer from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset. |
Inherited breast cancer and ovarian cancer Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Inherited breast cancer and ovarian cancer phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Prostate cancer/brain cancer susceptibility Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Prostate cancer/brain cancer susceptibility phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Multiple cancers (lung cancer, gastric cancer, and squamous cell carcinoma) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple cancers (lung cancer, gastric cancer, and squamous cell carcinoma) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Esophageal cancer and gastric cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Esophageal cancer and gastric cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Breast cancer and/or colorectal cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Breast cancer and/or colorectal cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Breast cancer in childhood cancer survivors treated with less than 10 gray radiotherapy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Breast cancer in childhood cancer survivors treated with less than 10 gray radiotherapy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Breast cancer in childhood cancer survivors treated with more than 10 gray radiotherapy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Breast cancer in childhood cancer survivors treated with more than 10 gray radiotherapy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Breast cancer in childhood cancer survivors Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Breast cancer in childhood cancer survivors phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 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. |
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 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. |
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. |
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 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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 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 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. |
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 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. |
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. |
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. |
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. |
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. |
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. |
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 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 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 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. |
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 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. |
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. |
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. |
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. |
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. |
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. |
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 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. |
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. |
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. |
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 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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 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 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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 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 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. |
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. |
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. |
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. |
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; 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. |
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. |
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. |
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. |
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. |
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. |
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 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. |
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 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 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; 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 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
advanced sleep-phase syndrome, familial, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the advanced sleep-phase syndrome, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
{meningioma, familial, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {meningioma, familial, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
epilepsy, myoclonic, familial adult, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the epilepsy, myoclonic, familial adult, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
?lipodystrophy, familial partial, type 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?lipodystrophy, familial partial, type 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
hypocalciuric hypercalcemia, familial, type iii Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypocalciuric hypercalcemia, familial, type iii phenotype from the curated OMIM Gene-Disease Associations dataset. |
short stature, idiopathic familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the short stature, idiopathic familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
candidiasis, familial, 1, autosomal dominant Gene SetFrom OMIM Gene-Disease Associations genes associated with the candidiasis, familial, 1, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset. |
periodic fever, familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the periodic fever, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyperfibrinolysis, familial, due to increased release of plat Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyperfibrinolysis, familial, due to increased release of plat phenotype from the curated OMIM Gene-Disease Associations dataset. |
{hypercholesterolemia, familial, modifier of} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {hypercholesterolemia, familial, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyperthyroidism, familial gestational Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyperthyroidism, familial gestational phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial abdominal, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial abdominal, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
migraine, familial hemiplegic Gene SetFrom OMIM Gene-Disease Associations genes associated with the migraine, familial hemiplegic phenotype from the curated OMIM Gene-Disease Associations dataset. |
alzheimer disease 1, familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the alzheimer disease 1, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyperproinsulinemia, familial, with or without diabetes Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyperproinsulinemia, familial, with or without diabetes phenotype from the curated OMIM Gene-Disease Associations dataset. |
vestibulopathy, familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the vestibulopathy, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
eosinophilia, familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the eosinophilia, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
candidiasis, familial, 2, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the candidiasis, familial, 2, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
x-inactivation, familial skewed Gene SetFrom OMIM Gene-Disease Associations genes associated with the x-inactivation, familial skewed phenotype from the curated OMIM Gene-Disease Associations dataset. |
familial cold autoinflammatory syndrome 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the familial cold autoinflammatory syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
convulsions, familial infantile, with paroxysmal choreoathetosis Gene SetFrom OMIM Gene-Disease Associations genes associated with the convulsions, familial infantile, with paroxysmal choreoathetosis phenotype from the curated OMIM Gene-Disease Associations dataset. |
trichoepithelioma, multiple familial, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the trichoepithelioma, multiple familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
trichoepithelioma, multiple familial, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the trichoepithelioma, multiple familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
myoclonus, familial cortical Gene SetFrom OMIM Gene-Disease Associations genes associated with the myoclonus, familial cortical phenotype from the curated OMIM Gene-Disease Associations dataset. |
acne inversa, familial, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the acne inversa, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
atrial fibrillation, familial, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
familial cold autoinflammatory syndrome 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the familial cold autoinflammatory syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
Familial (Fpah) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial (Fpah) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Alzheimer Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Alzheimer Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Lichen Amyloidosis Gene 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 Glucocorticoid Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Glucocorticoid Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Hdl Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Hdl Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Hypercholesterolemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Hypercholesterolemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypercholesterolemia, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypercholesterolemia, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypoalphalipoproteinemia, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypoalphalipoproteinemia, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Nuchal Bleb, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Nuchal Bleb, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Exudative Vitreoretinopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Exudative Vitreoretinopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Mediterranean Fever Gene 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 Intrahepatic Cholestasis Of Pregnancy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Intrahepatic Cholestasis Of Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Creutzfeldt-Jakob Disease, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Creutzfeldt-Jakob Disease, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Periodic Paralysis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Periodic Paralysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Primary Gastric Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Primary Gastric Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Pseudohyperkalemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Pseudohyperkalemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fatal Familial Insomnia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fatal Familial Insomnia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pseudohyperkalemia, Familial, 2, Due To Red Cell Leak Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pseudohyperkalemia, Familial, 2, Due To Red Cell Leak in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Dilated Cardiomyopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Dilated Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypoadrenocorticism, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypoadrenocorticism, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Thrombocytosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Thrombocytosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Osteochondritis Dissecans Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Osteochondritis Dissecans in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Generalized Lipodystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Generalized Lipodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Atypical Mole Melanoma Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Atypical Mole Melanoma Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Neurocardiogenic Syncope Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Neurocardiogenic Syncope in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Vesicoureteral Reflux Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Vesicoureteral Reflux in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Olivopontocerebellar Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Olivopontocerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Benign Hypercalcemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Benign Hypercalcemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Thoracic Aortic Aneurysm And Aortic Dissection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Thoracic Aortic Aneurysm And Aortic Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Benign Pemphigus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Benign Pemphigus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Cerebral Amyloid Angiopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Cerebral Amyloid Angiopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Hypophosphatemic Rickets Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Hypophosphatemic Rickets in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Visceral Myopathy, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Visceral Myopathy, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dysautonomia, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dysautonomia, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Paroxysmal Familial Ventricular Fibrillation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Paroxysmal Familial Ventricular Fibrillation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Hematuria Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Hematuria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Primary Pulmonary Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Primary Pulmonary Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Pulmonary Arterial Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Pulmonary Arterial Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Multiple Trichoepitheliomata Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Trichoepitheliomata in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atypical Mycobacteriosis, Familial, X-Linked 1 (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atypical Mycobacteriosis, Familial, X-Linked 1 (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Epilepsies Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Epilepsies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Thrombotic Thrombocytopenic Purpura Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Thrombotic Thrombocytopenic Purpura in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Ectopia Lentis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Ectopia Lentis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Idiopathic Hypercalciuria Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Idiopathic Hypercalciuria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chorea, Benign Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chorea, Benign Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dyskinesia, Familial, With Facial Myokymia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dyskinesia, Familial, With Facial Myokymia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Dermographism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Dermographism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Aplasia Of The Vermis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Aplasia Of The Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Partial Lipodystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Partial Lipodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Adenomatous Polyposis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Adenomatous Polyposis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Progressive Myoclonic Epilepsy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Progressive Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |