| Name |
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APC Geneadenomatous polyposis coli This gene encodes a tumor suppressor protein that acts as an antagonist of the Wnt signaling pathway. It is also involved in other processes including cell migration and adhesion, transcriptional activation, and apoptosis. Defects in this gene cause familial adenomatous polyposis (FAP), an autosomal dominant pre-malignant disease that usually progresses to malignancy. Mutations in the APC gene have been found to occur in most colorectal cancers, where disease-associated mutations tend to be clustered in a small region designated the mutation cluster region (MCR) and result in a truncated protein product. [provided by RefSeq, Jun 2022] |
AAA1 Geneaortic aneurysm, familial abdominal 1 |
AAA3 GeneAneurysm, familial abdominal 3 |
AAA2 GeneAortic aneurysm, familial abdominal 2 |
AAA4 GeneAortic aneurysm, familial abdominal, 4 |
ETL6 GeneEpilepsy, familial temporal lobe, 6 |
RCM2 Genecardiomyopathy, familial restrictive, 2 |
ATFB8 GeneAtrial fibrillation, familial, 8 |
HNFJ3 GeneHyperuricemic nephropathy, familial juvenile, 3 |
GPSC Genegliosis, familial progressive subcortical |
BHD GeneBeukes familial hip dysplasia |
FAME4 GeneEpilepsy, familial adult myoclonic, 4 |
FAME3 GeneEpilepsy, familial adult myoclonic, 3 |
PFHB2 GeneProgressive familial heart block, type II |
BFIS1 Genebenign familial infantile convulsions |
HBN1 GeneProgressive familial heart block, type I, locus 1 |
ETL2 Geneepilepsy, familial temporal lobe |
FHII GeneHyperaldosteronism, familial, type II |
FCMTE2 Genefamilial cortical myoclonic tremor with epilepsy 2 |
FCMTE1 Genefamilial cortical myoclonic tremor with epilepsy 1 |
GLM4 GeneGlioma, familial, 1 |
PSHK2 GenePseudohyperkalemia, familial, 2, due to red cell leak |
VVS GeneSyncope, familial vasovagal |
BFIS4 GeneConvulsions, benign familial infantile, 4 |
ATFB1 GeneAtrial fibrillation, familial 1 |
ATFB2 Genefamilial atrial fibrillation 2 |
SXI2 GeneX inactivation, familial skewed, 2 |
BFIC2 GeneBenign familial infantile convulsions-2 |
FMTLE GeneEpilepsy, familial mesial temporal lobe |
STUT3 GeneStuttering, familial persistent, 3 |
STUT2 GeneStuttering, familial persistent 2 |
STUT1 GeneStuttering, familial persistent 1 |
STUT4 GeneStuttering, familial persistent, 4 |
BRCD1 Genecancer, familial, with in vitro radioresistance |
MGR2 GeneMigraine, familial typical, susceptibility to |
MGR3 GeneMigraine, familial, with or without aura, susceptibility to |
MFT2 GeneTrichoepithelioma, multiple familial, 2 |
FEB9 GeneFebrile convulsions, familial, 9 |
ATFB5 GeneAtrial fibrillation, familial, 5 |
HTGS GeneHypertriglyceridemia, familial |
DIP Geneinterstitial pneumonitis, desquamative, familial |
CMH21 GeneCardiomyopathy, familial hypertrophic, 21 |
CANDF1 Genecandidiasis, familial 1 |
ATPLS Geneantiphospholipid syndrome, familial |
EOS Geneeosinophilia, familial |
FEB10 GeneFebrile convulsions, familial, 10 |
LVNC2 Genenoncompaction of left ventricular myocardium, familial isolated, autosomal dominant 2 |
THCYTX GeneThrombocytosis, familial X-linked |
CMS1A1 Genemyasthenia gravis, familial infantile, 1 |
BPPV Genevestibulopathy, familial |
AAT2 GeneAortic aneurysm, familial thoracic 2 |
AAT1 GeneAortic aneurysm, familial thoracic 1 |
NKCD GeneNatural killer cell deficiency, familial isolated |
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 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 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 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 Adenomatous Polyposis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Familial Adenomatous Polyposis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Familial adenomatous polyposis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Familial adenomatous polyposis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Familial adenomatous polyposis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial adenomatous polyposis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial adenomatous polyposis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial adenomatous polyposis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
adenomatous polyposis coli; adenomatous polyps Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenomatous polyposis coli; adenomatous polyps 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. |
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. |
late onset familial adenomatous polyposis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease late onset familial adenomatous polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Familial adenomatous polyposis 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial adenomatous polyposis 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial adenomatous polyposis 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial adenomatous polyposis 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial adenomatous polyposis 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial adenomatous polyposis 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Classic or attenuated familial adenomatous polyposis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Classic or attenuated familial adenomatous polyposis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
AXIN2-related attenuated familial adenomatous polyposis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the AXIN2-related attenuated familial adenomatous polyposis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
APC-related attenuated familial adenomatous polyposis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the APC-related attenuated familial adenomatous polyposis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Attenuated familial adenomatous polyposis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Attenuated familial adenomatous polyposis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Adenomatous polyposis coli:Gardner syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Adenomatous polyposis coli:Gardner syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Adenomatous polyposis coli Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Adenomatous polyposis coli phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Colorectal Adenomatous Polyposis, Autosomal Recessive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Colorectal Adenomatous Polyposis, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset. |
Adenomatous Polyposis Coli Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Adenomatous Polyposis Coli from the curated CTD Gene-Disease Associations dataset. |
adenomatous polyposis coli; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenomatous polyposis coli; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; adenomatous polyposis coli Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; adenomatous polyposis coli in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenomatous polyposis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenomatous polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenomatous polyposis coli; duodenal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenomatous polyposis coli; duodenal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenomatous polyposis coli; colorectal neoplasms; neoplasm recurrence, local Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenomatous polyposis coli; colorectal neoplasms; neoplasm recurrence, local in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenomatous polyposis coli Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenomatous polyposis coli in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenomatous polyposis coli; colorectal neoplasms; microsatellite instability Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenomatous polyposis coli; colorectal neoplasms; microsatellite instability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenomatous polyposis coli; colonic neoplasms; rectal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenomatous polyposis coli; colonic neoplasms; rectal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenomatous polyposis coli; cell transformation, neoplastic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenomatous polyposis coli; cell transformation, neoplastic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenomatous polyposis coli; fibromatosis, abdominal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenomatous polyposis coli; fibromatosis, abdominal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenomatous polyposis coli; colorectal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenomatous polyposis coli; colorectal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenomatous polyposis coli; colorectal neoplasms; intestinal polyps Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenomatous polyposis coli; colorectal neoplasms; intestinal polyps in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenomatous polyposis coli; bone neoplasms; epidermal cyst; gardner syndrome; gardner's syndrome; osteoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenomatous polyposis coli; bone neoplasms; epidermal cyst; gardner syndrome; gardner's syndrome; osteoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenomatous polyposis coli; colonic polyps Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenomatous polyposis coli; colonic polyps in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenomatous polyposis coli; rectal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenomatous polyposis coli; rectal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenomatous polyposis coli; duodenal neoplasms; jejunal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenomatous polyposis coli; duodenal neoplasms; jejunal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenomatous polyposis coli; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenomatous polyposis coli; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenoma; adenomatous polyposis coli; colorectal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenoma; adenomatous polyposis coli; colorectal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenomatous polyposis coli; microsatellite instability Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenomatous polyposis coli; microsatellite instability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenomatous colonic polyposis Gene SetFrom HPO Gene-Disease Associations genes associated with the adenomatous colonic polyposis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Adenomatous Polyposis Coli Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Adenomatous Polyposis Coli phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Adenomatous polyposis coli (APC) family Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Adenomatous polyposis coli (APC) family protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Adenomatous polyposis coli protein, 15 residue repeat Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Adenomatous polyposis coli protein, 15 residue repeat protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Adenomatous polyposis coli 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Adenomatous polyposis coli 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Adenomatous polyposis coli protein basic domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Adenomatous polyposis coli protein basic domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Adenomatous polyposis coli domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Adenomatous polyposis coli domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Adenomatous polyposis coli protein, cysteine-rich repeat Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Adenomatous polyposis coli protein, cysteine-rich repeat protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Adenomatous polyposis coli Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Adenomatous polyposis coli protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
adenomatous polyposis coli Gene SetFrom OMIM Gene-Disease Associations genes associated with the adenomatous polyposis coli phenotype from the curated OMIM Gene-Disease Associations dataset. |
colorectal adenomatous polyposis, autosomal recessive, with pilomatricomas Gene SetFrom OMIM Gene-Disease Associations genes associated with the colorectal adenomatous polyposis, autosomal recessive, with pilomatricomas phenotype from the curated OMIM Gene-Disease Associations dataset. |
Adenomatous Polyposis Coli Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adenomatous Polyposis Coli in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polyposis, Adenomatous Intestinal Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polyposis, Adenomatous Intestinal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adenomatous Polyposis Coli With Congenital Cholesteatoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adenomatous Polyposis Coli With Congenital Cholesteatoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Colorectal Adenomatous Polyposis, Autosomal Recessive Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Colorectal Adenomatous Polyposis, Autosomal Recessive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adenomatous Colonic Polyposis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Adenomatous Colonic Polyposis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Adenomatous polyposis coli Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Adenomatous polyposis coli phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Adenomatous colonic polyposis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Adenomatous colonic polyposis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Colorectal adenomatous polyposis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Colorectal adenomatous polyposis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Polymerase proofreading-related adenomatous polyposis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Polymerase proofreading-related adenomatous polyposis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
juvenile polyposis syndrome; polyposis, gastric Gene SetFrom GAD Gene-Disease Associations genes associated with the disease juvenile polyposis syndrome; polyposis, gastric in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Polyposis Of Gastric Fundus Without Polyposis Coli Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polyposis Of Gastric Fundus Without Polyposis Coli in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Generalized juvenile polyposis/juvenile polyposis coli Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized juvenile polyposis/juvenile polyposis coli phenotype from the curated ClinVar Gene-Phenotype Associations 2025 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 Intestinal Polyposis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Intestinal Polyposis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial multiple polyposis syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial multiple polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Adenomatous Polyps Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Adenomatous Polyps from the curated CTD Gene-Disease Associations dataset. |
adenoma; adenomatous polyps; carcinoma; colonic neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenoma; adenomatous polyps; carcinoma; colonic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenoma; adenomatous polyps; colonic polyps; colorectal neoplasms; hyperplasia; magnesium deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenoma; adenomatous polyps; colonic polyps; colorectal neoplasms; hyperplasia; magnesium deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal adenomatous polyps and adenocarcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal adenomatous polyps and adenocarcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenomatous polyps; colonic polyps; rectal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenomatous polyps; colonic polyps; rectal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenomatous polyps; colonic polyps; colorectal neoplasms; hyperplasia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenomatous polyps; colonic polyps; colorectal neoplasms; hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenomatous polyps; colorectal neoplasms; hyperplasia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenomatous polyps; colorectal neoplasms; hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenoma; adenomatous polyps; colorectal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenoma; adenomatous polyps; colorectal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenomatous polyps; colorectal neoplasms; neoplasm recurrence, local Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenomatous polyps; colorectal neoplasms; neoplasm recurrence, local in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenomatous polyps; colonic polyps Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenomatous polyps; colonic polyps in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenomatous Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term adenomatous in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Adenomatous Polyps Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Adenomatous Polyps phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Adenomatous Polyps Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adenomatous Polyps in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Adenomatous Polyps Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Adenomatous Polyps in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adenomatous Polyp Of Colon Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adenomatous Polyp Of Colon in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adenomatous Goiter Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adenomatous Goiter in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cervix Adenomatous Polyp Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cervix Adenomatous Polyp in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Colorectal Adenomatous Polyp Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Colorectal Adenomatous Polyp in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atypical Adenomatous Lung Hyperplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atypical Adenomatous Lung Hyperplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adenomatous polyp of colon Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Adenomatous polyp of colon phenotype from the curated ClinVar Gene-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. |
Juvenile polyposis syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Juvenile polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
MYH-associated polyposis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the MYH-associated polyposis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Polyposis Syndrome, Hereditary Mixed, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Polyposis Syndrome, Hereditary Mixed, 2 from the curated CTD Gene-Disease Associations dataset. |
Intestinal Polyposis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Intestinal Polyposis from the curated CTD Gene-Disease Associations dataset. |
Juvenile Polyposis with Hereditary Hemorrhagic Telangiectasia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Juvenile Polyposis with Hereditary Hemorrhagic Telangiectasia from the curated CTD Gene-Disease Associations dataset. |
Juvenile polyposis syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Juvenile polyposis syndrome from the curated CTD Gene-Disease Associations dataset. |
nasal polyposis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nasal polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polyposis, juvenile Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polyposis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
gastrointestinal neoplasms; hht - hereditary hemorrhagic telangiectasia; intestinal polyposis; neoplastic syndromes, hereditary; telangiectasia, hereditary hemorrhagic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gastrointestinal neoplasms; hht - hereditary hemorrhagic telangiectasia; intestinal polyposis; neoplastic syndromes, hereditary; telangiectasia, hereditary hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
intestinal polyposis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease intestinal polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
juvenile polyposis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease juvenile polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms; intestinal polyposis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms; intestinal polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary non-polyposis colon cancer. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary non-polyposis colon cancer. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
non-allergic nasal polyposis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease non-allergic nasal polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polyposis Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term polyposis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
juvenile colonic polyposis Gene SetFrom HPO Gene-Disease Associations genes associated with the juvenile colonic polyposis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
nasal polyposis Gene SetFrom HPO Gene-Disease Associations genes associated with the nasal polyposis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
juvenile gastrointestinal polyposis Gene SetFrom HPO Gene-Disease Associations genes associated with the juvenile gastrointestinal polyposis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
intestinal polyposis Gene SetFrom HPO Gene-Disease Associations genes associated with the intestinal polyposis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small intestinal polyposis Gene SetFrom HPO Gene-Disease Associations genes associated with the small intestinal polyposis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hyperplastic colonic polyposis Gene SetFrom HPO Gene-Disease Associations genes associated with the hyperplastic colonic polyposis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
duodenal polyposis Gene SetFrom HPO Gene-Disease Associations genes associated with the duodenal polyposis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
large intestinal polyposis Gene SetFrom HPO Gene-Disease Associations genes associated with the large intestinal polyposis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Intestinal Polyposis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Intestinal Polyposis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
polyposis, juvenile intestinal Gene SetFrom OMIM Gene-Disease Associations genes associated with the polyposis, juvenile intestinal phenotype from the curated OMIM Gene-Disease Associations dataset. |
brain tumor-polyposis syndrome 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the brain tumor-polyposis syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
polyposis syndrome, hereditary mixed, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the polyposis syndrome, hereditary mixed, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
juvenile polyposis syndrome, infantile form Gene SetFrom OMIM Gene-Disease Associations genes associated with the juvenile polyposis syndrome, infantile form phenotype from the curated OMIM Gene-Disease Associations dataset. |
Mutyh-Associate Polyposis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mutyh-Associate Polyposis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Intestinal Polyposis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Intestinal Polyposis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Juvenile Polyposis Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Juvenile Polyposis Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Brain Tumor-Polyposis Syndrome 2 (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Brain Tumor-Polyposis Syndrome 2 (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Duodenal Polyposis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Duodenal Polyposis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Juvenile Polyposis Coli Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Juvenile Polyposis Coli in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polyposis, Gastric Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polyposis, Gastric in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Non-Polyposis Colon Cancer Type 2 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Non-Polyposis Colon Cancer Type 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Non-Polyposis Colorectal Cancer Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Non-Polyposis Colorectal Cancer Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bmpr1A-Related Juvenile Polyposis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bmpr1A-Related Juvenile Polyposis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Juvenile Colonic Polyposis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Juvenile Colonic Polyposis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Juvenile Polyposis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Juvenile Polyposis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polyposis Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polyposis Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polyposis Syndrome, Hereditary Mixed, 2 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polyposis Syndrome, Hereditary Mixed, 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Smad4-Related Juvenile Polyposis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Smad4-Related Juvenile Polyposis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Serrated Hyperplastic Polyposis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Serrated Hyperplastic Polyposis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Large Intestinal Polyposis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Large Intestinal Polyposis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Juvenile Gastrointestinal Polyposis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Juvenile Gastrointestinal Polyposis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cap Polyposis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cap Polyposis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Colon Serrated Polyposis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Colon Serrated Polyposis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sessile Serrated Polyposis Cancer Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sessile Serrated Polyposis Cancer Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Juvenile polyposis syndrome Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Juvenile polyposis syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Juvenile polyposis syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Juvenile polyposis syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary mixed polyposis syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary mixed polyposis syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Juvenile polyposis-hereditary hemorrhagic telangiectasia syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Juvenile polyposis-hereditary hemorrhagic telangiectasia syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary mixed polyposis syndrome 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary mixed polyposis syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary mixed polyposis syndrome 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary mixed polyposis syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
APC-Associated Polyposis Disorders Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the APC-Associated Polyposis Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Brain tumor-polyposis syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Brain tumor-polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Duodenal polyposis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Duodenal polyposis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hyperplastic colonic polyposis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hyperplastic colonic polyposis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Gastric polyposis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Gastric polyposis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Inherited polyposis and early onset colorectal cancer - germline testing Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Inherited polyposis and early onset colorectal cancer - germline testing phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Juvenile polyposis syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Juvenile polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Polyposis syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Juvenile polyposis of stomach Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Juvenile polyposis of stomach phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Gastric adenocarcinoma and proximal polyposis of the stomach Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Gastric adenocarcinoma and proximal polyposis of the stomach phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Colorectal polyposis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Colorectal polyposis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
BMPR1A-Related Polyposis Syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the BMPR1A-Related Polyposis Syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
POLE-related polyposis and colorectal cancer syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the POLE-related polyposis and colorectal cancer syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Juvenile Polyposis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Juvenile Polyposis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Polymerase proofreading associated polyposis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Polymerase proofreading associated polyposis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Juvenile polyposis of infancy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Juvenile polyposis of infancy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Sessile serrated polyposis cancer syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Sessile serrated polyposis cancer syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hyperplastic polyposis syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hyperplastic polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hereditary mixed polyposis syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary mixed polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Bronchiectasis and nasal polyposis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Bronchiectasis and nasal polyposis phenotype from the curated ClinVar Gene-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 cancer of breast Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial cancer of breast phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial benign pemphigus Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial benign pemphigus phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Episodic pain syndrome, familial, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Episodic pain syndrome, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperpigmentation, familial progressive, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperpigmentation, familial progressive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial aortopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial aortopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Digital arthropathy-brachydactyly, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Digital arthropathy-brachydactyly, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Episodic pain syndrome, familial, 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Episodic pain syndrome, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Arrhythmogenic right ventricular dysplasia, familial, 13 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Febrile seizures, familial, 11 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Febrile seizures, familial, 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial benign hypercalcemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial benign hypercalcemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atrial fibrillation, familial, 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
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 colorectal cancer Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial colorectal cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial porphyria cutanea tarda Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial porphyria cutanea tarda phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hypertrophic cardiomyopathy 20 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 20 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Progressive familial intrahepatic cholestasis 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Progressive familial intrahepatic cholestasis 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Advanced sleep phase syndrome, familial, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Advanced sleep phase syndrome, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myoclonus, familial cortical Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myoclonus, familial cortical phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Migraine, familial basilar Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Migraine, familial basilar phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Breast-ovarian cancer, familial 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Breast-ovarian cancer, familial 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypercholanemia, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypercholanemia, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bone marrow failure, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bone marrow failure, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aortic aneurysm, familial thoracic 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Advanced sleep phase syndrome, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Advanced sleep phase syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Candidiasis, familial, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Candidiasis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Candidiasis, familial, 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Candidiasis, familial, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hypokalemia-hypomagnesemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial hypokalemia-hypomagnesemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myasthenia, limb-girdle, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myasthenia, limb-girdle, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atrial fibrillation, familial, 13 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atrial fibrillation, familial, 12 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atrial fibrillation, familial, 11 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atrial fibrillation, familial, 17 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atrial fibrillation, familial, 16 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atrial fibrillation, familial, 15 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hemophagocytic lymphohistiocytosis, familial, 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hemophagocytic lymphohistiocytosis, familial, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hemophagocytic lymphohistiocytosis, familial, 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hemophagocytic lymphohistiocytosis, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hemophagocytic lymphohistiocytosis, familial, 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hemophagocytic lymphohistiocytosis, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hemophagocytic lymphohistiocytosis, familial, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hemophagocytic lymphohistiocytosis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ventricular fibrillation, paroxysmal familial, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ventricular fibrillation, paroxysmal familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial platelet disorder with associated myeloid malignancy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial platelet disorder with associated myeloid malignancy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial erythrocytosis, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial erythrocytosis, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial medullary thyroid carcinoma Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial medullary thyroid carcinoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperinsulinemic hypoglycemia, familial, 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperinsulinemic hypoglycemia, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aortic aneurysm, familial thoracic 7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aortic aneurysm, familial thoracic 8 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aortic aneurysm, familial thoracic 9 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperlipidemia, familial combined Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperlipidemia, familial combined phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial amyloid polyneuropathy, Iowa type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial amyloid polyneuropathy, Iowa type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atrial fibrillation, familial, 14 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial encephalopathy with neuroserpin inclusion bodies Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial encephalopathy with neuroserpin inclusion bodies phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Epilepsy, familial adult myoclonic, 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, familial adult myoclonic, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atrial myxoma, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atrial myxoma, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lipodystrophy, familial partial, type 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lipodystrophy, familial partial, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lipodystrophy, familial partial, type 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lipodystrophy, familial partial, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypocalciuric hypercalcemia, familial, type 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypocalciuric hypercalcemia, familial, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypocalciuric hypercalcemia, familial, type 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypocalciuric hypercalcemia, familial, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial juvenile gout Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial juvenile gout phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cardiomyopathy:Familial hypertrophic cardiomyopathy 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy:Familial hypertrophic cardiomyopathy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypobetalipoproteinemia, familial, associated with apob32 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypobetalipoproteinemia, familial, associated with apob32 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Breast-ovarian cancer, familial 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Breast-ovarian cancer, familial 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atrial fibrillation, familial, 7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary cancer-predisposing syndrome:Erythrocytosis, familial, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Erythrocytosis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary familial hypertrophic cardiomyopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary familial hypertrophic cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial type 3 hyperlipoproteinemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial type 3 hyperlipoproteinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Tumoral calcinosis, familial, normophosphatemic Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Tumoral calcinosis, familial, normophosphatemic phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cd8 deficiency, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cd8 deficiency, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial infantile myasthenia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial infantile myasthenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked familial atypical mycobacteriosis, type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked familial atypical mycobacteriosis, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperthyroxinemia, familial dysalbuminemic Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperthyroxinemia, familial dysalbuminemic phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial type 5 hyperlipoproteinemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial type 5 hyperlipoproteinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cutaneous telangiectasia and cancer syndrome, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cutaneous telangiectasia and cancer syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial renal glucosuria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial renal glucosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial pulmonary capillary hemangiomatosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial pulmonary capillary hemangiomatosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hypoalphalipoproteinemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial hypoalphalipoproteinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial renal hypouricemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial renal hypouricemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
HYPERALDOSTERONISM, FAMILIAL, TYPE III Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the HYPERALDOSTERONISM, FAMILIAL, TYPE III phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myoclonic epilepsy, familial infantile Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myoclonic epilepsy, familial infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hypoplastic, glomerulocystic kidney Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial hypoplastic, glomerulocystic kidney phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial cold urticaria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial cold urticaria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aortic Aneurysm, Familial Abdominal 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Abdominal 2 from the curated CTD Gene-Disease Associations dataset. |
Familial myelofibrosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial myelofibrosis from the curated CTD Gene-Disease Associations dataset. |
Nephronophthisis, familial juvenile Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Nephronophthisis, familial juvenile from the curated CTD Gene-Disease Associations dataset. |
Eosinophilia, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Eosinophilia, Familial from the curated CTD Gene-Disease Associations dataset. |
Hyperlipidemia, Familial Combined Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyperlipidemia, Familial Combined from the curated CTD Gene-Disease Associations dataset. |
Platelet Disorder, Familial, with Associated Myeloid Malignancy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Platelet Disorder, Familial, with Associated Myeloid Malignancy from the curated CTD Gene-Disease Associations dataset. |
Hyperinsulinemic hypoglycemia, familial, 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyperinsulinemic hypoglycemia, familial, 6 from the curated CTD Gene-Disease Associations dataset. |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset. |
Pemphigus, Benign Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pemphigus, Benign Familial from the curated CTD Gene-Disease Associations dataset. |
Cardiomyopathy, Familial Restrictive, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 1 from the curated CTD Gene-Disease Associations dataset. |
Cardiomyopathy, Familial Hypertrophic, 9 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 9 from the curated CTD Gene-Disease Associations dataset. |
Cardiomyopathy, Familial Hypertrophic, 8 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 8 from the curated CTD Gene-Disease Associations dataset. |
Cardiomyopathy, Familial Hypertrophic, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 2 from the curated CTD Gene-Disease Associations dataset. |
Cardiomyopathy, Familial Hypertrophic, 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 6 from the curated CTD Gene-Disease Associations dataset. |
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. |
Cancer, Familial, with In Vitro Radioresistance Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cancer, Familial, with In Vitro Radioresistance from the curated CTD Gene-Disease Associations dataset. |
Febrile Convulsions, Familial, 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 5 from the curated CTD Gene-Disease Associations dataset. |
Hypoparathyroidism familial isolated Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypoparathyroidism familial isolated from the curated CTD Gene-Disease Associations dataset. |
Tumoral Calcinosis, Hyperphosphatemic, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Tumoral Calcinosis, Hyperphosphatemic, Familial from the curated CTD Gene-Disease Associations dataset. |
Atrial Fibrillation, Familial, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 3 from the curated CTD Gene-Disease Associations dataset. |
Hidradenitis suppurativa, familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hidradenitis suppurativa, familial from the curated CTD Gene-Disease Associations dataset. |
Dementia, familial Danish Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Dementia, familial Danish from the curated CTD Gene-Disease Associations dataset. |
Familial medullary thyroid carcinoma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial medullary thyroid carcinoma from the curated CTD Gene-Disease Associations dataset. |
Interstitial Pneumonitis, Desquamative, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Interstitial Pneumonitis, Desquamative, Familial from the curated CTD Gene-Disease Associations dataset. |
Hemophagocytic lymphohistiocytosis, familial, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hemophagocytic lymphohistiocytosis, familial, 4 from the curated CTD Gene-Disease Associations dataset. |
Pseudohyperkalemia, Familial, 2, due to Red Cell Leak Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pseudohyperkalemia, Familial, 2, due to Red Cell Leak from the curated CTD Gene-Disease Associations dataset. |
Cirrhosis, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cirrhosis, Familial from the curated CTD Gene-Disease Associations dataset. |
Familial encephalopathy with neuroserpin inclusion bodies Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial encephalopathy with neuroserpin inclusion bodies from the curated CTD Gene-Disease Associations dataset. |
Lipodystrophy, Familial Partial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lipodystrophy, Familial Partial from the curated CTD Gene-Disease Associations dataset. |
Cardiomyopathy, Familial Restrictive, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 3 from the curated CTD Gene-Disease Associations dataset. |
Familial 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. |
Prostate cancer, familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prostate cancer, familial from the curated CTD Gene-Disease Associations dataset. |
Convulsions, Benign Familial Infantile, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Convulsions, Benign Familial Infantile, 4 from the curated CTD Gene-Disease Associations dataset. |
Polycythemia, primary familial and congenital Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Polycythemia, primary familial and congenital from the curated CTD Gene-Disease Associations dataset. |
PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA from the curated CTD Gene-Disease Associations dataset. |
Aortic Aneurysm, Familial Thoracic 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 1 from the curated CTD Gene-Disease Associations dataset. |
Erythrocytosis, Familial, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Erythrocytosis, Familial, 4 from the curated CTD Gene-Disease Associations dataset. |
Hyperinsulinemic hypoglycemia, familial, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyperinsulinemic hypoglycemia, familial, 3 from the curated CTD Gene-Disease Associations dataset. |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset. |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset. |
Hyperinsulinemic hypoglycemia, familial, 7 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyperinsulinemic hypoglycemia, familial, 7 from the curated CTD Gene-Disease Associations dataset. |
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7 from the curated CTD Gene-Disease Associations dataset. |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 from the curated CTD Gene-Disease Associations dataset. |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 from the curated CTD Gene-Disease Associations dataset. |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 from the curated CTD Gene-Disease Associations dataset. |
Hyperthyroxinemia, Familial Dysalbuminemic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyperthyroxinemia, Familial Dysalbuminemic from the curated CTD Gene-Disease Associations dataset. |
Aortic aneurysm, familial thoracic 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic aneurysm, familial thoracic 4 from the curated CTD Gene-Disease Associations dataset. |
Cardiomyopathy, Familial Restrictive, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 2 from the curated CTD Gene-Disease Associations dataset. |
Atrial Fibrillation, Familial, 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 5 from the curated CTD Gene-Disease Associations dataset. |
Familial cylindromatosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial cylindromatosis from the curated CTD Gene-Disease Associations dataset. |
Familial benign hypercalcemia, type 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial benign hypercalcemia, type 3 from the curated CTD Gene-Disease Associations dataset. |
Hyperaldosteronism, Familial, Type II Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyperaldosteronism, Familial, Type II from the curated CTD Gene-Disease Associations dataset. |
Cardiomyopathy, Familial Hypertrophic, 11 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 11 from the curated CTD Gene-Disease Associations dataset. |
Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia from the curated CTD Gene-Disease Associations dataset. |
Atrial myxoma, familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Atrial myxoma, familial from the curated CTD Gene-Disease Associations dataset. |
Familial Glucocorticoid Deficiency 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial Glucocorticoid Deficiency 1 from the curated CTD Gene-Disease Associations dataset. |
Tumoral Calcinosis, Normophosphatemic, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Tumoral Calcinosis, Normophosphatemic, Familial from the curated CTD Gene-Disease Associations dataset. |
MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset. |
Hypocalciuric hypercalcemia, familial, type 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypocalciuric hypercalcemia, familial, type 1 from the curated CTD Gene-Disease Associations dataset. |
Trichoepithelioma multiple familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Trichoepithelioma multiple familial from the curated CTD Gene-Disease Associations dataset. |
Febrile Convulsions, Familial, 10 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 10 from the curated CTD Gene-Disease Associations dataset. |
EPILEPSY, FAMILIAL TEMPORAL LOBE, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 1 from the curated CTD Gene-Disease Associations dataset. |
EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2 from the curated CTD Gene-Disease Associations dataset. |
Hemophagocytic lymphohistiocytosis, familial, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hemophagocytic lymphohistiocytosis, familial, 2 from the curated CTD Gene-Disease Associations dataset. |
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 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 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. |
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 or sporadic prostate cancer. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial or sporadic prostate cancer. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial distal renal tubular acidosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial distal renal tubular acidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
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. |
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 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. |
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. |
breast cancer, familial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast cancer, familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis; hyperlipidemia, familial combined Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis; hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial hypertrophic cardiomyopathy. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial hypertrophic cardiomyopathy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial cataract Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial cataract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amyloid neuropathies, familial; constipation; diarrhea; gastrointestinal diseases; nausea; vomiting Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amyloid neuropathies, familial; constipation; diarrhea; gastrointestinal diseases; nausea; vomiting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
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. |
{breast-ovarian cancer, familial, 1} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {breast-ovarian cancer, familial, 1} phenotype from the curated OMIM Gene-Disease Associations dataset. |
digital arthropathy-brachydactyly, familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the digital arthropathy-brachydactyly, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
progressive familial heart block, type ib Gene SetFrom OMIM Gene-Disease Associations genes associated with the progressive familial heart block, type ib phenotype from the curated OMIM Gene-Disease Associations dataset. |
migraine, familial basilar Gene SetFrom OMIM Gene-Disease Associations genes associated with the migraine, familial basilar phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial thoracic 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial thoracic 6 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial thoracic 7 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 7 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial thoracic 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial thoracic 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial thoracic 8 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 8 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial thoracic 9 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 9 phenotype from the curated OMIM Gene-Disease Associations dataset. |
insomnia, fatal familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the insomnia, fatal familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
dysautonomia, familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the dysautonomia, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
febrile seizures, familial, 9 Gene SetFrom OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 9 phenotype from the curated OMIM Gene-Disease Associations dataset. |
febrile seizures, familial, 8 Gene SetFrom OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 8 phenotype from the curated OMIM Gene-Disease Associations dataset. |
febrile seizures, familial, 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
febrile seizures, familial, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
febrile seizures, familial, 7 Gene SetFrom OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 7 phenotype from the curated OMIM Gene-Disease Associations dataset. |
febrile seizures, familial, 6 Gene SetFrom OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
febrile seizures, familial, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
febrile seizures, familial, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
combined hyperlipidemia, familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the combined hyperlipidemia, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial abdominal 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial abdominal 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial abdominal 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial abdominal 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
familial cold-induced inflammatory syndrome 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the familial cold-induced inflammatory syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
febrile seizures, familial, 11 Gene SetFrom OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 11 phenotype from the curated OMIM Gene-Disease Associations dataset. |
febrile seizures, familial, 10 Gene SetFrom OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 10 phenotype from the curated OMIM Gene-Disease Associations dataset. |
epilepsy, familial temporal lobe, 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the epilepsy, familial temporal lobe, 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
epilepsy, familial temporal lobe, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the epilepsy, familial temporal lobe, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
epilepsy, familial temporal lobe, 6 Gene SetFrom OMIM Gene-Disease Associations genes associated with the epilepsy, familial temporal lobe, 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
epilepsy, familial temporal lobe, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the epilepsy, familial temporal lobe, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
epilepsy, familial temporal lobe, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the epilepsy, familial temporal lobe, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cardiomyopathy, familial hypertrophic, 19 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 19 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cardiomyopathy, familial hypertrophic, 18 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 18 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cardiomyopathy, familial hypertrophic, 11 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 11 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cardiomyopathy, familial hypertrophic, 10 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 10 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cardiomyopathy, familial hypertrophic, 13 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 13 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cardiomyopathy, familial hypertrophic, 12 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 12 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cardiomyopathy, familial hypertrophic, 15 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 15 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cardiomyopathy, familial hypertrophic, 14 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 14 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cardiomyopathy, familial hypertrophic, 16 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 16 phenotype from the curated OMIM Gene-Disease Associations dataset. |
hypobetalipoproteinemia, familial, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypobetalipoproteinemia, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
febrile seizures, familial, 3a Gene SetFrom OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 3a phenotype from the curated OMIM Gene-Disease Associations dataset. |
cardiomyopathy, familial hypertrophic 17 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic 17 phenotype from the curated OMIM Gene-Disease Associations dataset. |
dementia, familial danish Gene SetFrom OMIM Gene-Disease Associations genes associated with the dementia, familial danish phenotype from the curated OMIM Gene-Disease Associations dataset. |
cardiomyopathy, familial hypertrophic 6 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
seizures, benign familial infantile, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
seizures, benign familial infantile, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
seizures, benign familial infantile, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
seizures, benign familial infantile, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
[igg receptor i, phagocytic, familial deficiency of] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [igg receptor i, phagocytic, familial deficiency of] phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyperuricemic nephropathy, familial juvenile 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyperuricemic nephropathy, familial juvenile 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
{breast-ovarian cancer, familial, susceptibility to, 4} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {breast-ovarian cancer, familial, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyperaldosteronism, familial, type iii Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyperaldosteronism, familial, type iii phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyperinsulinemic hypoglycemia, familial, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyperinsulinemic hypoglycemia, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyperinsulinemic hypoglycemia, familial, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyperinsulinemic hypoglycemia, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyperinsulinemic hypoglycemia, familial, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyperinsulinemic hypoglycemia, familial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyperinsulinemic hypoglycemia, familial, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyperinsulinemic hypoglycemia, familial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyperinsulinemic hypoglycemia, familial, 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyperinsulinemic hypoglycemia, familial, 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyperinsulinemic hypoglycemia, familial, 7 Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyperinsulinemic hypoglycemia, familial, 7 phenotype from the curated OMIM Gene-Disease Associations dataset. |
?epilepsy, familial adult myoclonic, 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?epilepsy, familial adult myoclonic, 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
?candidiasis, familial, 8 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?candidiasis, familial, 8 phenotype from the curated OMIM Gene-Disease Associations dataset. |
[fleck retina, familial benign] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [fleck retina, familial benign] phenotype from the curated OMIM Gene-Disease Associations dataset. |
cardiomyopathy, familial hypertrophic, 21 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 21 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cardiomyopathy, familial hypertrophic, 22 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 22 phenotype from the curated OMIM Gene-Disease Associations dataset. |
candidiasis, familial, 6, autosomal dominant Gene SetFrom OMIM Gene-Disease Associations genes associated with the candidiasis, familial, 6, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset. |
carpal tunnel syndrome, familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the carpal tunnel syndrome, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
atrial fibrillation, familial, 13 Gene SetFrom OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 13 phenotype from the curated OMIM Gene-Disease Associations dataset. |
atrial fibrillation, familial, 12 Gene SetFrom OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 12 phenotype from the curated OMIM Gene-Disease Associations dataset. |
atrial fibrillation, familial, 11 Gene SetFrom OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 11 phenotype from the curated OMIM Gene-Disease Associations dataset. |
atrial fibrillation, familial, 10 Gene SetFrom OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 10 phenotype from the curated OMIM Gene-Disease Associations dataset. |
atrial fibrillation, familial, 17 Gene SetFrom OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 17 phenotype from the curated OMIM Gene-Disease Associations dataset. |
atrial fibrillation, familial, 16 Gene SetFrom OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 16 phenotype from the curated OMIM Gene-Disease Associations dataset. |
atrial fibrillation, familial, 14 Gene SetFrom OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 14 phenotype from the curated OMIM Gene-Disease Associations dataset. |
medullary thyroid carcinoma, familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the medullary thyroid carcinoma, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
hypercholesterolemia, familial, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypercholesterolemia, familial, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
ventricular fibrillation, paroxysmal familial, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ventricular fibrillation, paroxysmal familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cardiomyopathy, familial hypertrophic, 9 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 9 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cardiomyopathy, familial hypertrophic, 8 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 8 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cardiomyopathy, familial hypertrophic, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cardiomyopathy, familial hypertrophic, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cardiomyopathy, familial hypertrophic, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cardiomyopathy, familial hypertrophic, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cardiomyopathy, familial hypertrophic, 7 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 7 phenotype from the curated OMIM Gene-Disease Associations dataset. |
acne inversa, familial, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the acne inversa, familial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
endometrial cancer, familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the endometrial cancer, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyperbilirubinemia, familial transient neonatal Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyperbilirubinemia, familial transient neonatal phenotype from the curated OMIM Gene-Disease Associations dataset. |
dementia, familial, nonspecific Gene SetFrom OMIM Gene-Disease Associations genes associated with the dementia, familial, nonspecific phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyperuricemic nephropathy, familial juvenile 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyperuricemic nephropathy, familial juvenile 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyperuricemic nephropathy, familial juvenile, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyperuricemic nephropathy, familial juvenile, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyperaldosteronism, familial, type ii Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyperaldosteronism, familial, type ii phenotype from the curated OMIM Gene-Disease Associations dataset. |
lipodystrophy, familial partial, type 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the lipodystrophy, familial partial, type 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
lipodystrophy, familial partial, type 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the lipodystrophy, familial partial, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
hemophagocytic lymphohistiocytosis, familial, 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the hemophagocytic lymphohistiocytosis, familial, 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
hemophagocytic lymphohistiocytosis, familial, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the hemophagocytic lymphohistiocytosis, familial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
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. |
{breast-ovarian cancer, familial, 2} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {breast-ovarian cancer, familial, 2} phenotype from the curated OMIM Gene-Disease Associations dataset. |
cardiomyopathy, familial restrictive, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial restrictive, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cardiomyopathy, familial restrictive, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial restrictive, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cardiomyopathy, familial restrictive, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial restrictive, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cardiomyopathy, familial restrictive, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial restrictive, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
candidiasis, familial, 5, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the candidiasis, familial, 5, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
hypercholanemia, familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypercholanemia, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
candidiasis, familial, 4, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the candidiasis, familial, 4, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
myasthenia, familial infantile, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the myasthenia, familial infantile, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
{prostate cancer, familial, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {prostate cancer, familial, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
episodic pain syndrome, familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the episodic pain syndrome, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
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. |
gastric cancer, familial diffuse, with or without cleft lip and/or palate Gene SetFrom OMIM Gene-Disease Associations genes associated with the gastric cancer, familial diffuse, with or without cleft lip and/or palate phenotype from the curated OMIM Gene-Disease Associations dataset. |
lipodystrophy, familial partial, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the lipodystrophy, familial partial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
{coronary artery disease in familial hypercholesterolemia, protection against} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {coronary artery disease in familial hypercholesterolemia, protection against} phenotype from the curated OMIM Gene-Disease Associations dataset. |
thrombotic thrombocytopenic purpura, familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the thrombotic thrombocytopenic purpura, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
osteolysis, familial expansile Gene SetFrom OMIM Gene-Disease Associations genes associated with the osteolysis, familial expansile phenotype from the curated OMIM Gene-Disease Associations dataset. |
myoclonic epilepsy, infantile, familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the myoclonic epilepsy, infantile, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
hypercholesterolemia, familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypercholesterolemia, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
[gamma-glutamyltransferase, familial high serum] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [gamma-glutamyltransferase, familial high serum] phenotype from the curated OMIM Gene-Disease Associations dataset. |
cardiomyopathy, familial hypertrophic Gene SetFrom OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic phenotype from the curated OMIM Gene-Disease Associations dataset. |
{breast-ovarian cancer, familial, susceptibility to, 3} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {breast-ovarian cancer, familial, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset. |
acne inversa, familial, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the acne inversa, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
atrial fibrillation, familial, 9 Gene SetFrom OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 9 phenotype from the curated OMIM Gene-Disease Associations dataset. |
atrial fibrillation, familial, 8 Gene SetFrom OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 8 phenotype from the curated OMIM Gene-Disease Associations dataset. |
atrial fibrillation, familial, 7 Gene SetFrom OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 7 phenotype from the curated OMIM Gene-Disease Associations dataset. |
atrial fibrillation, familial, 6 Gene SetFrom OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
atrial fibrillation, familial, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
atrial fibrillation, familial, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
atrial fibrillation, familial, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
ectopia lentis, familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the ectopia lentis, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
platelet disorder, familial, with associated myeloid malignancy Gene SetFrom OMIM Gene-Disease Associations genes associated with the platelet disorder, familial, with associated myeloid malignancy phenotype from the curated OMIM Gene-Disease Associations dataset. |
cutaneous telangiectasia and cancer syndrome, familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the cutaneous telangiectasia and cancer syndrome, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
neurofibromatosis, familial spinal Gene SetFrom OMIM Gene-Disease Associations genes associated with the neurofibromatosis, familial spinal phenotype from the curated OMIM Gene-Disease Associations dataset. |
?familial cold autoinflammatory syndrome 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?familial cold autoinflammatory syndrome 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
renal cell carcinoma, papillary, 1, familial and somatic Gene SetFrom OMIM Gene-Disease Associations genes associated with the renal cell carcinoma, papillary, 1, familial and somatic phenotype from the curated OMIM Gene-Disease Associations dataset. |
cardiomyopathy, familial hypertrophic, 20 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 20 phenotype from the curated OMIM Gene-Disease Associations dataset. |
tumoral calcinosis, familial, normophosphatemic Gene SetFrom OMIM Gene-Disease Associations genes associated with the tumoral calcinosis, familial, normophosphatemic phenotype from the curated OMIM Gene-Disease Associations dataset. |
?antiphospholipid syndrome, familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?antiphospholipid syndrome, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
{hyperlipidemia, familial combined, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {hyperlipidemia, familial combined, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
tumoral calcinosis, hyperphosphatemic, familial Gene SetFrom OMIM Gene-Disease Associations genes associated with the tumoral calcinosis, hyperphosphatemic, familial phenotype from the curated OMIM Gene-Disease Associations dataset. |
arrhythmogenic right ventricular dysplasia, familial, 13 Gene SetFrom OMIM Gene-Disease Associations genes associated with the arrhythmogenic right ventricular dysplasia, familial, 13 phenotype from the curated OMIM Gene-Disease Associations dataset. |
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. |
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 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 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. |
Familial Hyperaldosteronism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Hyperaldosteronism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Sick Sinus Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Sick Sinus Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Patent Ductus Arteriosus Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Patent Ductus Arteriosus Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Guillain-Barre Syndrome, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Guillain-Barre Syndrome, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Acromegaly Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Acromegaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Non-Medullary Thyroid Cancer Gene 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. |
Somatotrophinoma, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Somatotrophinoma, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Danish Type Familial Amyloid Cardiomyopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Danish Type Familial Amyloid Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Lcat Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Lcat Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Juvenile Parkinsonism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Juvenile Parkinsonism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Autosomal Dominant Familial Dystonia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Autosomal Recessive Familial Dystonia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Dystonia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Idiopathic Familial Dystonia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Anhidrosis, Familial Generalized, With Abnormal Or Absent Sweat Glands Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Anhidrosis, Familial Generalized, With Abnormal Or Absent Sweat Glands in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Hypobetalipoproteinemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Hypobetalipoproteinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypobetalipoproteinemia, Familial, 2 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypobetalipoproteinemia, Familial, 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Chondrocalcinosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Chondrocalcinosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Platelet Disorder, Familial, With Associated Myeloid Malignancy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Platelet Disorder, Familial, With Associated Myeloid Malignancy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Gigantiform Cementoma, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Gigantiform Cementoma, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Nonmedullary Thyroid Gland Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Nonmedullary Thyroid Gland Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Medullary Thyroid Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Medullary Thyroid Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Hyperparathyroidism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Hyperparathyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Atypical Multiple Mole-Melanoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Atypical Multiple Mole-Melanoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dementia, Familial Danish Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dementia, Familial Danish in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Hyperalphalipoproteinemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Hyperalphalipoproteinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hyperchylomicronemia With Hyperprebetalipoproteinemia, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hyperchylomicronemia With Hyperprebetalipoproteinemia, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Lipoprotein Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Lipoprotein Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypercholesterolemia, Familial, Due To Ligand-Defective Apolipoprotein B Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypercholesterolemia, Familial, Due To Ligand-Defective Apolipoprotein B in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypobetalipoproteinemia, Familial, Apolipoprotein B Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypobetalipoproteinemia, Familial, Apolipoprotein B in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Apolipoprotein C-Ii Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Apolipoprotein C-Ii Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Amyloid Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Amyloid Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Dementia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Dementia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Testicular Germ Cell Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Testicular Germ Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Motor Neuron Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Motor Neuron Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Cervical Artery Dissection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Cervical Artery Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Erythrocytosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Erythrocytosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Collagenosis, Familial Reactive Perforating Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Collagenosis, Familial Reactive Perforating in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Tremor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Tremor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Benign Adult Familial Myoclonic Epilepsy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Benign Adult Familial Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Idiopathic Pulmonary Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Idiopathic Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Benign Neonatal Epilepsy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Benign Neonatal Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Hemiplegic Migraine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Hemiplegic Migraine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Migraine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Migraine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cutaneous Telangiectasia And Cancer Syndrome, Familial Gene 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 Alcoholism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Alcoholism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Central Diabetes Insipidus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Central Diabetes Insipidus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypercholanemia, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypercholanemia, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Cardiomyopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Renal Cell Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Renal Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Nonmedullary Thyroid Cancer Gene 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. |
Dermatitis Herpetiformis, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dermatitis Herpetiformis, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Colorectal Camcer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Colorectal Camcer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Hypertrophic Cardiomyopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Hypertrophic Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Breast Cancer, Familial Male Gene 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 Malignant Neoplasm Of Pancreas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Malignant Neoplasm Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Testotoxicosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Testotoxicosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hematuria, Benign Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hematuria, Benign Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Idiopathic Non-Familial Dystonia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Non-Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Ventricular Tachycardia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Ventricular Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Hemolytic Uremic Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Hemolytic Uremic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Psoriasis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Psoriasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Pityriasis Rubra Pilaris Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Pityriasis Rubra Pilaris in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Candidiasis, Familial, 2 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Candidiasis, Familial, 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Cold Urticaria Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Cold Urticaria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Isolated Hyperparathyroidism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Isolated Hyperparathyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Eosinophilia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Eosinophilia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Cerebral Cavernous Malformation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Cerebral Cavernous Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Atypical Hemolytic Uremic Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Atypical Hemolytic Uremic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Chronic Lymphocytic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Chronic Lymphocytic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cd8 Deficiency, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cd8 Deficiency, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Malignant Melanoma Of Skin Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Malignant Melanoma Of Skin in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Acute Myeloid Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Acute Myeloid Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Retinoblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Retinoblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Infantile Myasthenia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Infantile Myasthenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Charge Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Charge Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Benign Familial Convulsion Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Benign Familial Convulsion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Myasthenia, Familial Infantile, 1 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Myasthenia, Familial Infantile, 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Advanced Sleep-Phase Syndrome, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Advanced Sleep-Phase Syndrome, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Primary Hypomagnesemia With Normocalciuria And Normocalcemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Primary Hypomagnesemia With Normocalciuria And Normocalcemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Schizencephaly Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Schizencephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Vascular Leukoencephalopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Vascular Leukoencephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Multiple Factor Deficiency Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Factor Deficiency Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Apoceruloplasmin Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Apoceruloplasmin Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Benign Familial Mesial Temporal Lobe Epilepsy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Benign Familial Mesial Temporal Lobe Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Multiple Lipomatosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Lipomatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atypical Mycobacteriosis, Familial, X-Linked 2 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atypical Mycobacteriosis, Familial, X-Linked 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Amyloid Polyneuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Amyloid Polyneuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Hypoaldosteronism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Hypoaldosteronism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Mitral Valve Prolapse Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Mitral Valve Prolapse in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Reticuloendotheliosis, Familial, With Eosinophilia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Reticuloendotheliosis, Familial, With Eosinophilia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Temporal Epilepsy, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Temporal Epilepsy, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Noncompaction Of Left Ventricular Myocardium, Familial Isolated, Autosomal Dominant 1 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Noncompaction Of Left Ventricular Myocardium, Familial Isolated, Autosomal Dominant 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Dyshormonogenetic Goiter Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Dyshormonogenetic Goiter in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Thyroid Dyshormonogenesis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Thyroid Dyshormonogenesis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hidradenitis Suppurativa, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hidradenitis Suppurativa, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Polycythemia Vera Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Polycythemia Vera in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polyneuropathy, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polyneuropathy, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Lambdoid Synostosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Lambdoid Synostosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Premature Ovarian Failure, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Premature Ovarian Failure, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Antiphospholipid Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Antiphospholipid Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Hypophosphatemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Hypophosphatemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Isolated Trichomegaly Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Isolated Trichomegaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Acanthosis Nigricans Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Acanthosis Nigricans in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Multiple Trichodiscomas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Multiple Trichodiscomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Spontaneous Pneumothorax Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Spontaneous Pneumothorax in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Restrictive Cardiomyopathy (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Restrictive Cardiomyopathy (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dandy-Walker Syndrome, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dandy-Walker Syndrome, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ovarian Hyperstimulation Syndrome, Familial Gestational Spontaneous Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ovarian Hyperstimulation Syndrome, Familial Gestational Spontaneous in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Acute Myeloid Leukemia With Mutated Cebpa Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Acute Myeloid Leukemia With Mutated Cebpa in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Bicuspid Aortic Valve Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Bicuspid Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrophia Maculosa Varioliformis Cutis, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophia Maculosa Varioliformis Cutis, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Familial Brain Calcification Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Familial Brain Calcification in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Hyperekplexia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Hyperekplexia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Nevi Flammei, Familial Multiple Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Nevi Flammei, Familial Multiple in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hyperpotassemia And Hypertension, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hyperpotassemia And Hypertension, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Eunuchoidism, Familial Hypogonadotropic Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Eunuchoidism, Familial Hypogonadotropic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |