Name

Familial Intestinal Polyposis Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Familial Intestinal Polyposis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

juvenile polyposis syndrome; polyposis, gastric Gene Set

From 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 Set

From 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 Set

From 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.

Intestinal Polyposis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Intestinal Polyposis from the curated CTD Gene-Disease Associations dataset.

gastrointestinal neoplasms; hht - hereditary hemorrhagic telangiectasia; intestinal polyposis; neoplastic syndromes, hereditary; telangiectasia, hereditary hemorrhagic Gene Set

From 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 Set

From 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 neoplasms; intestinal polyposis Gene Set

From 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.

adenomatous polyposis coli; colorectal neoplasms; intestinal polyps Gene Set

From 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.

intestinal polyposis Gene Set

From 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 Set

From 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.

large intestinal polyposis Gene Set

From 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 Set

From 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.

polyposis, juvenile intestinal Gene Set

From OMIM Gene-Disease Associations

genes associated with the polyposis, juvenile intestinal phenotype from the curated OMIM Gene-Disease Associations dataset.

Intestinal Polyposis Gene Set

From 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.

Polyposis, Adenomatous Intestinal Gene Set

From 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.

Large Intestinal Polyposis Gene Set

From 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.

Familial multiple polyposis syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial multiple polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

familial adenomatous polyposis Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease familial adenomatous polyposis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

familial adenomatous polyposis Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial adenomatous polyposis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial adenomatous polyposis. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial adenomatous polyposis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

late onset of familial adenomatous polyposis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease late onset of familial adenomatous polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial adenomatous polyposis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial adenomatous polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

late onset familial adenomatous polyposis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease late onset familial adenomatous polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Familial Adenomatous Polyposis Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Familial Adenomatous Polyposis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Familial Adenomatous Polyposis Gene Set

From 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 Set

From 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 Set

From 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 3 Gene Set

From 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 Set

From 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 Set

From 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.

Familial adenomatous polyposis Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Familial adenomatous polyposis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Classic or attenuated familial adenomatous polyposis Gene Set

From 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.

Familial multiple polyposis syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Familial multiple polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

AXIN2-related attenuated familial adenomatous polyposis Gene Set

From 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 Set

From 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 Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Attenuated familial adenomatous polyposis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

constriction, pathologic; crohn disease; crohn's disease; intestinal fistula; intestinal obstruction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease constriction, pathologic; crohn disease; crohn's disease; intestinal fistula; intestinal obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From CTD Gene-Disease Associations

genes/proteins associated with the disease THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN from the curated CTD Gene-Disease Associations dataset.

amyloidosis, familial; familial mediterranean fever Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyloidosis, familial; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

albuminuria; amyloidosis, familial; familial mediterranean fever Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; amyloidosis, familial; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple familial trichoepithelioma and familial cylindromatosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple familial trichoepithelioma and familial cylindromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amyloidosis, familial; familial mediterranean fever; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyloidosis, familial; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial hemiplegic migraine and benign familial infantile convulsions Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial hemiplegic migraine and benign familial infantile convulsions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Adenomatous polyposis coli:Gardner syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Adenomatous polyposis coli:Gardner syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Juvenile polyposis syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Juvenile polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MYH-associated polyposis Gene Set

From 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 Set

From ClinVar Gene-Phenotype Associations

genes associated with the Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Adenomatous polyposis coli Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Adenomatous polyposis coli phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polyposis Syndrome, Hereditary Mixed, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polyposis Syndrome, Hereditary Mixed, 2 from the curated CTD Gene-Disease Associations dataset.

Colorectal Adenomatous Polyposis, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Colorectal Adenomatous Polyposis, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Juvenile Polyposis with Hereditary Hemorrhagic Telangiectasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Juvenile Polyposis with Hereditary Hemorrhagic Telangiectasia from the curated CTD Gene-Disease Associations dataset.

Adenomatous Polyposis Coli Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Adenomatous Polyposis Coli from the curated CTD Gene-Disease Associations dataset.

Juvenile polyposis syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Juvenile polyposis syndrome from the curated CTD Gene-Disease Associations dataset.

adenomatous polyposis coli; syndrome Gene Set

From 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.

nasal polyposis Gene Set

From 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 Set

From 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.

adenocarcinoma; adenomatous polyposis coli Gene Set

From 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 Set

From 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.

colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate Gene Set

From 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.

adenomatous polyposis coli; duodenal neoplasms Gene Set

From 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; adenomatous polyps Gene Set

From 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.

adenomatous polyposis coli; colorectal neoplasms; neoplasm recurrence, local Gene Set

From 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.

juvenile polyposis Gene Set

From 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.

adenomatous polyposis coli Gene Set

From 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 Set

From 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.

hereditary non-polyposis colon cancer. Gene Set

From 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 Set

From 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.

adenomatous polyposis coli; colonic neoplasms; rectal neoplasms Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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; bone neoplasms; epidermal cyst; gardner syndrome; gardner's syndrome; osteoma Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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.

polyposis Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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.

adenomatous colonic polyposis Gene Set

From 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.

hyperplastic colonic polyposis Gene Set

From 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 Set

From 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.

Adenomatous Polyposis Coli Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Adenomatous polyposis coli protein domain from the InterPro Predicted Protein Domain Annotations dataset.

juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

brain tumor-polyposis syndrome 2 Gene Set

From 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 Set

From OMIM Gene-Disease Associations

genes associated with the polyposis syndrome, hereditary mixed, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

adenomatous polyposis coli Gene Set

From 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 Set

From OMIM Gene-Disease Associations

genes associated with the colorectal adenomatous polyposis, autosomal recessive, with pilomatricomas phenotype from the curated OMIM Gene-Disease Associations dataset.

juvenile polyposis syndrome, infantile form Gene Set

From OMIM Gene-Disease Associations

genes associated with the juvenile polyposis syndrome, infantile form phenotype from the curated OMIM Gene-Disease Associations dataset.

Adenomatous Polyposis Coli Gene Set

From 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.

Mutyh-Associate Polyposis Gene Set

From 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.

Juvenile Polyposis Syndrome Gene Set

From 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.

Adenomatous Polyposis Coli With Congenital Cholesteatoma Gene Set

From 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.

Brain Tumor-Polyposis Syndrome 2 (Disorder) Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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.

Juvenile Gastrointestinal Polyposis Gene Set

From 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 Set

From 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.

Colorectal Adenomatous Polyposis, Autosomal Recessive Gene Set

From 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.

Colon Serrated Polyposis Gene Set

From 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 Set

From 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.

Adenomatous Colonic Polyposis Gene Set

From 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.

Juvenile polyposis syndrome Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Brain tumor-polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Adenomatous polyposis coli Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Adenomatous polyposis coli phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Duodenal polyposis Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Duodenal polyposis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Adenomatous colonic polyposis Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Adenomatous colonic polyposis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Hyperplastic colonic polyposis Gene Set

From 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 Set

From 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 Set

From 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.

Colorectal adenomatous polyposis Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Colorectal adenomatous polyposis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Juvenile polyposis syndrome Gene Set

From 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 Set

From 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 Set

From 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 Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Juvenile polyposis of stomach phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Polymerase proofreading-related adenomatous polyposis Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Polymerase proofreading-related adenomatous polyposis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Gastric adenocarcinoma and proximal polyposis of the stomach Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Bronchiectasis and nasal polyposis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

CTNNB1-24651522-LGR5+ INTESTINAL STEM CELL-HUMAN Gene Set

From ChEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CTNNB1-24651522-LGR5+ INTESTINAL STEM CELL-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

HNF4A-19761587-HUMAN INTESTINAL CELL LINE CACO-2-human Gene Set

From ChEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the HNF4A-19761587-HUMAN INTESTINAL CELL LINE CACO-2-human transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

Hypomagnesemia 1, intestinal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypomagnesemia 1, intestinal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Intestinal pseudoobstruction neuronal chronic idiopathic X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Intestinal pseudoobstruction neuronal chronic idiopathic X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

vasoactive intestinal peptide, 4-chloro-Phe(6)-Leu(17)- Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical vasoactive intestinal peptide, 4-chloro-Phe(6)-Leu(17)- from the curated CTD Gene-Chemical Interactions dataset.

Intestinal Neoplasms Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Intestinal Neoplasms from the curated CTD Gene-Disease Associations dataset.

Hypomagnesemia 1, Intestinal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypomagnesemia 1, Intestinal from the curated CTD Gene-Disease Associations dataset.

Congenital idiopathic intestinal pseudoobstruction Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital idiopathic intestinal pseudoobstruction from the curated CTD Gene-Disease Associations dataset.

Carcinoid Tumors, Intestinal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Carcinoid Tumors, Intestinal from the curated CTD Gene-Disease Associations dataset.

Intestinal Obstruction Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Intestinal Obstruction from the curated CTD Gene-Disease Associations dataset.

Intestinal Diseases Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Intestinal Diseases from the curated CTD Gene-Disease Associations dataset.

Intestinal Perforation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Intestinal Perforation from the curated CTD Gene-Disease Associations dataset.

Megacystis microcolon intestinal hypoperistalsis syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Megacystis microcolon intestinal hypoperistalsis syndrome from the curated CTD Gene-Disease Associations dataset.

Intestinal Polyps Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Intestinal Polyps from the curated CTD Gene-Disease Associations dataset.

Intestinal Diseases Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Intestinal Diseases in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

intestinal pseudo-obstruction Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease intestinal pseudo-obstruction from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

intestinal obstruction Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease intestinal obstruction from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

intestinal disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease intestinal disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

intestinal cancer Gene Set

From DISEASES Experimental Gene-Disease Association Evidence Scores

genes associated with the disease intestinal cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

intestinal disease Gene Set

From DISEASES Experimental Gene-Disease Association Evidence Scores

genes associated with the disease intestinal disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

intestinal atresia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease intestinal atresia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

multiple intestinal atresia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease multiple intestinal atresia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

intestinal schistosomiasis Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease intestinal schistosomiasis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

intestinal botulism Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease intestinal botulism in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

intestinal neuroendocrine benign tumor Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease intestinal neuroendocrine benign tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

intestinal disaccharidase deficiency Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease intestinal disaccharidase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

chronic intestinal vascular insufficiency Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease chronic intestinal vascular insufficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

intestinal cancer Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease intestinal cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

intestinal disease Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease intestinal disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

intestinal volvulus Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease intestinal volvulus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

intestinal impaction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease intestinal impaction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

intestinal obstruction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease intestinal obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

intestinal perforation Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease intestinal perforation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

intestinal benign neoplasm Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease intestinal benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

small intestinal sarcoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease small intestinal sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

intestinal tuberculosis Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease intestinal tuberculosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

intestinal pseudo-obstruction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease intestinal pseudo-obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

intestinal infectious disease Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease intestinal infectious disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

intestinal pseudo-obstruction; mitochondrial diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease intestinal pseudo-obstruction; mitochondrial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gastritis, chronic atrophic; metaplasia, intestinal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gastritis, chronic atrophic; metaplasia, intestinal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; intestinal neoplasms; lymphoma; lymphoma, b-cell, marginal zone Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; intestinal neoplasms; lymphoma; lymphoma, b-cell, marginal zone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis; colitis, ulcerative; crohn disease; crohn's disease; ileal diseases; intestinal fistula; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis; colitis, ulcerative; crohn disease; crohn's disease; ileal diseases; intestinal fistula; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

intestinal neuronal dysplasia type b (ind b) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease intestinal neuronal dysplasia type b (ind b) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; intestinal obstruction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; intestinal obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

helicobacter infections; intestinal neoplasms; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease helicobacter infections; intestinal neoplasms; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colorectal neoplasms; intestinal polyps Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal neoplasms; intestinal polyps in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

deafness; diabetes complications; diabetes mellitus; intestinal pseudo-obstruction; pancreatitis; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease deafness; diabetes complications; diabetes mellitus; intestinal pseudo-obstruction; pancreatitis; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

intestinal neoplasms; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease intestinal neoplasms; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

helicobacter infections; intestinal neoplasms; precancerous conditions; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease helicobacter infections; intestinal neoplasms; precancerous conditions; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; intestinal obstruction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; intestinal obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

intestinal neoplasms; lymphatic metastasis; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease intestinal neoplasms; lymphatic metastasis; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gastritis; intestinal metaplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gastritis; intestinal metaplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperinsulinemia; fat oxidation; intestinal fatty acid absorption Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperinsulinemia; fat oxidation; intestinal fatty acid absorption in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

intestinal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease intestinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; adenocarcinoma, mucinous; carcinoma, papillary; carcinoma, signet ring cell; intestinal neoplasms; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; adenocarcinoma, mucinous; carcinoma, papillary; carcinoma, signet ring cell; intestinal neoplasms; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ethmoid intestinal-type adenocarcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ethmoid intestinal-type adenocarcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gastritis, atrophic; helicobacter infections; intestinal diseases; metaplasia; precancerous conditions Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gastritis, atrophic; helicobacter infections; intestinal diseases; metaplasia; precancerous conditions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

helicobacter infections; intestinal diseases; metaplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease helicobacter infections; intestinal diseases; metaplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

intestinal Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term intestinal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

intestinal cholesterol absorption Gene Set

From GO Biological Process Annotations 2015

genes participating in the intestinal cholesterol absorption biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of intestinal cholesterol absorption Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of intestinal cholesterol absorption biological process from the curated GO Biological Process Annotations 2015 dataset.

intestinal epithelial cell migration Gene Set

From GO Biological Process Annotations 2015

genes participating in the intestinal epithelial cell migration biological process from the curated GO Biological Process Annotations 2015 dataset.

negative regulation of intestinal cholesterol absorption Gene Set

From GO Biological Process Annotations 2015

genes participating in the negative regulation of intestinal cholesterol absorption biological process from the curated GO Biological Process Annotations 2015 dataset.

gastro-intestinal system smooth muscle contraction Gene Set

From GO Biological Process Annotations 2015

genes participating in the gastro-intestinal system smooth muscle contraction biological process from the curated GO Biological Process Annotations 2015 dataset.

positive regulation of intestinal epithelial structure maintenance Gene Set

From GO Biological Process Annotations 2015

genes participating in the positive regulation of intestinal epithelial structure maintenance biological process from the curated GO Biological Process Annotations 2015 dataset.

intestinal epithelial structure maintenance Gene Set

From GO Biological Process Annotations 2015

genes participating in the intestinal epithelial structure maintenance biological process from the curated GO Biological Process Annotations 2015 dataset.

intestinal epithelial cell maturation Gene Set

From GO Biological Process Annotations 2015

genes participating in the intestinal epithelial cell maturation biological process from the curated GO Biological Process Annotations 2015 dataset.

negative regulation of intestinal phytosterol absorption Gene Set

From GO Biological Process Annotations 2015

genes participating in the negative regulation of intestinal phytosterol absorption biological process from the curated GO Biological Process Annotations 2015 dataset.

intestinal epithelial cell differentiation Gene Set

From GO Biological Process Annotations 2015

genes participating in the intestinal epithelial cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.

intestinal absorption Gene Set

From GO Biological Process Annotations 2015

genes participating in the intestinal absorption biological process from the curated GO Biological Process Annotations 2015 dataset.

intestinal epithelial cell development Gene Set

From GO Biological Process Annotations 2015

genes participating in the intestinal epithelial cell development biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of intestinal epithelial structure maintenance Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of intestinal epithelial structure maintenance biological process from the curated GO Biological Process Annotations 2015 dataset.

establishment of endothelial intestinal barrier Gene Set

From GO Biological Process Annotations 2015

genes participating in the establishment of endothelial intestinal barrier biological process from the curated GO Biological Process Annotations 2015 dataset.

vasoactive intestinal polypeptide receptor activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the vasoactive intestinal polypeptide receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

intestinal cancer Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease intestinal cancer in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

intestinal benign neoplasm Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease intestinal benign neoplasm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

intestinal disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease intestinal disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

intestinal carcinoid Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the intestinal carcinoid phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

intestinal obstruction Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the intestinal obstruction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

intestinal bleeding Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the intestinal bleeding phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

intestinal obstruction Gene Set

From HPO Gene-Disease Associations

genes associated with the intestinal obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

intestinal lymphangiectasia Gene Set

From HPO Gene-Disease Associations

genes associated with the intestinal lymphangiectasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

intestinal pseudo-obstruction Gene Set

From HPO Gene-Disease Associations

genes associated with the intestinal pseudo-obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

intestinal edema Gene Set

From HPO Gene-Disease Associations

genes associated with the intestinal edema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

intestinal bleeding Gene Set

From HPO Gene-Disease Associations

genes associated with the intestinal bleeding phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

intestinal carcinoid Gene Set

From HPO Gene-Disease Associations

genes associated with the intestinal carcinoid phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of small intestinal villus morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of small intestinal villus morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

intestinal atresia Gene Set

From HPO Gene-Disease Associations

genes associated with the intestinal atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

small intestinal stenosis Gene Set

From HPO Gene-Disease Associations

genes associated with the small intestinal stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

intestinal malrotation Gene Set

From HPO Gene-Disease Associations

genes associated with the intestinal malrotation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

intestinal polyp Gene Set

From HPO Gene-Disease Associations

genes associated with the intestinal polyp phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

intestinal fistula Gene Set

From HPO Gene-Disease Associations

genes associated with the intestinal fistula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

intestinal hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the intestinal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Intestinal Neoplasms Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Intestinal Neoplasms phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Intestinal Fistula Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Intestinal Fistula phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Intestinal Obstruction Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Intestinal Obstruction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Intestinal Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Intestinal Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Intestinal Pseudo-Obstruction Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Intestinal Pseudo-Obstruction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Intestinal Atresia Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Intestinal Atresia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Intestinal Polyps Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Intestinal Polyps phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

GPCR, family 2, vasoactive intestinal peptide receptor 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the GPCR, family 2, vasoactive intestinal peptide receptor 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

GPCR, family 2, vasoactive intestinal peptide receptor 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the GPCR, family 2, vasoactive intestinal peptide receptor 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

GPCR, family 2, vasoactive intestinal peptide receptor Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the GPCR, family 2, vasoactive intestinal peptide receptor protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Vasoactive intestinal peptide Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Vasoactive intestinal peptide protein domain from the InterPro Predicted Protein Domain Annotations dataset.

intestinal/bowel diverticulum Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the intestinal/bowel diverticulum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal intestinal mucosa morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal intestinal mucosa morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased small intestinal microvillus size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased small intestinal microvillus size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

intestinal hypoperistalsis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the intestinal hypoperistalsis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased intestinal cholesterol absorption Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased intestinal cholesterol absorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal intestinal transit time Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal intestinal transit time phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased intestinal cholesterol absorption Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased intestinal cholesterol absorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal intestinal mineral absorption Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal intestinal mineral absorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

intestinal ulcer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the intestinal ulcer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

intestinal inflammation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the intestinal inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased small intestinal villus size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased small intestinal villus size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

intestinal edema Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the intestinal edema phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

remittent intestinal hemorrhage Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the remittent intestinal hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal small intestinal crypt cell proliferation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal small intestinal crypt cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal intestinal smooth muscle morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal intestinal smooth muscle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

intestinal obstruction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the intestinal obstruction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal intestinal peristalsis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal intestinal peristalsis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal intestinal absorption Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal intestinal absorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal intestinal cholesterol absorption Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal intestinal cholesterol absorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal intestinal enteroendocrine cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal intestinal enteroendocrine cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal intestinal lipid absorption Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal intestinal lipid absorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased intestinal adenocarcinoma incidence Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased intestinal adenocarcinoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

large intestinal inflammation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the large intestinal inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal intestinal secretion Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal intestinal secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal small intestinal crypt cell physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal small intestinal crypt cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal small intestinal microvillus morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal small intestinal microvillus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal intestinal epithelium morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal intestinal epithelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal intestinal calcium absorption Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal intestinal calcium absorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal small intestinal transit time Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal small intestinal transit time phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

small intestinal prolapse Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the small intestinal prolapse phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal intestinal iron level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal intestinal iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased intestinal calcium absorption Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased intestinal calcium absorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired contractility of intestinal smooth muscle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired contractility of intestinal smooth muscle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal small intestinal villus morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal small intestinal villus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased small intestinal crypt cell apoptosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased small intestinal crypt cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal large intestinal transit time Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal large intestinal transit time phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased intestinal adenoma incidence Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased intestinal adenoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

small intestinal inflammation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the small intestinal inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal intestinal goblet cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal intestinal goblet cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

intestinal atresia, multiple Gene Set

From OMIM Gene-Disease Associations

genes associated with the intestinal atresia, multiple phenotype from the curated OMIM Gene-Disease Associations dataset.

carcinoid tumors, intestinal Gene Set

From OMIM Gene-Disease Associations

genes associated with the carcinoid tumors, intestinal phenotype from the curated OMIM Gene-Disease Associations dataset.

hypomagnesemia 1, intestinal Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypomagnesemia 1, intestinal phenotype from the curated OMIM Gene-Disease Associations dataset.

hydrocephalus with congenital idiopathic intestinal pseudoobstruction Gene Set

From OMIM Gene-Disease Associations

genes associated with the hydrocephalus with congenital idiopathic intestinal pseudoobstruction phenotype from the curated OMIM Gene-Disease Associations dataset.

intestinal pseudoobstruction, neuronal Gene Set

From OMIM Gene-Disease Associations

genes associated with the intestinal pseudoobstruction, neuronal phenotype from the curated OMIM Gene-Disease Associations dataset.

intestinal Gene Set

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term intestinal in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

intestinal mucosa Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue intestinal mucosa from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

intestinal epithelium Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue intestinal epithelium from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

intestinal muscle Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue intestinal muscle from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

intestinal mucosa Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue intestinal mucosa in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

intestinal cancer cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue intestinal cancer cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

intestinal muscle Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue intestinal muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

intestinal epithelium Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue intestinal epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

intestinal juice Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue intestinal juice in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

intestinal gland Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue intestinal gland in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

intestinal cancer cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue intestinal cancer cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

intestinal cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue intestinal cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

intestinal wall Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue intestinal wall in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

Large_Intestine-intestinal crypt stem cell Gene Set

From Tabula Sapiens Gene-Cell Associations

genes with high or low expression in Large_Intestine-intestinal crypt stem cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.

Large_Intestine-intestinal crypt stem cell of large intestine Gene Set

From Tabula Sapiens Gene-Cell Associations

genes with high or low expression in Large_Intestine-intestinal crypt stem cell of large intestine relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.

Large_Intestine-intestinal enteroendocrine cell Gene Set

From Tabula Sapiens Gene-Cell Associations

genes with high or low expression in Large_Intestine-intestinal enteroendocrine cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.

Large_Intestine-intestinal tuft cell Gene Set

From Tabula Sapiens Gene-Cell Associations

genes with high or low expression in Large_Intestine-intestinal tuft cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.

Small_Intestine-intestinal crypt stem cell Gene Set

From Tabula Sapiens Gene-Cell Associations

genes with high or low expression in Small_Intestine-intestinal crypt stem cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.

Small_Intestine-intestinal crypt stem cell of small intestine Gene Set

From Tabula Sapiens Gene-Cell Associations

genes with high or low expression in Small_Intestine-intestinal crypt stem cell of small intestine relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.

Small_Intestine-intestinal enteroendocrine cell Gene Set

From Tabula Sapiens Gene-Cell Associations

genes with high or low expression in Small_Intestine-intestinal enteroendocrine cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.

Small_Intestine-intestinal tuft cell Gene Set

From Tabula Sapiens Gene-Cell Associations

genes with high or low expression in Small_Intestine-intestinal tuft cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.

Intestinal Volvulus Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intestinal Volvulus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intestinal T-Cell Lymphoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intestinal T-Cell Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Gastric Cancer, Intestinal Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Gastric Cancer, Intestinal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intestinal Angioedema Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intestinal Angioedema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Neuronal Intestinal Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Neuronal Intestinal Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intestinal Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intestinal Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Chronic Intestinal Pseudo-Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Chronic Intestinal Pseudo-Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intestinal Metaplasia Of Gastric Mucosa Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intestinal Metaplasia Of Gastric Mucosa in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Megacystis Microcolon Intestinal Hypoperistalsis Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Megacystis Microcolon Intestinal Hypoperistalsis Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intestinal Pseudo-Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intestinal Pseudo-Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intestinal Cancer Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intestinal Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intestinal Perforation Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intestinal Perforation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Small Intestinal Bacterial Overgrowth Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Small Intestinal Bacterial Overgrowth in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intestinal Adenocarcinoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intestinal Adenocarcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intestinal Adenoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intestinal Adenoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intestinal Carcinoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intestinal Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Immunoproliferative Small Intestinal Disease Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Immunoproliferative Small Intestinal Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Esophageal Intestinal Metaplasia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Esophageal Intestinal Metaplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intestinal Neuroendocrine Tumor Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intestinal Neuroendocrine Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intestinal Graft Versus Host Disease Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intestinal Graft Versus Host Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intestinal-Type Sinonasal Adenocarcinoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intestinal-Type Sinonasal Adenocarcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Monomorphic Epitheliotropic Intestinal T-Cell Lymphoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Monomorphic Epitheliotropic Intestinal T-Cell Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Congenital Intestinal Aganglionosis Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Congenital Intestinal Aganglionosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Lymphangiectasis, Intestinal Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Lymphangiectasis, Intestinal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Small Intestinal Lymphoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Small Intestinal Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Small Intestinal Neuroendocrine Carcinoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Small Intestinal Neuroendocrine Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Primary Intestinal Lymphangiectasia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Primary Intestinal Lymphangiectasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Small Intestinal Neuroendocrine Neoplasm Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Small Intestinal Neuroendocrine Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intestinal Neuroendocrine Carcinoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intestinal Neuroendocrine Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Non-Intestinal Type Adenocarcinoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Non-Intestinal Type Adenocarcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Distal Intestinal Obstruction Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Distal Intestinal Obstruction Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Mucinous Adenocarcinoma, Intestinal Type Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Mucinous Adenocarcinoma, Intestinal Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Small Intestinal Neuroendocrine Tumor Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Small Intestinal Neuroendocrine Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intestinal Atresia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intestinal Atresia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intestinal Obstruction Co-Occurrent And Due To Decreased Peristalsis Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intestinal Obstruction Co-Occurrent And Due To Decreased Peristalsis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intestinal Necrosis Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intestinal Necrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Neonatal Intestinal Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Neonatal Intestinal Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Total Intestinal Aganglionosis Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Total Intestinal Aganglionosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intestinal Adenocarcinoma Of The Stomach Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intestinal Adenocarcinoma Of The Stomach in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intestinal Epithelial Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intestinal Epithelial Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intestinal Schistosomiasis Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intestinal Schistosomiasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Chronic Intestinal Failure Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Chronic Intestinal Failure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Congenital Idiopathic Intestinal Pseudoobstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Congenital Idiopathic Intestinal Pseudoobstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Neuronal Intestinal Pseudoobstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Neuronal Intestinal Pseudoobstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Acute Intestinal Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Acute Intestinal Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intestinal Microsporidiosis Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intestinal Microsporidiosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Small Intestinal Mucositis Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Small Intestinal Mucositis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intestinal Intraepithelial Neoplasia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intestinal Intraepithelial Neoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Childhood Small Intestinal Carcinoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Childhood Small Intestinal Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intestinal Carcinoid Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intestinal Carcinoid in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intestinal Infarction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intestinal Infarction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intestinal Nematode Infection Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intestinal Nematode Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Small Intestinal Sarcoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Small Intestinal Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Small Intestinal Infarction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Small Intestinal Infarction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Congenital Intestinal Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Congenital Intestinal Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Chronic Atrial And Intestinal Dysrhythmia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Chronic Atrial And Intestinal Dysrhythmia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intestinal Angiodysplasia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intestinal Angiodysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intestinal Metaplasia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Intestinal Metaplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Intestinal Malabsorption Of Fat Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Intestinal Malabsorption Of Fat in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Intestinal Fibrosis Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Intestinal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Intestinal Polyps Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Intestinal Polyps in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Intestinal Hemorrhage Nos Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Intestinal Hemorrhage Nos in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Intestinal Fistula Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Intestinal Fistula in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Functional Intestinal Obstruction Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Functional Intestinal Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Decreased Intestinal Transit Time Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Decreased Intestinal Transit Time in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Intestinal Hypoplasia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Intestinal Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Intestinal Edema Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Intestinal Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Decreased Small Intestinal Mucosa Lactase Activity Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Decreased Small Intestinal Mucosa Lactase Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

intestinal epithelial structure maintenance Gene Set

From GO Biological Process Annotations 2023

genes participating in the intestinal epithelial structure maintenance biological process from the curated GO Biological Process Annotations 2023 dataset.

intestinal stem cell homeostasis Gene Set

From GO Biological Process Annotations 2023

genes participating in the intestinal stem cell homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset.

intestinal cholesterol absorption Gene Set

From GO Biological Process Annotations 2023

genes participating in the intestinal cholesterol absorption biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of intestinal epithelial structure maintenance Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of intestinal epithelial structure maintenance biological process from the curated GO Biological Process Annotations 2023 dataset.

intestinal epithelial cell differentiation Gene Set

From GO Biological Process Annotations 2023

genes participating in the intestinal epithelial cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.

intestinal absorption Gene Set

From GO Biological Process Annotations 2023

genes participating in the intestinal absorption biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of intestinal absorption Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of intestinal absorption biological process from the curated GO Biological Process Annotations 2023 dataset.

intestinal lipid absorption Gene Set

From GO Biological Process Annotations 2023

genes participating in the intestinal lipid absorption biological process from the curated GO Biological Process Annotations 2023 dataset.

intestinal epithelial cell development Gene Set

From GO Biological Process Annotations 2023

genes participating in the intestinal epithelial cell development biological process from the curated GO Biological Process Annotations 2023 dataset.

intestinal D-glucose absorption Gene Set

From GO Biological Process Annotations 2023

genes participating in the intestinal D-glucose absorption biological process from the curated GO Biological Process Annotations 2023 dataset.

intestinal hexose absorption Gene Set

From GO Biological Process Annotations 2023

genes participating in the intestinal hexose absorption biological process from the curated GO Biological Process Annotations 2023 dataset.

host-mediated regulation of intestinal microbiota composition Gene Set

From GO Biological Process Annotations 2023

genes participating in the host-mediated regulation of intestinal microbiota composition biological process from the curated GO Biological Process Annotations 2023 dataset.

establishment of endothelial intestinal barrier Gene Set

From GO Biological Process Annotations 2023

genes participating in the establishment of endothelial intestinal barrier biological process from the curated GO Biological Process Annotations 2023 dataset.

negative regulation of intestinal absorption Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of intestinal absorption biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of intestinal epithelial structure maintenance Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of intestinal epithelial structure maintenance biological process from the curated GO Biological Process Annotations 2023 dataset.

large intestinal transit Gene Set

From GO Biological Process Annotations 2023

genes participating in the large intestinal transit biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of intestinal cholesterol absorption Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of intestinal cholesterol absorption biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of intestinal lipid absorption Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of intestinal lipid absorption biological process from the curated GO Biological Process Annotations 2023 dataset.

intestinal folate absorption Gene Set

From GO Biological Process Annotations 2023

genes participating in the intestinal folate absorption biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of intestinal lipid absorption Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of intestinal lipid absorption biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of gastro-intestinal system smooth muscle contraction Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of gastro-intestinal system smooth muscle contraction biological process from the curated GO Biological Process Annotations 2023 dataset.

negative regulation of intestinal phytosterol absorption Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of intestinal phytosterol absorption biological process from the curated GO Biological Process Annotations 2023 dataset.

negative regulation of intestinal cholesterol absorption Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of intestinal cholesterol absorption biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of intestinal cholesterol absorption Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of intestinal cholesterol absorption biological process from the curated GO Biological Process Annotations 2023 dataset.

intestinal epithelial cell migration Gene Set

From GO Biological Process Annotations 2023

genes participating in the intestinal epithelial cell migration biological process from the curated GO Biological Process Annotations 2023 dataset.

gastro-intestinal system smooth muscle contraction Gene Set

From GO Biological Process Annotations 2023

genes participating in the gastro-intestinal system smooth muscle contraction biological process from the curated GO Biological Process Annotations 2023 dataset.

intestinal motility Gene Set

From GO Biological Process Annotations 2023

genes participating in the intestinal motility biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of intestinal absorption Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of intestinal absorption biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of gastro-intestinal system smooth muscle contraction Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of gastro-intestinal system smooth muscle contraction biological process from the curated GO Biological Process Annotations 2023 dataset.

negative regulation of intestinal lipid absorption Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of intestinal lipid absorption biological process from the curated GO Biological Process Annotations 2023 dataset.

vasoactive intestinal polypeptide receptor activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the vasoactive intestinal polypeptide receptor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

CTNNB1-24651522-LGR5+-INTESTINAL-STEM-HUMAN Gene Set

From ChEA Transcription Factor Targets 2022

target genes of the CTNNB1-24651522-LGR5+-INTESTINAL-STEM-HUMAN transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.

CDX2-21402776-INTESTINAL-VILLUS-MOUSE Gene Set

From ChEA Transcription Factor Targets 2022

target genes of the CDX2-21402776-INTESTINAL-VILLUS-MOUSE transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.

remittent intestinal hemorrhage Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the remittent intestinal hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

small intestinal prolapse Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the small intestinal prolapse phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal intestinal mineral absorption Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal intestinal mineral absorption phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

decreased intestinal calcium absorption Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the decreased intestinal calcium absorption phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

intestinal obstruction Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the intestinal obstruction phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal intestinal mucosa morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal intestinal mucosa morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal intestinal enteroendocrine cell morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal intestinal enteroendocrine cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

intestinal hypoperistalsis Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the intestinal hypoperistalsis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

increased intestinal adenoma incidence Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the increased intestinal adenoma incidence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal intestinal epithelium morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal intestinal epithelium morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

increased intestinal adenocarcinoma incidence Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the increased intestinal adenocarcinoma incidence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

intestinal hemorrhage Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the intestinal hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal intestinal glucose absorption Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal intestinal glucose absorption phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal intestinal goblet cell morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal intestinal goblet cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal intestinal absorption Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal intestinal absorption phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

intestinal mucus accumulation Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the intestinal mucus accumulation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

decreased intestinal epithelial sodium ion transmembrane transport Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the decreased intestinal epithelial sodium ion transmembrane transport phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

decreased intestinal epithelial chloride transmembrane transport Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the decreased intestinal epithelial chloride transmembrane transport phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

intestinal ulcer Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the intestinal ulcer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal small intestinal crypt cell physiology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal small intestinal crypt cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

decreased small intestinal villus number Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the decreased small intestinal villus number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

intestinal edema Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the intestinal edema phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

intestinal inflammation Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the intestinal inflammation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

small intestinal inflammation Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the small intestinal inflammation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal intestinal peristalsis Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal intestinal peristalsis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

decreased intestinal cholesterol absorption Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the decreased intestinal cholesterol absorption phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

increased intestinal cholesterol absorption Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the increased intestinal cholesterol absorption phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal small intestinal villus morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal small intestinal villus morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

large intestinal inflammation Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the large intestinal inflammation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

increased intestinal iron level Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the increased intestinal iron level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal small intestinal microvillus morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal small intestinal microvillus morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal intestinal transit time Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal intestinal transit time phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

decreased small intestinal villus height Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the decreased small intestinal villus height phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal intestinal lipid absorption Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal intestinal lipid absorption phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal intestinal secretion Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal intestinal secretion phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

decreased small intestinal villus size Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the decreased small intestinal villus size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal intestinal smooth muscle morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal intestinal smooth muscle morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal small intestinal transit time Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal small intestinal transit time phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

decreased intestinal adenoma incidence Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the decreased intestinal adenoma incidence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

decreased intestinal glucose absorption Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the decreased intestinal glucose absorption phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

increased intestinal glucose absorption Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the increased intestinal glucose absorption phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

intestinal/bowel diverticulum Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the intestinal/bowel diverticulum phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal large intestinal transit time Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal large intestinal transit time phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal small intestinal crypt cell proliferation Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal small intestinal crypt cell proliferation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

branched small intestinal villi Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the branched small intestinal villi phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

decreased small intestinal microvillus size Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the decreased small intestinal microvillus size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

increased small intestinal crypt cell apoptosis Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the increased small intestinal crypt cell apoptosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal intestinal fructose absorption Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal intestinal fructose absorption phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

small intestinal villus atrophy Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the small intestinal villus atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal intestinal epithelium physiology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal intestinal epithelium physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

fused small intestinal villi Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the fused small intestinal villi phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal intestinal goblet cell physiology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal intestinal goblet cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

blunted small intestinal villi Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the blunted small intestinal villi phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

decreased intestinal iron level Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the decreased intestinal iron level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

intestinal stenosis Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the intestinal stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

intestinal fibrosis Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the intestinal fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal intestinal cholesterol absorption Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal intestinal cholesterol absorption phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

decreased intestinal mucosa thickness Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the decreased intestinal mucosa thickness phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal intestinal villus goblet cell morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal intestinal villus goblet cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal intestinal rotation Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal intestinal rotation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

clubbed small intestinal villi Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the clubbed small intestinal villi phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

Human - Fetal Development - L1 - Intestinal epithelial cells Gene Set

From HuBMAP Azimuth Cell Type Annotations

genes associated with the Human - Fetal Development - L1 - Intestinal epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.

Human - Fetal Development - L2 - Intestine-Intestinal epithelial cells Gene Set

From HuBMAP Azimuth Cell Type Annotations

genes associated with the Human - Fetal Development - L2 - Intestine-Intestinal epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.

Intestinal cell_Biliary tract_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Intestinal cell_Biliary tract_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Intestinal stem cell_Colon_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Intestinal stem cell_Colon_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Intestinal stem cell_Esophagus_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Intestinal stem cell_Esophagus_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Intestinal stem cell_Gastrointestinal tract_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Intestinal stem cell_Gastrointestinal tract_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Intestinal epithelial cell_Stomach_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Intestinal epithelial cell_Stomach_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Intestinal stem cell_Small intestine_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Intestinal stem cell_Small intestine_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Small intestinal stem cell_Small intestine_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Small intestinal stem cell_Small intestine_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Intestinal stem cell_Small intestine_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Intestinal stem cell_Small intestine_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Intestinal stem cell_Intestine_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Intestinal stem cell_Intestine_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Quiescent small intestinal stem cell_Small intestine_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Quiescent small intestinal stem cell_Small intestine_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Intestinal epithelial stem cell_Intestine_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Intestinal epithelial stem cell_Intestine_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Intestinal stem cell_Colon epithelium_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Intestinal stem cell_Colon epithelium_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Intestinal epithelial stem cell_Intestine_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Intestinal epithelial stem cell_Intestine_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Intestinal epithelial stem cell_Jejunum_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Intestinal epithelial stem cell_Jejunum_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Intestinal stem cell_Intestinal crypt_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Intestinal stem cell_Intestinal crypt_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Eosinophil_Small intestinal crypt_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Eosinophil_Small intestinal crypt_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Enterochromaffin cell_Small intestinal crypt_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Enterochromaffin cell_Small intestinal crypt_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Epithelial stem cell_Small intestinal crypt_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Epithelial stem cell_Small intestinal crypt_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Intestinal cell_Intestine_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Intestinal cell_Intestine_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Intestinal epithelial cell_Intestine_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Intestinal epithelial cell_Intestine_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Intestinal stem cell_Gut_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Intestinal stem cell_Gut_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Intestinal cell_Gut_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Intestinal cell_Gut_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Intestinal stem cell_Intestinal crypt_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Intestinal stem cell_Intestinal crypt_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Intestinal stem cell_Epithelium_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Intestinal stem cell_Epithelium_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Intestinal stem cell_Duodenum_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Intestinal stem cell_Duodenum_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Intestinal cell_Epithelium_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Intestinal cell_Epithelium_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Mature intestinal tuft cell_Intestine_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Mature intestinal tuft cell_Intestine_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Stem cell_Small intestinal crypt_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Stem cell_Small intestinal crypt_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Migratory cell_Small intestinal crypt_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Migratory cell_Small intestinal crypt_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Intestinal stem cell_Intestine_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Intestinal stem cell_Intestine_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Intestinal stem cell_Colon epithelium_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Intestinal stem cell_Colon epithelium_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Intestinal stem cell_PeriBiliary cell gland_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Intestinal stem cell_PeriBiliary cell gland_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Intestinal stem cell_Stomach_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Intestinal stem cell_Stomach_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Intestinal metaplasia cell_Stomach_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Intestinal metaplasia cell_Stomach_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Intestinal gastric cancer cell_Stomach_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Intestinal gastric cancer cell_Stomach_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Intestinal stem cell (ISC)_Undefined_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Intestinal stem cell (ISC)_Undefined_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Control of immune tolerance by vasoactive intestinal peptide Gene Set

From WikiPathways Pathways 2024

proteins participating in the Control of immune tolerance by vasoactive intestinal peptide pathway from the WikiPathways Pathways 2024 dataset.

Effect of intestinal microbiome on anticoagulant response of vitamin K antagonists Gene Set

From WikiPathways Pathways 2024

proteins participating in the Effect of intestinal microbiome on anticoagulant response of vitamin K antagonists pathway from the WikiPathways Pathways 2024 dataset.

Intestinal absorption Gene Set

From Reactome Pathways 2024

proteins participating in the Intestinal absorption pathway from the Reactome Pathways 2024 dataset.

Intestinal hexose absorption Gene Set

From Reactome Pathways 2024

proteins participating in the Intestinal hexose absorption pathway from the Reactome Pathways 2024 dataset.

Intestinal infectious diseases Gene Set

From Reactome Pathways 2024

proteins participating in the Intestinal infectious diseases pathway from the Reactome Pathways 2024 dataset.

Intestinal lipid absorption Gene Set

From Reactome Pathways 2024

proteins participating in the Intestinal lipid absorption pathway from the Reactome Pathways 2024 dataset.

Intestinal saccharidase deficiencies Gene Set

From Reactome Pathways 2024

proteins participating in the Intestinal saccharidase deficiencies pathway from the Reactome Pathways 2024 dataset.

intestinal epithelial structure maintenance Gene Set

From GO Biological Process Annotations 2025

genes participating in the intestinal epithelial structure maintenance biological process from the curated GO Biological Process Annotations 2025 dataset.

intestinal stem cell homeostasis Gene Set

From GO Biological Process Annotations 2025

genes participating in the intestinal stem cell homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset.

intestinal cholesterol absorption Gene Set

From GO Biological Process Annotations 2025

genes participating in the intestinal cholesterol absorption biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of intestinal epithelial structure maintenance Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of intestinal epithelial structure maintenance biological process from the curated GO Biological Process Annotations 2025 dataset.

intestinal epithelial cell differentiation Gene Set

From GO Biological Process Annotations 2025

genes participating in the intestinal epithelial cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.

intestinal absorption Gene Set

From GO Biological Process Annotations 2025

genes participating in the intestinal absorption biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of intestinal absorption Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of intestinal absorption biological process from the curated GO Biological Process Annotations 2025 dataset.

intestinal lipid absorption Gene Set

From GO Biological Process Annotations 2025

genes participating in the intestinal lipid absorption biological process from the curated GO Biological Process Annotations 2025 dataset.

intestinal epithelial cell development Gene Set

From GO Biological Process Annotations 2025

genes participating in the intestinal epithelial cell development biological process from the curated GO Biological Process Annotations 2025 dataset.

intestinal D-glucose absorption Gene Set

From GO Biological Process Annotations 2025

genes participating in the intestinal D-glucose absorption biological process from the curated GO Biological Process Annotations 2025 dataset.

intestinal hexose absorption Gene Set

From GO Biological Process Annotations 2025

genes participating in the intestinal hexose absorption biological process from the curated GO Biological Process Annotations 2025 dataset.

host-mediated regulation of intestinal microbiota composition Gene Set

From GO Biological Process Annotations 2025

genes participating in the host-mediated regulation of intestinal microbiota composition biological process from the curated GO Biological Process Annotations 2025 dataset.

establishment of endothelial intestinal barrier Gene Set

From GO Biological Process Annotations 2025

genes participating in the establishment of endothelial intestinal barrier biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of intestinal D-glucose absorption Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of intestinal D-glucose absorption biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of intestinal lipid absorption Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of intestinal lipid absorption biological process from the curated GO Biological Process Annotations 2025 dataset.

negative regulation of intestinal absorption Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of intestinal absorption biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of intestinal epithelial structure maintenance Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of intestinal epithelial structure maintenance biological process from the curated GO Biological Process Annotations 2025 dataset.

large intestinal transit Gene Set

From GO Biological Process Annotations 2025

genes participating in the large intestinal transit biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of intestinal cholesterol absorption Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of intestinal cholesterol absorption biological process from the curated GO Biological Process Annotations 2025 dataset.

intestinal folate absorption Gene Set

From GO Biological Process Annotations 2025

genes participating in the intestinal folate absorption biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of intestinal lipid absorption Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of intestinal lipid absorption biological process from the curated GO Biological Process Annotations 2025 dataset.

intestinal iron absorption Gene Set

From GO Biological Process Annotations 2025

genes participating in the intestinal iron absorption biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of gastro-intestinal system smooth muscle contraction Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of gastro-intestinal system smooth muscle contraction biological process from the curated GO Biological Process Annotations 2025 dataset.

negative regulation of intestinal phytosterol absorption Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of intestinal phytosterol absorption biological process from the curated GO Biological Process Annotations 2025 dataset.

negative regulation of intestinal cholesterol absorption Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of intestinal cholesterol absorption biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of intestinal epithelial cell development Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of intestinal epithelial cell development biological process from the curated GO Biological Process Annotations 2025 dataset.

intestinal epithelial cell migration Gene Set

From GO Biological Process Annotations 2025

genes participating in the intestinal epithelial cell migration biological process from the curated GO Biological Process Annotations 2025 dataset.

gastro-intestinal system smooth muscle contraction Gene Set

From GO Biological Process Annotations 2025

genes participating in the gastro-intestinal system smooth muscle contraction biological process from the curated GO Biological Process Annotations 2025 dataset.

intestinal motility Gene Set

From GO Biological Process Annotations 2025

genes participating in the intestinal motility biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of intestinal cholesterol absorption Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of intestinal cholesterol absorption biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of intestinal absorption Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of intestinal absorption biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of gastro-intestinal system smooth muscle contraction Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of gastro-intestinal system smooth muscle contraction biological process from the curated GO Biological Process Annotations 2025 dataset.

negative regulation of intestinal lipid absorption Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of intestinal lipid absorption biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of intestinal epithelial cell development Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of intestinal epithelial cell development biological process from the curated GO Biological Process Annotations 2025 dataset.

type 1 vasoactive intestinal polypeptide receptor binding Gene Set

From GO Molecular Function Annotations 2025

genes performing the type 1 vasoactive intestinal polypeptide receptor binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.

type 2 vasoactive intestinal polypeptide receptor binding Gene Set

From GO Molecular Function Annotations 2025

genes performing the type 2 vasoactive intestinal polypeptide receptor binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.

vasoactive intestinal polypeptide receptor activity Gene Set

From GO Molecular Function Annotations 2025

genes performing the vasoactive intestinal polypeptide receptor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

vasoactive intestinal polypeptide receptor binding Gene Set

From GO Molecular Function Annotations 2025

genes performing the vasoactive intestinal polypeptide receptor binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.

Intestinal disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Intestinal disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Intestinal pseudo-obstruction Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Intestinal pseudo-obstruction from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

megacystis-microcolon-intestinal hypoperistalsis syndrome Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease megacystis-microcolon-intestinal hypoperistalsis syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Chronic atrial and intestinal dysrhythmia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Chronic atrial and intestinal dysrhythmia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Intestinal disease Gene Set

From DISEASES Experimental Gene-Disease Association Evidence Scores 2025

genes associated with the disease Intestinal disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.

Intestinal benign neoplasm Gene Set

From DISEASES Experimental Gene-Disease Association Evidence Scores 2025

genes associated with the disease Intestinal benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.

Intestinal obstruction Gene Set

From DISEASES Experimental Gene-Disease Association Evidence Scores 2025

genes associated with the disease Intestinal obstruction in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.

Intestinal cancer Gene Set

From DISEASES Experimental Gene-Disease Association Evidence Scores 2025

genes associated with the disease Intestinal cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.

Intestinal cancer Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Intestinal cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Intestinal disease Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Intestinal disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Intestinal benign neoplasm Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Intestinal benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Intestinal obstruction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Intestinal obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Intestinal infectious disease Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Intestinal infectious disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Intestinal volvulus Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Intestinal volvulus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple intestinal atresia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple intestinal atresia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Intestinal atresia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Intestinal atresia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Intestinal perforation Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Intestinal perforation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Intestinal pseudo-obstruction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Intestinal pseudo-obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Intestinal impaction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Intestinal impaction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

megacystis-microcolon-intestinal hypoperistalsis syndrome Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease megacystis-microcolon-intestinal hypoperistalsis syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Intestinal tuberculosis Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Intestinal tuberculosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Intestinal schistosomiasis Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Intestinal schistosomiasis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Chronic atrial and intestinal dysrhythmia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Chronic atrial and intestinal dysrhythmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Chronic intestinal vascular insufficiency Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Chronic intestinal vascular insufficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Intestinal botulism Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Intestinal botulism in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Pancreatic vasoactive intestinal peptide producing tumor Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Pancreatic vasoactive intestinal peptide producing tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Intestinal disaccharidase deficiency Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Intestinal disaccharidase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Intestinal hypomagnesemia 1 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Intestinal hypomagnesemia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Small intestinal sarcoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Small intestinal sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Neuronal intestinal dysplasia type B Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Neuronal intestinal dysplasia type B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Perinatal intestinal perforation Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Perinatal intestinal perforation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

X-linked chronic idiopathic intestinal pseudo-obstruction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease X-linked chronic idiopathic intestinal pseudo-obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Intestinal mucosa Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores 2025

proteins highly expressed in the tissue Intestinal mucosa from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.

Intestinal epithelium Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores 2025

proteins highly expressed in the tissue Intestinal epithelium from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.

Intestinal muscle Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores 2025

proteins highly expressed in the tissue Intestinal muscle from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.

Intestinal epithelium Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Intestinal epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Intestinal cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Intestinal cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Intestinal mucosa Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Intestinal mucosa in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Intestinal epithelial cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Intestinal epithelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Intestinal wall Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Intestinal wall in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Intestinal cancer cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Intestinal cancer cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Intestinal cancer cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Intestinal cancer cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Intestinal muscle Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Intestinal muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Intestinal juice Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Intestinal juice in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Intestinal gland Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Intestinal gland in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Intestinal polyp Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Intestinal polyp phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Intestinal hypomagnesemia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Intestinal hypomagnesemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Megacystis-microcolon-intestinal hypoperistalsis syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Megacystis-microcolon-intestinal hypoperistalsis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Intestinal pseudo-obstruction Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Intestinal pseudo-obstruction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Intestinal obstruction Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Intestinal obstruction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Hypoplastic pancreas-intestinal atresia-hypoplastic gallbalder syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Hypoplastic pancreas-intestinal atresia-hypoplastic gallbalder syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Chronic intestinal pseudoobstruction Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Chronic intestinal pseudoobstruction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Chronic atrial and intestinal dysrhythmia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Chronic atrial and intestinal dysrhythmia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Intestinal duplication Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Intestinal duplication phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Nonpersistence of intestinal lactase Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Nonpersistence of intestinal lactase phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Intestinal pseudoobstruction Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Intestinal pseudoobstruction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Intestinal permeability measurement Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Intestinal permeability measurement phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Intestinal immune network for IgA production Gene Set

From KEGG Pathways 2026

proteins participating in the Intestinal immune network for IgA production pathway from the KEGG Pathways 2026 dataset.

VASOACTIVE INTESTINAL PEPTIDE Gene Set

From DGIdb Drug Targets 2026

interacting proteins for the VASOACTIVE INTESTINAL PEPTIDE drug from theDGIdb Drug Targets 2026 dataset.

Familial Mediterranean fever Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial Mediterranean fever phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombocytosis, benign familial microcytic Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombocytosis, benign familial microcytic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Benign familial neonatal-infantile seizures Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Benign familial neonatal-infantile seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neurofibromatosis, familial spinal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neurofibromatosis, familial spinal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tumoral calcinosis, familial, hyperphosphatemic Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Tumoral calcinosis, familial, hyperphosphatemic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Febrile seizures, familial, 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Febrile seizures, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial restrictive cardiomyopathy 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial restrictive cardiomyopathy 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gaze palsy, familial horizontal, with progressive scoliosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gaze palsy, familial horizontal, with progressive scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hemiplegic migraine type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hemiplegic migraine type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hemiplegic migraine type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hemiplegic migraine type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hemiplegic migraine type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hemiplegic migraine type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Erythrocytosis, familial, 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Erythrocytosis, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Erythrocytosis, familial, 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Erythrocytosis, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Erythrocytosis, familial, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Erythrocytosis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aortic aneurysm, familial thoracic 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aortic aneurysm, familial thoracic 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial X-linked hypophosphatemic vitamin D refractory rickets Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial X-linked hypophosphatemic vitamin D refractory rickets phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infantile convulsions and paroxysmal choreoathetosis, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile convulsions and paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Benign familial neonatal seizures 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Benign familial neonatal seizures 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Benign familial neonatal seizures 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Benign familial neonatal seizures 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperuricemic nephropathy, familial juvenile, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperuricemic nephropathy, familial juvenile, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial cancer of breast Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial cancer of breast phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial benign pemphigus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial benign pemphigus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Episodic pain syndrome, familial, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Episodic pain syndrome, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperpigmentation, familial progressive, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperpigmentation, familial progressive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial aortopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial aortopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Digital arthropathy-brachydactyly, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Digital arthropathy-brachydactyly, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Episodic pain syndrome, familial, 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Episodic pain syndrome, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular dysplasia, familial, 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Febrile seizures, familial, 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Febrile seizures, familial, 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial benign hypercalcemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial benign hypercalcemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial fibrillation, familial, 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial fibrillation, familial, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial visceral amyloidosis, Ostertag type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial visceral amyloidosis, Ostertag type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dementia familial British Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dementia familial British phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial porencephaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial porencephaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 17 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 15 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypocalciuric hypercalcemia, familial, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypocalciuric hypercalcemia, familial, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

familial hyperinsulinism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the familial hyperinsulinism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperinsulinemic hypoglycemia familial 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperinsulinemic hypoglycemia familial 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Febrile seizures, familial, 3b Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Febrile seizures, familial, 3b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Paroxysmal familial ventricular fibrillation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Paroxysmal familial ventricular fibrillation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypercholesterolemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypercholesterolemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hidradenitis suppurativa, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hidradenitis suppurativa, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dementia, familial Danish Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dementia, familial Danish phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Progressive familial intrahepatic cholestasis 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Progressive familial intrahepatic cholestasis 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Progressive familial intrahepatic cholestasis 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Progressive familial intrahepatic cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Benign familial hematuria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Benign familial hematuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Progressive familial heart block type 1A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Progressive familial heart block type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Progressive familial heart block type 1B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Progressive familial heart block type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial dysautonomia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial dysautonomia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial febrile seizures 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial febrile seizures 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fleck retina, familial benign Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fleck retina, familial benign phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked familial exudative vitreoretinopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked familial exudative vitreoretinopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial colorectal cancer Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial colorectal cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial porphyria cutanea tarda Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial porphyria cutanea tarda phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 20 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 20 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Progressive familial intrahepatic cholestasis 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Progressive familial intrahepatic cholestasis 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Advanced sleep phase syndrome, familial, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Advanced sleep phase syndrome, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myoclonus, familial cortical Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myoclonus, familial cortical phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Migraine, familial basilar Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Migraine, familial basilar phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Breast-ovarian cancer, familial 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Breast-ovarian cancer, familial 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypercholanemia, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypercholanemia, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bone marrow failure, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bone marrow failure, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aortic aneurysm, familial thoracic 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aortic aneurysm, familial thoracic 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Advanced sleep phase syndrome, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Advanced sleep phase syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Candidiasis, familial, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Candidiasis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Candidiasis, familial, 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Candidiasis, familial, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypokalemia-hypomagnesemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypokalemia-hypomagnesemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myasthenia, limb-girdle, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenia, limb-girdle, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial fibrillation, familial, 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial fibrillation, familial, 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial fibrillation, familial, 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial fibrillation, familial, 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial fibrillation, familial, 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial fibrillation, familial, 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial fibrillation, familial, 17 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial fibrillation, familial, 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial fibrillation, familial, 16 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial fibrillation, familial, 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial fibrillation, familial, 15 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial fibrillation, familial, 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemophagocytic lymphohistiocytosis, familial, 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemophagocytic lymphohistiocytosis, familial, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemophagocytic lymphohistiocytosis, familial, 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemophagocytic lymphohistiocytosis, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemophagocytic lymphohistiocytosis, familial, 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemophagocytic lymphohistiocytosis, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemophagocytic lymphohistiocytosis, familial, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemophagocytic lymphohistiocytosis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ventricular fibrillation, paroxysmal familial, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ventricular fibrillation, paroxysmal familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial platelet disorder with associated myeloid malignancy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial platelet disorder with associated myeloid malignancy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial erythrocytosis, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial erythrocytosis, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial medullary thyroid carcinoma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial medullary thyroid carcinoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperinsulinemic hypoglycemia, familial, 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperinsulinemic hypoglycemia, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aortic aneurysm, familial thoracic 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aortic aneurysm, familial thoracic 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aortic aneurysm, familial thoracic 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aortic aneurysm, familial thoracic 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aortic aneurysm, familial thoracic 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aortic aneurysm, familial thoracic 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperlipidemia, familial combined Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperlipidemia, familial combined phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial amyloid polyneuropathy, Iowa type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial amyloid polyneuropathy, Iowa type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial fibrillation, familial, 14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial fibrillation, familial, 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial encephalopathy with neuroserpin inclusion bodies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial encephalopathy with neuroserpin inclusion bodies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epilepsy, familial adult myoclonic, 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, familial adult myoclonic, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial myxoma, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial myxoma, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lipodystrophy, familial partial, type 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lipodystrophy, familial partial, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lipodystrophy, familial partial, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lipodystrophy, familial partial, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypocalciuric hypercalcemia, familial, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypocalciuric hypercalcemia, familial, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypocalciuric hypercalcemia, familial, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypocalciuric hypercalcemia, familial, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial juvenile gout Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial juvenile gout phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiomyopathy:Familial hypertrophic cardiomyopathy 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiomyopathy:Familial hypertrophic cardiomyopathy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypobetalipoproteinemia, familial, associated with apob32 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypobetalipoproteinemia, familial, associated with apob32 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Breast-ovarian cancer, familial 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Breast-ovarian cancer, familial 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial fibrillation, familial, 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial fibrillation, familial, 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary cancer-predisposing syndrome:Erythrocytosis, familial, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary cancer-predisposing syndrome:Erythrocytosis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Primary familial hypertrophic cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Primary familial hypertrophic cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial type 3 hyperlipoproteinemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial type 3 hyperlipoproteinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tumoral calcinosis, familial, normophosphatemic Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Tumoral calcinosis, familial, normophosphatemic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cd8 deficiency, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cd8 deficiency, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial infantile myasthenia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial infantile myasthenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked familial atypical mycobacteriosis, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked familial atypical mycobacteriosis, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperthyroxinemia, familial dysalbuminemic Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperthyroxinemia, familial dysalbuminemic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial type 5 hyperlipoproteinemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial type 5 hyperlipoproteinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cutaneous telangiectasia and cancer syndrome, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cutaneous telangiectasia and cancer syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial renal glucosuria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial renal glucosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial pulmonary capillary hemangiomatosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial pulmonary capillary hemangiomatosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypoalphalipoproteinemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypoalphalipoproteinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial renal hypouricemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial renal hypouricemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

HYPERALDOSTERONISM, FAMILIAL, TYPE III Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the HYPERALDOSTERONISM, FAMILIAL, TYPE III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myoclonic epilepsy, familial infantile Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myoclonic epilepsy, familial infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypoplastic, glomerulocystic kidney Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypoplastic, glomerulocystic kidney phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial cold urticaria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial cold urticaria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aortic Aneurysm, Familial Abdominal 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aortic Aneurysm, Familial Abdominal 2 from the curated CTD Gene-Disease Associations dataset.

Familial myelofibrosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial myelofibrosis from the curated CTD Gene-Disease Associations dataset.

Nephronophthisis, familial juvenile Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nephronophthisis, familial juvenile from the curated CTD Gene-Disease Associations dataset.

Eosinophilia, Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Eosinophilia, Familial from the curated CTD Gene-Disease Associations dataset.

Hyperlipidemia, Familial Combined Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperlipidemia, Familial Combined from the curated CTD Gene-Disease Associations dataset.

Platelet Disorder, Familial, with Associated Myeloid Malignancy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Platelet Disorder, Familial, with Associated Myeloid Malignancy from the curated CTD Gene-Disease Associations dataset.

Hyperinsulinemic hypoglycemia, familial, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperinsulinemic hypoglycemia, familial, 6 from the curated CTD Gene-Disease Associations dataset.

BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.

Pemphigus, Benign Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pemphigus, Benign Familial from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Restrictive, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 1 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 9 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 8 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 2 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 6 from the curated CTD Gene-Disease Associations dataset.

Amyloidosis, familial visceral Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amyloidosis, familial visceral from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Hypertrophic, Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Hypertrophic, Familial from the curated CTD Gene-Disease Associations dataset.

Gaze Palsy, Familial Horizontal, with Progressive Scoliosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gaze Palsy, Familial Horizontal, with Progressive Scoliosis from the curated CTD Gene-Disease Associations dataset.

Atrial Fibrillation, Familial, 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Fibrillation, Familial, 8 from the curated CTD Gene-Disease Associations dataset.

Atrial Fibrillation, Familial, 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Fibrillation, Familial, 7 from the curated CTD Gene-Disease Associations dataset.

Atrial Fibrillation, Familial, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Fibrillation, Familial, 6 from the curated CTD Gene-Disease Associations dataset.

Atrial Fibrillation, Familial, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Fibrillation, Familial, 4 from the curated CTD Gene-Disease Associations dataset.

Cholestasis, progressive familial intrahepatic 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 1 from the curated CTD Gene-Disease Associations dataset.

Cholestasis, progressive familial intrahepatic 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 2 from the curated CTD Gene-Disease Associations dataset.

Myasthenia, Familial Infantile, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myasthenia, Familial Infantile, 1 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 4 from the curated CTD Gene-Disease Associations dataset.

Aortic Aneurysm, Familial Abdominal 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aortic Aneurysm, Familial Abdominal 1 from the curated CTD Gene-Disease Associations dataset.

STUTTERING, FAMILIAL PERSISTENT, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease STUTTERING, FAMILIAL PERSISTENT, 1 from the curated CTD Gene-Disease Associations dataset.

Dementia, familial British Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dementia, familial British from the curated CTD Gene-Disease Associations dataset.

Candidiasis familial chronic mucocutaneous, autosomal recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Candidiasis familial chronic mucocutaneous, autosomal recessive from the curated CTD Gene-Disease Associations dataset.

Gliosis, Familial Progressive Subcortical Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gliosis, Familial Progressive Subcortical from the curated CTD Gene-Disease Associations dataset.

CD8 Deficiency, Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CD8 Deficiency, Familial from the curated CTD Gene-Disease Associations dataset.

Insomnia, Fatal Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Insomnia, Fatal Familial from the curated CTD Gene-Disease Associations dataset.

SEIZURES, BENIGN FAMILIAL NEONATAL, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL NEONATAL, 2 from the curated CTD Gene-Disease Associations dataset.

Familial HDL deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial HDL deficiency from the curated CTD Gene-Disease Associations dataset.

Familial dermographism Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial dermographism from the curated CTD Gene-Disease Associations dataset.

Candidiasis, Familial, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Candidiasis, Familial, 3 from the curated CTD Gene-Disease Associations dataset.

HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE from the curated CTD Gene-Disease Associations dataset.

Erythrocytosis, Familial, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Erythrocytosis, Familial, 3 from the curated CTD Gene-Disease Associations dataset.

Erythrocytosis, Familial, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Erythrocytosis, Familial, 2 from the curated CTD Gene-Disease Associations dataset.

Visceral Myopathy, Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Visceral Myopathy, Familial from the curated CTD Gene-Disease Associations dataset.

Hyperthyroidism, Familial Gestational Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperthyroidism, Familial Gestational from the curated CTD Gene-Disease Associations dataset.

Hematuria, Benign Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hematuria, Benign Familial from the curated CTD Gene-Disease Associations dataset.

SEIZURES, BENIGN FAMILIAL INFANTILE, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL INFANTILE, 2 from the curated CTD Gene-Disease Associations dataset.

Febrile Convulsions, Familial, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Febrile Convulsions, Familial, 2 from the curated CTD Gene-Disease Associations dataset.

Migraine, Familial Hemiplegic, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Migraine, Familial Hemiplegic, 3 from the curated CTD Gene-Disease Associations dataset.

FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1 from the curated CTD Gene-Disease Associations dataset.

Cancer, Familial, with In Vitro Radioresistance Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cancer, Familial, with In Vitro Radioresistance from the curated CTD Gene-Disease Associations dataset.

Febrile Convulsions, Familial, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Febrile Convulsions, Familial, 5 from the curated CTD Gene-Disease Associations dataset.

Hypoparathyroidism familial isolated Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypoparathyroidism familial isolated from the curated CTD Gene-Disease Associations dataset.

Tumoral Calcinosis, Hyperphosphatemic, Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Tumoral Calcinosis, Hyperphosphatemic, Familial from the curated CTD Gene-Disease Associations dataset.

Atrial Fibrillation, Familial, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Fibrillation, Familial, 3 from the curated CTD Gene-Disease Associations dataset.

Hidradenitis suppurativa, familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hidradenitis suppurativa, familial from the curated CTD Gene-Disease Associations dataset.

Dementia, familial Danish Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dementia, familial Danish from the curated CTD Gene-Disease Associations dataset.

Familial medullary thyroid carcinoma Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial medullary thyroid carcinoma from the curated CTD Gene-Disease Associations dataset.

Interstitial Pneumonitis, Desquamative, Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Interstitial Pneumonitis, Desquamative, Familial from the curated CTD Gene-Disease Associations dataset.

Hemophagocytic lymphohistiocytosis, familial, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hemophagocytic lymphohistiocytosis, familial, 4 from the curated CTD Gene-Disease Associations dataset.

Pseudohyperkalemia, Familial, 2, due to Red Cell Leak Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pseudohyperkalemia, Familial, 2, due to Red Cell Leak from the curated CTD Gene-Disease Associations dataset.

Cirrhosis, Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cirrhosis, Familial from the curated CTD Gene-Disease Associations dataset.

Familial encephalopathy with neuroserpin inclusion bodies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial encephalopathy with neuroserpin inclusion bodies from the curated CTD Gene-Disease Associations dataset.

Lipodystrophy, Familial Partial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lipodystrophy, Familial Partial from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Restrictive, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 3 from the curated CTD Gene-Disease Associations dataset.

Familial Mediterranean Fever, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial Mediterranean Fever, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Familial Hypophosphatemic Rickets Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial Hypophosphatemic Rickets from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 3 from the curated CTD Gene-Disease Associations dataset.

Keratoacanthoma familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Keratoacanthoma familial from the curated CTD Gene-Disease Associations dataset.

Hepatic Adenomas, Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hepatic Adenomas, Familial from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 10 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 13 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 13 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 15 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 15 from the curated CTD Gene-Disease Associations dataset.

Familial Wilms tumor 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial Wilms tumor 2 from the curated CTD Gene-Disease Associations dataset.

Candidiasis, Familial, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Candidiasis, Familial, 1 from the curated CTD Gene-Disease Associations dataset.

Febrile Convulsions, Familial, 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Febrile Convulsions, Familial, 9 from the curated CTD Gene-Disease Associations dataset.

Hyperinsulinemic Hypoglycemia, Familial, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperinsulinemic Hypoglycemia, Familial, 4 from the curated CTD Gene-Disease Associations dataset.

Hyperinsulinemic Hypoglycemia, Familial, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperinsulinemic Hypoglycemia, Familial, 5 from the curated CTD Gene-Disease Associations dataset.

Familial antiphospholipid syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial antiphospholipid syndrome from the curated CTD Gene-Disease Associations dataset.

Amyloidosis, Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amyloidosis, Familial from the curated CTD Gene-Disease Associations dataset.

Familial paroxysmal dystonia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial paroxysmal dystonia from the curated CTD Gene-Disease Associations dataset.

Atrial fibrillation, familial 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial fibrillation, familial 1 from the curated CTD Gene-Disease Associations dataset.

EPILEPSY, FAMILIAL TEMPORAL LOBE, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 3 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 from the curated CTD Gene-Disease Associations dataset.

Hypercholanemia, Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypercholanemia, Familial from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 from the curated CTD Gene-Disease Associations dataset.

Hyperbilirubinemia, Transient Familial Neonatal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperbilirubinemia, Transient Familial Neonatal from the curated CTD Gene-Disease Associations dataset.

EPILEPSY, FAMILIAL TEMPORAL LOBE, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 2 from the curated CTD Gene-Disease Associations dataset.

Meningioma, familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Meningioma, familial from the curated CTD Gene-Disease Associations dataset.

Aortic Aneurysm, Familial Thoracic 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 6 from the curated CTD Gene-Disease Associations dataset.

Aortic Aneurysm, Familial Thoracic 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 2 from the curated CTD Gene-Disease Associations dataset.

Dysautonomia, Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dysautonomia, Familial from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 1 from the curated CTD Gene-Disease Associations dataset.

Hemophagocytic lymphohistiocytosis, familial, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hemophagocytic lymphohistiocytosis, familial, 3 from the curated CTD Gene-Disease Associations dataset.

Familial Cold Autoinflammatory Syndrome 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial Cold Autoinflammatory Syndrome 2 from the curated CTD Gene-Disease Associations dataset.

Epilepsy, Familial Adult Myoclonic, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, Familial Adult Myoclonic, 3 from the curated CTD Gene-Disease Associations dataset.

Prostate cancer, familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Prostate cancer, familial from the curated CTD Gene-Disease Associations dataset.

Convulsions, Benign Familial Infantile, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Convulsions, Benign Familial Infantile, 4 from the curated CTD Gene-Disease Associations dataset.

Polycythemia, primary familial and congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polycythemia, primary familial and congenital from the curated CTD Gene-Disease Associations dataset.

PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA from the curated CTD Gene-Disease Associations dataset.

Aortic Aneurysm, Familial Thoracic 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 1 from the curated CTD Gene-Disease Associations dataset.

Erythrocytosis, Familial, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Erythrocytosis, Familial, 4 from the curated CTD Gene-Disease Associations dataset.

Hyperinsulinemic hypoglycemia, familial, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperinsulinemic hypoglycemia, familial, 3 from the curated CTD Gene-Disease Associations dataset.

BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.

BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.

Hyperinsulinemic hypoglycemia, familial, 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperinsulinemic hypoglycemia, familial, 7 from the curated CTD Gene-Disease Associations dataset.

CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 from the curated CTD Gene-Disease Associations dataset.

Hyperthyroxinemia, Familial Dysalbuminemic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperthyroxinemia, Familial Dysalbuminemic from the curated CTD Gene-Disease Associations dataset.

Aortic aneurysm, familial thoracic 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aortic aneurysm, familial thoracic 4 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Restrictive, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 2 from the curated CTD Gene-Disease Associations dataset.

Atrial Fibrillation, Familial, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Fibrillation, Familial, 5 from the curated CTD Gene-Disease Associations dataset.

Familial cylindromatosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial cylindromatosis from the curated CTD Gene-Disease Associations dataset.

Familial benign hypercalcemia, type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial benign hypercalcemia, type 3 from the curated CTD Gene-Disease Associations dataset.

Hyperaldosteronism, Familial, Type II Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperaldosteronism, Familial, Type II from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 11 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 11 from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia from the curated CTD Gene-Disease Associations dataset.

Atrial myxoma, familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial myxoma, familial from the curated CTD Gene-Disease Associations dataset.

Familial Glucocorticoid Deficiency 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial Glucocorticoid Deficiency 1 from the curated CTD Gene-Disease Associations dataset.

Tumoral Calcinosis, Normophosphatemic, Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Tumoral Calcinosis, Normophosphatemic, Familial from the curated CTD Gene-Disease Associations dataset.

MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.

Hypocalciuric hypercalcemia, familial, type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypocalciuric hypercalcemia, familial, type 1 from the curated CTD Gene-Disease Associations dataset.

Trichoepithelioma multiple familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Trichoepithelioma multiple familial from the curated CTD Gene-Disease Associations dataset.

Febrile Convulsions, Familial, 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Febrile Convulsions, Familial, 10 from the curated CTD Gene-Disease Associations dataset.

EPILEPSY, FAMILIAL TEMPORAL LOBE, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 1 from the curated CTD Gene-Disease Associations dataset.

EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2 from the curated CTD Gene-Disease Associations dataset.

Hemophagocytic lymphohistiocytosis, familial, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hemophagocytic lymphohistiocytosis, familial, 2 from the curated CTD Gene-Disease Associations dataset.

Periodic fever, familial, autosomal dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Periodic fever, familial, autosomal dominant from the curated CTD Gene-Disease Associations dataset.

VENTRICULAR TACHYCARDIA, FAMILIAL Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease VENTRICULAR TACHYCARDIA, FAMILIAL from the curated CTD Gene-Disease Associations dataset.

Hyperuricemic Nephropathy, Familial Juvenile 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperuricemic Nephropathy, Familial Juvenile 2 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 from the curated CTD Gene-Disease Associations dataset.

Hypobetalipoproteinemia, Familial, Apolipoprotein B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypobetalipoproteinemia, Familial, Apolipoprotein B from the curated CTD Gene-Disease Associations dataset.

Aortic Aneurysm, Familial Abdominal 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aortic Aneurysm, Familial Abdominal 3 from the curated CTD Gene-Disease Associations dataset.

Familial schizencephaly Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial schizencephaly from the curated CTD Gene-Disease Associations dataset.

Atrial Fibrillation, Familial, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Fibrillation, Familial, 2 from the curated CTD Gene-Disease Associations dataset.

HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1 from the curated CTD Gene-Disease Associations dataset.

Neurofibromatosis, Familial Spinal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neurofibromatosis, Familial Spinal from the curated CTD Gene-Disease Associations dataset.

Reticuloendotheliosis, familial, with eosinophilia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Reticuloendotheliosis, familial, with eosinophilia from the curated CTD Gene-Disease Associations dataset.

SEIZURES, BENIGN FAMILIAL NEONATAL, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL NEONATAL, 1 from the curated CTD Gene-Disease Associations dataset.

Advanced Sleep-Phase Syndrome, Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Advanced Sleep-Phase Syndrome, Familial from the curated CTD Gene-Disease Associations dataset.

MIGRAINE, FAMILIAL HEMIPLEGIC, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MIGRAINE, FAMILIAL HEMIPLEGIC, 2 from the curated CTD Gene-Disease Associations dataset.

MIGRAINE, FAMILIAL HEMIPLEGIC, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MIGRAINE, FAMILIAL HEMIPLEGIC, 1 from the curated CTD Gene-Disease Associations dataset.

MITRAL VALVE PROLAPSE, FAMILIAL Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITRAL VALVE PROLAPSE, FAMILIAL from the curated CTD Gene-Disease Associations dataset.

Progressive Familial Heart Block, Type Ib Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Progressive Familial Heart Block, Type Ib from the curated CTD Gene-Disease Associations dataset.

Familial dilated cardiomyopathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial dilated cardiomyopathy from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 from the curated CTD Gene-Disease Associations dataset.

Cholestasis, progressive familial intrahepatic 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 3 from the curated CTD Gene-Disease Associations dataset.

Thymoma, Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thymoma, Familial from the curated CTD Gene-Disease Associations dataset.

Atypical Mycobacteriosis, Familial, X-Linked 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atypical Mycobacteriosis, Familial, X-Linked 1 from the curated CTD Gene-Disease Associations dataset.

Familial Testotoxicosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial Testotoxicosis from the curated CTD Gene-Disease Associations dataset.

Epilepsy, Myoclonic, Benign Adult Familial, Type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, Myoclonic, Benign Adult Familial, Type 1 from the curated CTD Gene-Disease Associations dataset.

Hemiplegic migraine, familial type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hemiplegic migraine, familial type 2 from the curated CTD Gene-Disease Associations dataset.

Hemiplegic migraine, familial type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hemiplegic migraine, familial type 1 from the curated CTD Gene-Disease Associations dataset.

Familial apoceruloplasmin deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial apoceruloplasmin deficiency from the curated CTD Gene-Disease Associations dataset.

HYPERCHOLESTEROLEMIA, FAMILIAL Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HYPERCHOLESTEROLEMIA, FAMILIAL from the curated CTD Gene-Disease Associations dataset.

Amyloid Neuropathies, Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amyloid Neuropathies, Familial from the curated CTD Gene-Disease Associations dataset.

CANDIDIASIS, FAMILIAL, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CANDIDIASIS, FAMILIAL, 2 from the curated CTD Gene-Disease Associations dataset.

Familial Mediterranean Fever Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial Mediterranean Fever from the curated CTD Gene-Disease Associations dataset.

Febrile Convulsions, Familial, 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Febrile Convulsions, Familial, 7 from the curated CTD Gene-Disease Associations dataset.

Febrile Convulsions, Familial, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Febrile Convulsions, Familial, 6 from the curated CTD Gene-Disease Associations dataset.

Febrile Convulsions, Familial, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Febrile Convulsions, Familial, 1 from the curated CTD Gene-Disease Associations dataset.

Cerebral Amyloid Angiopathy, Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral Amyloid Angiopathy, Familial from the curated CTD Gene-Disease Associations dataset.

CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12 from the curated CTD Gene-Disease Associations dataset.

Hypobetalipoproteinemia, Familial, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypobetalipoproteinemia, Familial, 2 from the curated CTD Gene-Disease Associations dataset.

Stuttering, Familial Persistent 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Stuttering, Familial Persistent 2 from the curated CTD Gene-Disease Associations dataset.

Trichoepithelioma, Multiple Familial, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Trichoepithelioma, Multiple Familial, 2 from the curated CTD Gene-Disease Associations dataset.

Epilepsy, Familial Temporal Lobe, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, Familial Temporal Lobe, 4 from the curated CTD Gene-Disease Associations dataset.

MYOCLONIC EPILEPSY, FAMILIAL INFANTILE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MYOCLONIC EPILEPSY, FAMILIAL INFANTILE from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 14 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 14 from the curated CTD Gene-Disease Associations dataset.

familial mediterranean fever Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease familial mediterranean fever from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

familial hyperlipidemia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease familial hyperlipidemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

familial hemiplegic migraine Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease familial hemiplegic migraine from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

familial atrial fibrillation Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease familial atrial fibrillation from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

familial juvenile hyperuricemic nephropathy Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease familial juvenile hyperuricemic nephropathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

familial lipoprotein lipase deficiency Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease familial lipoprotein lipase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

familial periodic paralysis Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease familial periodic paralysis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

familial lipoprotein lipase deficiency Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial lipoprotein lipase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial hypertriglyceridemia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial hypertriglyceridemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

benign familial infantile epilepsy Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease benign familial infantile epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial melanoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial combined hyperlipidemia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial combined hyperlipidemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial renal oncocytoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial renal oncocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

fatal familial insomnia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease fatal familial insomnia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial mediterranean fever Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial mediterranean fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial nephrotic syndrome Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial nephrotic syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial glomangioma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial glomangioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial hyperlipidemia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial hyperlipidemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial hypercholesterolemia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial hypercholesterolemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial periodic paralysis Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial periodic paralysis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial meningioma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial juvenile hyperuricemic nephropathy Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial juvenile hyperuricemic nephropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

benign familial neonatal epilepsy Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease benign familial neonatal epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial partial lipodystrophy Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial partial lipodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial hemiplegic migraine Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial hemiplegic migraine in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial visceral amyloidosis Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial visceral amyloidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial atrial fibrillation Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial atrial fibrillation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial medullary thyroid carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial medullary thyroid carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial renal papillary carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial renal papillary carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial retinoblastoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial retinoblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

arthritis, rheumatoid; familial mediterranean fever; rheumatoid arthritis; rheumatoid spondylitis; spondylitis, ankylosing Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; familial mediterranean fever; rheumatoid arthritis; rheumatoid spondylitis; spondylitis, ankylosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; familial mediterranean fever Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperlipidemia, familial combined Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial mediterranean fever; spondylitis, ankylosing Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial mediterranean fever; spondylitis, ankylosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mild familial hypercholesterolemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mild familial hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial atypical progressive supranuclear palsy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial atypical progressive supranuclear palsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperlipidemia, familial combined; insulin resistance; mixed hyperlipidemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperlipidemia, familial combined; insulin resistance; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial or sporadic prostate cancer. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial or sporadic prostate cancer. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial distal renal tubular acidosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial distal renal tubular acidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abdominal pain; amyloidosis; arthritis; familial mediterranean fever; fever Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abdominal pain; amyloidosis; arthritis; familial mediterranean fever; fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial hypercholesterolemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial defective apolipoprotein b100. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial defective apolipoprotein b100. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma; familial mediterranean fever Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial hypercholesterolaemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial hypercholesterolaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial mediterranean fever; henoch-schoenlein purpura; purpura, schoenlein-henoch Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial mediterranean fever; henoch-schoenlein purpura; purpura, schoenlein-henoch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amyloidosis, familial; cerebral hemorrhage; cerebral hemorrhages Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyloidosis, familial; cerebral hemorrhage; cerebral hemorrhages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial mediterranean fever; glomerulonephritis, iga; iga glomerulonephritides Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial mediterranean fever; glomerulonephritis, iga; iga glomerulonephritides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amyloid neuropathies; amyloid neuropathies, familial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyloid neuropathies; amyloid neuropathies, familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early-onset familial alzheimer's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early-onset familial alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, juvenile rheumatoid; arthritis, psoriatic; familial mediterranean fever; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, juvenile rheumatoid; arthritis, psoriatic; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abdomen, acute; familial mediterranean fever Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abdomen, acute; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; hyperlipidemia, familial combined Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial dysbetalipoproteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial dysbetalipoproteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial defective apolipoprotein b Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial defective apolipoprotein b in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial amyloid polyneuropathy. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial amyloid polyneuropathy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

parkinson's disease (familial) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease parkinson's disease (familial) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mild familial hypercholesterolaemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mild familial hypercholesterolaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial combined hyperlipidemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial combined hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

endogenous hypertriglyceridemia and familial hypercholesterolemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease endogenous hypertriglyceridemia and familial hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial mediterranean fever; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid; leukemia, myeloid, acute; myelodysplastic syndromes; myeloid leukemia; polycythemia vera; preleukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial mediterranean fever; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid; leukemia, myeloid, acute; myelodysplastic syndromes; myeloid leukemia; polycythemia vera; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial type 3 hyperlipoproteinaemia; hyperlipoproteinemia type iii Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial type 3 hyperlipoproteinaemia; hyperlipoproteinemia type iii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial age-related macular degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial age-related macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial premature myocardial infarction. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial premature myocardial infarction. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial mediterranean fever Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial amyloidotic polyneuropathy. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial amyloidotic polyneuropathy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.