| Name |
|---|
MSigDB Cancer Gene Co-expression Modules DatasetFrom Molecular Signatures Database Computational signatures of genes co-expressed with cancer related genes |
MSigDB Signatures of Differentially Expressed Genes for Cancer Gene Perturbations DatasetFrom Molecular Signatures Database Oncogenic signatures of genes differentially expressed following cancer gene perturbations |
Sanger Dependency Map Cancer Cell Line Proteomics DatasetFrom Sanger Cancer Dependency Map Protein intensity values acquired using data-independent acquisition mass spectrometry (DIA-MS). |
CCLE Cell Line Gene CNV Profiles DatasetFrom Cancer Cell Line Encyclopedia Gene-level copy number variation profiles for cancer cell lines |
CCLE Cell Line Gene Expression Profiles DatasetFrom Cancer Cell Line Encyclopedia mRNA microarray expression profiles for cancer cell lines |
CCLE Cell Line Gene Mutation Profiles DatasetFrom Cancer Cell Line Encyclopedia Gene-level mutation profiles for cancer cell lines |
CCLE Cell Line Proteomics DatasetFrom Cancer Cell Line Encyclopedia Protein intensity values acquired using mass spectrometry across human cancerous cell lines |
COSMIC Cell Line Gene CNV Profiles DatasetFrom Catalogue of Somatic Mutations In Cancer Gene-level copy number variation profiles for cancer cell lines |
COSMIC Cell Line Gene Mutation Profiles DatasetFrom Catalogue of Somatic Mutations In Cancer Gene mutations in cancer cell lines from low-throughput or high-throughput studies |
GDSC Cell Line Gene Expression Profiles DatasetFrom Genomics of Drug Sensitivity in Cancer mRNA microarray expression profiles for cancer cell lines |
TCGA Signatures of Differentially Expressed Genes for Tumors DatasetmRNA expression profiles for tumor and normal tissue samples |
DepMap CRISPR Gene Dependency DatasetDependency scores for cell lines following single gene knockdowns |
HPCX Genehereditary prostate cancer, X-linked |
HMN7A GeneMotor neuronopathy, distal hereditary, type VIIA |
HPFH2 Genehereditary persistence of fetal hemoglobin, heterocellular, Indian type |
HHT4 GeneTelangiectasia, hereditary hemorrhagic, type 4 |
HPC5 Geneprostate cancer, hereditary, 5 |
HPC4 GeneProstate cancer, hereditary, 4 |
HPC3 GeneProstate cancer, hereditary, 3 |
HPC7 GeneProstate cancer, hereditary, 7 |
DHS Genedehydrated hereditary stomatocytosis |
GINGF4 Genegingival fibromatosis, hereditary, 4 |
HMSN5 GeneHereditary motor and sensory neuropathy V |
HPC15 GeneProstate cancer, hereditary, 15 |
HPC14 GeneProstate cancer, hereditary, 14 |
HPC10 GeneProstate cancer, hereditary, 10 |
NMSR GeneNeuropathy, hereditary motor and sensory, Russe type |
HPC9 GeneProstate cancer, hereditary, 9 |
LMPH1B GeneLymphedema, hereditary, IB |
HEMC Genehemangioma, capillary, hereditary |
HSN1B GeneHereditary sensory neuropathy, type IB |
HPCX2 GeneProstate cancer, hereditary, X-linked 2 |
PTOS2 GenePtosis, hereditary congenital 2 |
HNB1 Genehereditary neuroblastoma 1 |
ETM3 GeneTremor, hereditary essential, 3 |
HBFQTL2 Genehereditary persistence of fetal hemoglobin, heterocellular |
HMNJ GeneDistal hereditary motor neuropathy, Jerash type |
DKBI GeneDyskeratosis, hereditary benign intraepithelial |
GINGF3 Genegingival fibromatosis, hereditary, 3 |
GINGF2 Genegingival fibromatosis, hereditary, 2 |
HMSNO GeneNeuropathy, hereditary motor and sensory, Okinawa type |
CMAL GeneCapillary malformations, hereditary |
MUHH2 GeneHypotrichosis, hereditary, Marie Unna type, 2 |
ST13P19 Genesuppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) pseudogene 19 |
ST13P18 Genesuppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) pseudogene 18 |
ST13P17 Genesuppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) pseudogene 17 |
ST13P16 Genesuppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) pseudogene 16 |
ST13P15 Genesuppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) pseudogene 15 |
ST13P14 Genesuppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) pseudogene 14 |
ST13P13 Genesuppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) pseudogene 13 |
ST13P12 Genesuppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) pseudogene 12 |
ST13P11 Genesuppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) pseudogene 11 |
ST13P10 Genesuppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) pseudogene 10 |
SDCCAG8 Geneserologically defined colon cancer antigen 8 This gene encodes a centrosome associated protein. This protein may be involved in organizing the centrosome during interphase and mitosis. Mutations in this gene are associated with retinal-renal ciliopathy. [provided by RefSeq, Oct 2010] |
SDCCAG3 Geneserologically defined colon cancer antigen 3 Involved in several processes, including endocytic recycling; positive regulation of cilium assembly; and positive regulation of protein localization to cilium. Located in several cellular components, including endosome; microtubule organizing center; and retromer complex. [provided by Alliance of Genome Resources, Mar 2025] |
ST13P9 Genesuppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) pseudogene 9 |
ST13P8 Genesuppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) pseudogene 8 |
ST13P7 Genesuppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) pseudogene 7 |
ST13P6 Genesuppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) pseudogene 6 |
ST13P5 Genesuppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) pseudogene 5 Predicted to enable protein dimerization activity. Predicted to be located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ST13P4 Genesuppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) pseudogene 4 Predicted to enable protein dimerization activity. Located in extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
ST13P3 Genesuppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) pseudogene 3 |
ST13P2 Genesuppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) pseudogene 2 |
ST13P1 Genesuppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) pseudogene 1 |
CCAT2 Genecolon cancer associated transcript 2 (non-protein coding) This gene produces a long non-coding RNA that is upregulated in colon cancer and other cancers. This transcript promotes cell proliferation and suppresses apoptosis. It negatively regulates the biogenesis of microRNA 145. [provided by RefSeq, Dec 2017] |
MACC1 Genemetastasis associated in colon cancer 1 MACC1 is a key regulator of the hepatocyte growth factor (HGF; MIM 142409)-HGF receptor (HGFR, or MET; MIM 164860) pathway, which is involved in cellular growth, epithelial-mesenchymal transition, angiogenesis, cell motility, invasiveness, and metastasis. Expression of MACC1 in colon cancer (MIM 114500) specimens is an independent prognostic indicator for metastasis formation and metastasis-free survival (Stein et al., 2009 [PubMed 19098908]).[supplied by OMIM, Mar 2009] |
SDCCAG3P2 Geneserologically defined colon cancer antigen 3 pseudogene 2 |
SDCCAG3P1 Geneserologically defined colon cancer antigen 3 pseudogene 1 |
CCAT1 Genecolon cancer associated transcript 1 (non-protein coding) This gene produces a long non-coding RNA that promotes tumor formation and is upregulated in colon cancer and other cancer cell types. This transcript may regulate long range chromosomal interactions, including at the Myc oncoprotein locus. This RNA may also function as a molecular sponge for microRNAs. [provided by RefSeq, Dec 2017] |
ST13P22 Genesuppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) pseudogene 22 |
ST13P20 Genesuppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) pseudogene 20 |
ST13P21 Genesuppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) pseudogene 21 |
CAHM Genecolon adenocarcinoma hypermethylated (non-protein coding) |
ST14 Genesuppression of tumorigenicity 14 (colon carcinoma) The protein encoded by this gene is an epithelial-derived, integral membrane serine protease. This protease forms a complex with the Kunitz-type serine protease inhibitor, HAI-1, and is found to be activated by sphingosine 1-phosphate. This protease has been shown to cleave and activate hepatocyte growth factor/scattering factor, and urokinase plasminogen activator, which suggest the function of this protease as an epithelial membrane activator for other proteases and latent growth factors. The expression of this protease has been associated with breast, colon, prostate, and ovarian tumors, which implicates its role in cancer invasion, and metastasis. [provided by RefSeq, Jul 2008] |
ST13 Genesuppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) The protein encoded by this gene is an adaptor protein that mediates the association of the heat shock proteins HSP70 and HSP90. This protein has been shown to be involved in the assembly process of glucocorticoid receptor, which requires the assistance of multiple molecular chaperones. The expression of this gene is reported to be downregulated in colorectal carcinoma tissue suggesting that it is a candidate tumor suppressor gene. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jun 2013] |
ICT1 Geneimmature colon carcinoma transcript 1 The protein encoded by this gene is a peptidyl-tRNA hydrolase and a vital component of the large mitochondrial ribosome. The encoded protein serves as a ribosome release factor for this ribosome, which translates mitochondrial genes. This protein may be responsible for degrading prematurely-terminated polypeptides and for reusing stalled ribosomes. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2014] |
Hereditary nonpolyposis colon cancer Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary nonpolyposis colon cancer phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
colorectal neoplasms, hereditary nonpolyposis; hereditary nonpolyposis colorectal neoplasms; neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms, hereditary nonpolyposis; hereditary nonpolyposis colorectal neoplasms; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms; hereditary nonpolyposis colorectal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms; hereditary nonpolyposis colorectal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms, hereditary nonpolyposis; hereditary nonpolyposis colorectal neoplasms; neoplasms, second primary; rectal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms, hereditary nonpolyposis; hereditary nonpolyposis colorectal neoplasms; neoplasms, second primary; rectal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms, hereditary nonpolyposis; hereditary nonpolyposis colorectal neoplasms; microsatellite instability Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms, hereditary nonpolyposis; hereditary nonpolyposis colorectal neoplasms; microsatellite instability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms, hereditary nonpolyposis; hereditary nonpolyposis colorectal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms, hereditary nonpolyposis; hereditary nonpolyposis colorectal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary nonpolyposis colon cancer. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary nonpolyposis colon cancer. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; breast cancer; liver cancer; oral cancer; prostate cancer; thyroid cancer; cervical cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; breast cancer; liver cancer; oral cancer; prostate cancer; thyroid cancer; cervical cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; breast cancer; liver cancer; oral cancer; thyroid cancer; cervical cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; breast cancer; liver cancer; oral cancer; thyroid cancer; cervical cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Hereditary nonpolyposis colorectal cancer type 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary nonpolyposis colorectal cancer type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary nonpolyposis colorectal cancer type 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary nonpolyposis colorectal cancer type 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary nonpolyposis colorectal cancer type 7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary nonpolyposis colorectal cancer type 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Colorectal Cancer, Hereditary Nonpolyposis, Type 8 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Colorectal Cancer, Hereditary Nonpolyposis, Type 8 from the curated CTD Gene-Disease Associations dataset. |
colorectal cancer, hereditary nonpolyposis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal cancer, hereditary nonpolyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal cancer, hereditary nonpolyposis, type 7 Gene SetFrom OMIM Gene-Disease Associations genes associated with the colorectal cancer, hereditary nonpolyposis, type 7 phenotype from the curated OMIM Gene-Disease Associations dataset. |
colorectal cancer, hereditary nonpolyposis, type 8 Gene SetFrom OMIM Gene-Disease Associations genes associated with the colorectal cancer, hereditary nonpolyposis, type 8 phenotype from the curated OMIM Gene-Disease Associations dataset. |
colorectal cancer, hereditary nonpolyposis, type 6 Gene SetFrom OMIM Gene-Disease Associations genes associated with the colorectal cancer, hereditary nonpolyposis, type 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
colorectal cancer, hereditary nonpolyposis, type 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the colorectal cancer, hereditary nonpolyposis, type 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
colorectal cancer, hereditary nonpolyposis, type 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the colorectal cancer, hereditary nonpolyposis, type 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
colorectal cancer, hereditary nonpolyposis, type 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the colorectal cancer, hereditary nonpolyposis, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
colorectal cancer, hereditary nonpolyposis, type 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the colorectal cancer, hereditary nonpolyposis, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
Hereditary Nonpolyposis Colorectal Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Nonpolyposis Colorectal Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Colorectal Cancer, Hereditary Nonpolyposis, Type 1 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Colorectal Cancer, Hereditary Nonpolyposis, Type 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary nonpolyposis colorectal cancer type 7 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary nonpolyposis colorectal cancer type 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary nonpolyposis colorectal cancer type 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary nonpolyposis colorectal cancer type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary nonpolyposis colorectal cancer type 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary nonpolyposis colorectal cancer type 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary nonpolyposis colorectal cancer type 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary nonpolyposis colorectal cancer type 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary nonpolyposis colorectal cancer type 6 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary nonpolyposis colorectal cancer type 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary nonpolyposis colorectal cancer type 8 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary nonpolyposis colorectal cancer type 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary cancer-predisposing syndrome:Hereditary cancer-predisposing syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary cancer-predisposing syndrome:Hereditary diffuse gastric cancer Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Hereditary diffuse gastric cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
hereditary non-polyposis colon cancer. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary non-polyposis colon cancer. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Hereditary Non-Polyposis Colon Cancer Type 2 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Non-Polyposis Colon Cancer Type 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
gastrointestinal neoplasms; hht - hereditary hemorrhagic telangiectasia; intestinal polyposis; neoplastic syndromes, hereditary; telangiectasia, hereditary hemorrhagic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gastrointestinal neoplasms; hht - hereditary hemorrhagic telangiectasia; intestinal polyposis; neoplastic syndromes, hereditary; telangiectasia, hereditary hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye diseases, hereditary; hearing impairment; hearing loss; hereditary nephritis; nephritis, hereditary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye diseases, hereditary; hearing impairment; hearing loss; hereditary nephritis; nephritis, hereditary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Colorectal Neoplasms, Hereditary Nonpolyposis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Colorectal Neoplasms, Hereditary Nonpolyposis from the curated CTD Gene-Disease Associations dataset. |
colonic neoplasms; colorectal neoplasms, hereditary nonpolyposis; microsatellite instability Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colonic neoplasms; colorectal neoplasms, hereditary nonpolyposis; microsatellite instability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms, hereditary nonpolyposis; microsatellite instability; rectal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms, hereditary nonpolyposis; microsatellite instability; rectal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anticipation, genetic; colorectal neoplasms, hereditary nonpolyposis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anticipation, genetic; colorectal neoplasms, hereditary nonpolyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; genital neoplasms, female; neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; genital neoplasms, female; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast neoplasms; colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms; colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms, hereditary nonpolyposis; pancreatic neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms, hereditary nonpolyposis; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms, hereditary nonpolyposis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms, hereditary nonpolyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; colonic neoplasms; colorectal neoplasms, hereditary nonpolyposis; microsatellite instability Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; colonic neoplasms; colorectal neoplasms, hereditary nonpolyposis; microsatellite instability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; colorectal neoplasms, hereditary nonpolyposis; microsatellite instability Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; colorectal neoplasms, hereditary nonpolyposis; microsatellite instability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary nonpolyposis colorectal carcinoma Gene SetFrom HPO Gene-Disease Associations genes associated with the hereditary nonpolyposis colorectal carcinoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Colorectal Neoplasms, Hereditary Nonpolyposis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Colorectal Neoplasms, Hereditary Nonpolyposis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hereditary Nonpolyposis Colorectal Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Nonpolyposis Colorectal Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary nonpolyposis colorectal neoplasms Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary nonpolyposis colorectal neoplasms phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hereditary nonpolyposis colorectal carcinoma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary nonpolyposis colorectal carcinoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
colon cancer; rectal cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colon cancer; rectal cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; colorectal cancer; esophageal cancer; head and neck cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; colorectal cancer; esophageal cancer; head and neck cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; breast cancer; bladder cancer; cervical cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; breast cancer; bladder cancer; cervical cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; esophageal cancer; stomach cancer; bladder cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; esophageal cancer; stomach cancer; bladder cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; esophageal cancer; stomach cancer; bladder cancer; warfarin sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; esophageal cancer; stomach cancer; bladder cancer; warfarin sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast cancer; colorectal cancer; esophageal cancer; stomach cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast cancer; colorectal cancer; esophageal cancer; stomach cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypopharyngeal cancer; laryngeal cancer; oral cancer; oropharynx cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypopharyngeal cancer; laryngeal cancer; oral cancer; oropharynx cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia; lung cancer; laryngeal cancer; bladder cancer; oral-pharyngeal cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia; lung cancer; laryngeal cancer; bladder cancer; oral-pharyngeal cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; colorectal cancer; esophageal cancer; stomach cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; colorectal cancer; esophageal cancer; stomach cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal cancer, nonpolyposis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal cancer, nonpolyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colon cancer Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease colon cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
descending colon cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease descending colon cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
colon cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease colon cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
sigmoid colon cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sigmoid colon cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
transverse colon cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease transverse colon cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
ascending colon cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ascending colon cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
diet lifestyle and risk of colon cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diet lifestyle and risk of colon cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal cancer; colon polyps Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal cancer; colon polyps in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colon cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colon cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Cancer of Colon_Intestine - Large Intestine - Colon (MMHCC)_GSE4107 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Cancer of Colon_Intestine - Large Intestine - Colon (MMHCC)_GSE4107 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
PTEN_DELETION_GDS2446_59_human_HCT116 colon cancer cells Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the PTEN_DELETION_GDS2446_59_human_HCT116 colon cancer cells gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
PTEN_DELETION_GDS2446_710_human_HCT116 colon cancer cells Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the PTEN_DELETION_GDS2446_710_human_HCT116 colon cancer cells gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
colon cancer Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease colon cancer in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
colon cancer Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the colon cancer phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
colon cancer Gene SetFrom HPO Gene-Disease Associations genes associated with the colon cancer phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Serologically defined colon cancer antigen 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Serologically defined colon cancer antigen 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Colon cancer-associated Mic1-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Colon cancer-associated Mic1-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
{colon cancer, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {colon cancer, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
colon cancer, somatic Gene SetFrom OMIM Gene-Disease Associations genes associated with the colon cancer, somatic phenotype from the curated OMIM Gene-Disease Associations dataset. |
colon cancer, advanced, somatic Gene SetFrom OMIM Gene-Disease Associations genes associated with the colon cancer, advanced, somatic phenotype from the curated OMIM Gene-Disease Associations dataset. |
Stage Iii Colon Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stage Iii Colon Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stage Iii Colon Cancer Ajcc V7 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stage Iii Colon Cancer Ajcc V7 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stage Iii Colon Cancer Ajcc V8 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stage Iii Colon Cancer Ajcc V8 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stage Iia Colon Cancer Ajcc V7 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stage Iia Colon Cancer Ajcc V7 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stage Iia Colon Cancer Ajcc V8 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stage Iia Colon Cancer Ajcc V8 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stage Ii Colon Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stage Ii Colon Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stage Ii Colon Cancer Ajcc V7 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stage Ii Colon Cancer Ajcc V7 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stage Ii Colon Cancer Ajcc V8 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stage Ii Colon Cancer Ajcc V8 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Colon Cancer Liver Metastasis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Colon Cancer Liver Metastasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stage 0 Colon Cancer Ajcc V6 And V7 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stage 0 Colon Cancer Ajcc V6 And V7 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stage I Colon Cancer Ajcc V6 And V7 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stage I Colon Cancer Ajcc V6 And V7 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stage I Colon Cancer Ajcc V8 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stage I Colon Cancer Ajcc V8 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stage Iv Colon Cancer Ajcc V8 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stage Iv Colon Cancer Ajcc V8 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stage Iiic Colon Cancer Ajcc V7 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stage Iiic Colon Cancer Ajcc V7 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stage Iiic Colon Cancer Ajcc V8 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stage Iiic Colon Cancer Ajcc V8 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Colon Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Colon Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stage, Colon Cancer Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Stage, Colon Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Colon Cancer Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Colon Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Metabolic reprogramming in colon cancer Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Metabolic reprogramming in colon cancer pathway from the WikiPathways Pathways 2024 dataset. |
Colon cancer Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Colon cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Colon cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Colon cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Sigmoid colon cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sigmoid colon cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Ascending colon cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ascending colon cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Transverse colon cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Transverse colon cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Descending colon cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Descending colon cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Colon cancer Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Colon cancer phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Sigmoid colon cancer Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Sigmoid colon cancer phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Colon cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Colon cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Disease free survival in colon cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Disease free survival in colon cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Survival in colon cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Survival in colon cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
leukemia; lung cancer; oropharyngolaryngeal cancers; laryngeal cancer; bladder cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia; lung cancer; oropharyngolaryngeal cancers; laryngeal cancer; bladder cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; breast cancer; colorectal cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; breast cancer; colorectal cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast cancer; colorectal cancer; liver cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast cancer; colorectal cancer; liver cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal cancer; drug hypersensitivity; liver cancer; bladder cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal cancer; drug hypersensitivity; liver cancer; bladder cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis, alcoholic; esophageal cancer; head and neck cancer; liver cancer; pancreatitis, alcoholic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis, alcoholic; esophageal cancer; head and neck cancer; liver cancer; pancreatitis, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
stomach cancer; pancreatic cancer; fallopian cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease stomach cancer; pancreatic cancer; fallopian cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; esophageal cancer; stomach cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; esophageal cancer; stomach cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal cancer; laryngeal cancer; oropharynx cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal cancer; laryngeal cancer; oropharynx cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
urethral cancer; brain cancer; colorectal cancer Gene SetFrom PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease urethral cancer; brain cancer; colorectal cancer from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset. |
Breast cancer, ovarian cancer or prostate cancer (pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Breast cancer, ovarian cancer or prostate cancer (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
corneal dystrophies, hereditary; hereditary corneal dystrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease corneal dystrophies, hereditary; hereditary corneal dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary nephritis; nephritis, hereditary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary nephritis; nephritis, hereditary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
corneal dystrophies, hereditary; hereditary corneal dystrophy; hernia, abdominal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease corneal dystrophies, hereditary; hereditary corneal dystrophy; hernia, abdominal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
optic atrophies, hereditary; optic atrophy, autosomal dominant; optic atrophy, hereditary, leber Gene SetFrom GAD Gene-Disease Associations genes associated with the disease optic atrophies, hereditary; optic atrophy, autosomal dominant; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nonpolyposis Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term nonpolyposis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Prostate cancer, hereditary, 13 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Prostate cancer, hereditary, 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary cancer-predisposing syndrome:Lynch syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary cancer-predisposing syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Von Hippel-Lindau syndrome:Hereditary cancer-predisposing syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Von Hippel-Lindau syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lynch syndrome:Hereditary cancer-predisposing syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary diffuse gastric cancer Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary diffuse gastric cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Prostate cancer, hereditary, 12 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Prostate cancer, hereditary, 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary leiomyomatosis and renal cell cancer Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary leiomyomatosis and renal cell cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary cancer-predisposing syndrome:Peutz-Jeghers syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Peutz-Jeghers syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary cancer-predisposing syndrome:Erythrocytosis, familial, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Erythrocytosis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Prostate cancer, hereditary, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Prostate cancer, hereditary, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Prostate cancer, hereditary, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Prostate cancer, hereditary, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Prostate Cancer, Hereditary, 15 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prostate Cancer, Hereditary, 15 from the curated CTD Gene-Disease Associations dataset. |
Prostate Cancer, Hereditary, 9 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prostate Cancer, Hereditary, 9 from the curated CTD Gene-Disease Associations dataset. |
Prostate Cancer, Hereditary, 8 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prostate Cancer, Hereditary, 8 from the curated CTD Gene-Disease Associations dataset. |
Prostate Cancer, Hereditary, 14 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prostate Cancer, Hereditary, 14 from the curated CTD Gene-Disease Associations dataset. |
Prostate Cancer, Hereditary, 11 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prostate Cancer, Hereditary, 11 from the curated CTD Gene-Disease Associations dataset. |
Prostate Cancer, Hereditary, 13 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prostate Cancer, Hereditary, 13 from the curated CTD Gene-Disease Associations dataset. |
Prostate Cancer, Hereditary, 12 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prostate Cancer, Hereditary, 12 from the curated CTD Gene-Disease Associations dataset. |
PROSTATE CANCER, HEREDITARY, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PROSTATE CANCER, HEREDITARY, 1 from the curated CTD Gene-Disease Associations dataset. |
Prostate Cancer, Hereditary, 10 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prostate Cancer, Hereditary, 10 from the curated CTD Gene-Disease Associations dataset. |
HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER from the curated CTD Gene-Disease Associations dataset. |
Prostate Cancer, Hereditary, X-Linked 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prostate Cancer, Hereditary, X-Linked 2 from the curated CTD Gene-Disease Associations dataset. |
Hereditary Breast and Ovarian Cancer Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Breast and Ovarian Cancer Syndrome from the curated CTD Gene-Disease Associations dataset. |
Prostate Cancer, Hereditary, 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prostate Cancer, Hereditary, 5 from the curated CTD Gene-Disease Associations dataset. |
Prostate Cancer, Hereditary, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prostate Cancer, Hereditary, 4 from the curated CTD Gene-Disease Associations dataset. |
Prostate Cancer, Hereditary, 7 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prostate Cancer, Hereditary, 7 from the curated CTD Gene-Disease Associations dataset. |
Prostate Cancer, Hereditary, 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prostate Cancer, Hereditary, 6 from the curated CTD Gene-Disease Associations dataset. |
Prostate Cancer, Hereditary, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prostate Cancer, Hereditary, 3 from the curated CTD Gene-Disease Associations dataset. |
PROSTATE CANCER, HEREDITARY, X-LINKED 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PROSTATE CANCER, HEREDITARY, X-LINKED 1 from the curated CTD Gene-Disease Associations dataset. |
hereditary breast ovarian cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary breast ovarian cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary and sporadic prostate cancer risk. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary and sporadic prostate cancer risk. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary and sporadic prostate cancer susceptibility. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary and sporadic prostate cancer susceptibility. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
{prostate cancer, hereditary, 7} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {prostate cancer, hereditary, 7} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{prostate cancer, hereditary, 2, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {prostate cancer, hereditary, 2, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{prostate cancer, hereditary, 9} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {prostate cancer, hereditary, 9} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{prostate cancer, hereditary, 12} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {prostate cancer, hereditary, 12} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{prostate cancer, hereditary, 10} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {prostate cancer, hereditary, 10} phenotype from the curated OMIM Gene-Disease Associations dataset. |
prostate cancer, hereditary Gene SetFrom OMIM Gene-Disease Associations genes associated with the prostate cancer, hereditary phenotype from the curated OMIM Gene-Disease Associations dataset. |
{prostate cancer, hereditary, 14} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {prostate cancer, hereditary, 14} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{prostate cancer, hereditary, x-linked 2} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {prostate cancer, hereditary, x-linked 2} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{prostate cancer, hereditary, 15} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {prostate cancer, hereditary, 15} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{prostate cancer, hereditary, 13} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {prostate cancer, hereditary, 13} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{prostate cancer, hereditary, 5} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {prostate cancer, hereditary, 5} phenotype from the curated OMIM Gene-Disease Associations dataset. |
Hereditary Leiomyomatosis And Renal Cell Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Leiomyomatosis And Renal Cell Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Breast And Ovarian Cancer Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Breast And Ovarian Cancer Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Diffuse Gastric Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Diffuse Gastric Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Non-Polyposis Colorectal Cancer Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Non-Polyposis Colorectal Cancer Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Site-Specific Ovarian Cancer Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Site-Specific Ovarian Cancer Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Breast/Ovarian Cancer - Brca1 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Breast/Ovarian Cancer - Brca1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Renal Cancer Associated 1 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Renal Cancer Associated 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary diffuse gastric cancer Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary diffuse gastric cancer from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary breast ovarian cancer syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary breast ovarian cancer syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary diffuse gastric cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary diffuse gastric cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary cancer-predisposing syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hereditary breast ovarian cancer syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary breast ovarian cancer syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hereditary thrombocytopenia and hematologic cancer predisposition syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary thrombocytopenia and hematologic cancer predisposition syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hereditary leiomyomatosis and renal cell cancer Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary leiomyomatosis and renal cell cancer phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hereditary cancer Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary cancer phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hereditary site-specific ovarian cancer syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary site-specific ovarian cancer syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hereditary breast cancer Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary breast cancer phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hereditary renal cancer Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary renal cancer phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
colon Gene SetFrom BioGPS Human Cell Type and Tissue Gene Expression Profiles genes with high or low expression in colon relative to other cell types and tissues from the BioGPS Human Cell Type and Tissue Gene Expression Profiles dataset. |
Carcinoma of colon Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Carcinoma of colon phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
colon adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease colon adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
colon carcinoma in situ Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease colon carcinoma in situ in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
colon carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease colon carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
colon neuroendocrine neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease colon neuroendocrine neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lipoma of colon Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lipoma of colon in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
colon mucinous adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease colon mucinous adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
colon lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease colon lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
colon adenomas/carcinomas Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colon adenomas/carcinomas in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colon polyps Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colon polyps in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colon Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term colon in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Crohn's disease_Intestine - Large Intestine - Colon (MMHCC)_GSE6731 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Crohn's disease_Intestine - Large Intestine - Colon (MMHCC)_GSE6731 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
colon epithelial cell migration Gene SetFrom GO Biological Process Annotations 2015 genes participating in the colon epithelial cell migration biological process from the curated GO Biological Process Annotations 2015 dataset. |
colon Gene SetFrom GTEx Tissue Gene Expression Profiles genes with high or low expression in colon relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset. |
neoplasm of the colon Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the neoplasm of the colon phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
colon Gene SetFrom HPA Tissue Gene Expression Profiles genes with high or low expression in colon relative to other tissues from the HPA Tissue Gene Expression Profiles dataset. |
colon Gene SetFrom HPA Tissue Protein Expression Profiles proteins with high or low expression in colon relative to other tissues from the HPA Tissue Protein Expression Profiles dataset. |
malrotation of colon Gene SetFrom HPO Gene-Disease Associations genes associated with the malrotation of colon phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neoplasm of the colon Gene SetFrom HPO Gene-Disease Associations genes associated with the neoplasm of the colon phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the colon Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the colon phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Overexpressed in colon carcinoma 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Overexpressed in colon carcinoma 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
increased colon adenocarcinoma incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased colon adenocarcinoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
colon polyps Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the colon polyps phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased colon tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased colon tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased colon hamartoma incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased colon hamartoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal colon morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal colon morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
colon Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term colon in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
colon Gene SetFrom ProteomicsDB Cell Type and Tissue Protein Expression Profiles proteins with high or low expression in colon relative to other cell types and tissues from the ProteomicsDB Cell Type and Tissue Protein Expression Profiles dataset. |
colon Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue colon from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
colon muscle Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue colon muscle from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
colon Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue colon in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset. |
colon ascendens Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue colon ascendens in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
right colon Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue right colon in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
right colon mucosa Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue right colon mucosa in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
colon-26 cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue colon-26 cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
colon Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue colon in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
colon muscle Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue colon muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
colon transversum Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue colon transversum in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
colon sigmoideum Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue colon sigmoideum in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
left colon Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue left colon in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
colon descendens Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue colon descendens in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Colon Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Colon Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Tumor Of Colon Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Tumor Of Colon in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Colon Adenocarcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Colon Adenocarcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Malignant Neoplasm Of Colon And/Or Rectum Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Colon And/Or Rectum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Functional Diarrhoea (Due To Spastic Colon) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Functional Diarrhoea (Due To Spastic Colon) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Colon Adenoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Colon Adenoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Angiodysplasia Of Colon Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Angiodysplasia Of Colon in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adenomatous Polyp Of Colon Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adenomatous Polyp Of Colon in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Adenocarcinoma Of Colon Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Adenocarcinoma Of Colon in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aganglionosis, Rectosigmoid Colon Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aganglionosis, Rectosigmoid Colon in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Diverticular Disease Of Colon Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Diverticular Disease Of Colon in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Metastatic Colon Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Metastatic Colon Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Benign Neoplasm Of Colon Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Benign Neoplasm Of Colon in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stage I Colon Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stage I Colon Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Diagnosis For Colon Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Diagnosis For Colon in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mucinous Adenocarcinoma Of Colon Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mucinous Adenocarcinoma Of Colon in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Obstruction Of Colon Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Obstruction Of Colon in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Perforation Of Colon Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Perforation Of Colon in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dysplasia Of Colon Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dysplasia Of Colon in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Colon Neuroendocrine Tumor G1 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Colon Neuroendocrine Tumor G1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Colon (Non-Specific) Lesion Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Colon (Non-Specific) Lesion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Tubular Adenoma Of Colon Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Tubular Adenoma Of Colon in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malrotation Of Colon Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malrotation Of Colon in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Colon Mucosa-Associated Lymphoid Tissue Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Colon Mucosa-Associated Lymphoid Tissue Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stage Iv Colon Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stage Iv Colon Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Atresia Of Colon Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Atresia Of Colon in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Colon Serrated Polyposis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Colon Serrated Polyposis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Squamous Cell Carcinoma Of Colon Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Squamous Cell Carcinoma Of Colon in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polyp Of Sigmoid Colon Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polyp Of Sigmoid Colon in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Colon Carcinoma Metastatic In The Liver Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Colon Carcinoma Metastatic In The Liver in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ulceration Of Colon Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ulceration Of Colon in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Colon Diverticulum Anatomic Structure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Colon Diverticulum Anatomic Structure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Colon (Non-Specific) Polyp Hyperplastic Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Colon (Non-Specific) Polyp Hyperplastic in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Colon Growth Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Colon Growth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
colon epithelial cell migration Gene SetFrom GO Biological Process Annotations 2023 genes participating in the colon epithelial cell migration biological process from the curated GO Biological Process Annotations 2023 dataset. |
ATF3-27146783-CHIP-SEQ-COLON-HUMAN Gene SetFrom ChEA Transcription Factor Targets 2022 target genes of the ATF3-27146783-CHIP-SEQ-COLON-HUMAN transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset. |
HNF1A-26855178-CACO2-HUMAN-COLON-ADENOCARCINOMA Gene SetFrom ChEA Transcription Factor Targets 2022 target genes of the HNF1A-26855178-CACO2-HUMAN-COLON-ADENOCARCINOMA transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset. |
abnormal colon morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal colon morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
colon polyps Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the colon polyps phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal colon goblet cell morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal colon goblet cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased colon adenoma incidence Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased colon adenoma incidence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent colon Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent colon phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased colon length Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased colon length phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased colon length Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased colon length phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased colon hamartoma incidence Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased colon hamartoma incidence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased colon adenocarcinoma incidence Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased colon adenocarcinoma incidence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
colon atresia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the colon atresia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased colon tumor incidence Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased colon tumor incidence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased colon goblet cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased colon goblet cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased colon goblet cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased colon goblet cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal colon morphology Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal colon morphology phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Colon - Transverse Gene SetFrom GTEx Tissue Gene Expression Profiles 2023 genes with high or low expression in Colon - Transverse relative to other tissues from the GTEx Tissue Gene Expression Profiles 2023 dataset. |
Colon - Sigmoid Gene SetFrom GTEx Tissue Gene Expression Profiles 2023 genes with high or low expression in Colon - Sigmoid relative to other tissues from the GTEx Tissue Gene Expression Profiles 2023 dataset. |
GTEx Colon 20-29 vs 60-69 Gene SetFrom GTEx Tissue-Specific Aging Signatures genes with high or low expression in GTEx Colon 20-29 vs 60-69 relative to other tissue samples from the GTEx Tissue-Specific Aging Signatures dataset. |
GTEx Colon 20-29 vs 50-59 Gene SetFrom GTEx Tissue-Specific Aging Signatures genes with high or low expression in GTEx Colon 20-29 vs 50-59 relative to other tissue samples from the GTEx Tissue-Specific Aging Signatures dataset. |
GTEx Colon 20-29 vs 70-79 Gene SetFrom GTEx Tissue-Specific Aging Signatures genes with high or low expression in GTEx Colon 20-29 vs 70-79 relative to other tissue samples from the GTEx Tissue-Specific Aging Signatures dataset. |
GTEx Colon 20-29 vs 40-49 Gene SetFrom GTEx Tissue-Specific Aging Signatures genes with high or low expression in GTEx Colon 20-29 vs 40-49 relative to other tissue samples from the GTEx Tissue-Specific Aging Signatures dataset. |
colon epithelial cell migration Gene SetFrom GO Biological Process Annotations 2025 genes participating in the colon epithelial cell migration biological process from the curated GO Biological Process Annotations 2025 dataset. |
Colon carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Colon carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Colon adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Colon adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Colon lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Colon lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Colon mucinous adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Colon mucinous adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Colon adenoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Colon adenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Diverticulitis of colon Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diverticulitis of colon in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Colon carcinoma in situ Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Colon carcinoma in situ in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Medullary colon carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Medullary colon carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Adenosquamous colon carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Adenosquamous colon carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Colon neuroendocrine neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Colon neuroendocrine neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Colon squamous cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Colon squamous cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lipoma of colon Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lipoma of colon in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Colon small cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Colon small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Colon Kaposi sarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Colon Kaposi sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Colon sarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Colon sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Colon leiomyosarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Colon leiomyosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Colon leiomyoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Colon leiomyoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Colon Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Colon from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Colon muscle Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Colon muscle from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Colon Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Colon in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset. |
Colon Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Colon in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Right colon Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Right colon in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Colon sigmoideum Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Colon sigmoideum in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Colon transversum Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Colon transversum in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Left colon Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Left colon in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Colon ascendens Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Colon ascendens in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Colon descendens Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Colon descendens in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Colon muscle Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Colon muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Colon-26 cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Colon-26 cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Right colon mucosa Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Right colon mucosa in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Colon 26-L5 cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Colon 26-L5 cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Carcinoma of colon Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Carcinoma of colon phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Colon adenocarcinoma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Colon adenocarcinoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Malignant tumor of ascending colon Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Malignant tumor of ascending colon phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Polyp of colon Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Polyp of colon phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Adenomatous polyp of colon Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Adenomatous polyp of colon phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
PROSTATE CANCER/BRAIN CANCER SUSCEPTIBILITY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PROSTATE CANCER/BRAIN CANCER SUSCEPTIBILITY from the curated CTD Gene-Disease Associations dataset. |
cancer; colorectal cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cancer; colorectal cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal cancer; stomach cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal cancer; stomach cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ovarian cancer ; breast cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ovarian cancer ; breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast cancer; endometrial cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast cancer; endometrial cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal cancer; oropharyngolaryngeal cancers; stomach cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal cancer; oropharyngolaryngeal cancers; stomach cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal cancer; stomach cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal cancer; stomach cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast cancer; cytogenetic studies; prostate cancer; longevity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast cancer; cytogenetic studies; prostate cancer; longevity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; skin cancer, non-melanoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; skin cancer, non-melanoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
kidney cancer; bladder cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease kidney cancer; bladder cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast cancer; ovarian cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast cancer; ovarian cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal cancer; esophageal cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal cancer; esophageal cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; breast cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cancer; breast cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cancer; breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ovarian cancer; thyroid cancer; pheochromocytoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ovarian cancer; thyroid cancer; pheochromocytoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal cancer; gastric cardia cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal cancer; gastric cardia cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
liver cancer; nasopharyngeal cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease liver cancer; nasopharyngeal cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
prostate cancer ; breast cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease prostate cancer ; breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal cancer; stomach cancer; barret's esophagus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal cancer; stomach cancer; barret's esophagus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary duct stones; biliary tract cancer; gallbladder cancer; gallstones Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary duct stones; biliary tract cancer; gallbladder cancer; gallstones in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; bladder cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; bladder cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal cancer; gastric cardiac cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal cancer; gastric cardiac cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal cancer; endometrial cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal cancer; endometrial cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
stomach cancer; ovarian cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease stomach cancer; ovarian cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bladder cancer; prostate cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bladder cancer; prostate cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast cancer; colorectal cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast cancer; colorectal cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
prostate cancer; ovarian cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease prostate cancer; ovarian cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal cancer ; lung cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal cancer ; lung cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal cancer and lung cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal cancer and lung cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; liver cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; liver cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal cancer; cardiac cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal cancer; cardiac cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast cancer ovarian cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast cancer ovarian cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast cancer; prostate cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast cancer; prostate cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cancer; lung cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cancer; lung cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; esophageal cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; esophageal cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Esophageal cancer and gastric cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Esophageal cancer and gastric cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Multiple cancers (lung cancer, gastric cancer, and squamous cell carcinoma) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Multiple cancers (lung cancer, gastric cancer, and squamous cell carcinoma) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
{prostate cancer/brain cancer susceptibility, somatic} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {prostate cancer/brain cancer susceptibility, somatic} phenotype from the curated OMIM Gene-Disease Associations dataset. |
breast cancer; colorectal cancer Gene SetFrom PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease breast cancer; colorectal cancer from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset. |
Inherited breast cancer and ovarian cancer Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Inherited breast cancer and ovarian cancer phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Prostate cancer/brain cancer susceptibility Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Prostate cancer/brain cancer susceptibility phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Multiple cancers (lung cancer, gastric cancer, and squamous cell carcinoma) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple cancers (lung cancer, gastric cancer, and squamous cell carcinoma) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Esophageal cancer and gastric cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Esophageal cancer and gastric cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Breast cancer and/or colorectal cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Breast cancer and/or colorectal cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Breast cancer in childhood cancer survivors treated with less than 10 gray radiotherapy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Breast cancer in childhood cancer survivors treated with less than 10 gray radiotherapy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Breast cancer in childhood cancer survivors treated with more than 10 gray radiotherapy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Breast cancer in childhood cancer survivors treated with more than 10 gray radiotherapy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Breast cancer in childhood cancer survivors Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Breast cancer in childhood cancer survivors phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pulmonary hypertension, primary, 1, with hereditary hemorrhagic telangiectasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pulmonary hypertension, primary, 1, with hereditary hemorrhagic telangiectasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary acrodermatitis enteropathica Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary acrodermatitis enteropathica phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary liability to pressure palsies Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary liability to pressure palsies phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Telangiectasia, hereditary hemorrhagic, type 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Telangiectasia, hereditary hemorrhagic, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary neutrophilia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary neutrophilia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Facial paresis, hereditary congenital, 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Facial paresis, hereditary congenital, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary sideroblastic anemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary sideroblastic anemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary hemochromatosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary hemochromatosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary C1 esterase inhibitor deficiency - dysfunctional factor phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Neuropathy hereditary sensory and autonomic type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neuropathy hereditary sensory and autonomic type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary hemorrhagic telangiectasia type 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary hemorrhagic telangiectasia type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy 2D Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary Paraganglioma-Pheochromocytoma Syndromes Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary Paraganglioma-Pheochromocytoma Syndromes phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary fructosuria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary fructosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary neuralgic amyotrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary neuralgic amyotrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pulmonary arterial hypertension related to hereditary hemorrhagic telangiectasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pulmonary arterial hypertension related to hereditary hemorrhagic telangiectasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Neuropathy, hereditary motor and sensory, Okinawa type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neuropathy, hereditary motor and sensory, Okinawa type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dominant hereditary optic atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dominant hereditary optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary factor II deficiency disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor II deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY, TYPE IE Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY, TYPE IE phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY, TYPE ID Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY, TYPE ID phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY, TYPE IF Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY, TYPE IF phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alpha-fetoprotein, hereditary persistence of Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alpha-fetoprotein, hereditary persistence of phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary lymphedema type I Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary lymphedema type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary diffuse leukoencephalopathy with spheroids Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary diffuse leukoencephalopathy with spheroids phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy with lactic acidosis, hereditary Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy with lactic acidosis, hereditary phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Tremor, hereditary essential, 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Tremor, hereditary essential, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary Paragangliomas and Pheochromocytomas Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary Paragangliomas and Pheochromocytomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy type 2A Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy type 2C Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy type 2B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary factor IX deficiency disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor IX deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lymphedema, hereditary, ic Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lymphedema, hereditary, ic phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lymphedema, hereditary, id Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lymphedema, hereditary, id phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary myopathy with early respiratory failure Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary myopathy with early respiratory failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy type 5B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 5B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary motor and sensory neuropathy with optic atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary motor and sensory neuropathy with optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary gingival fibromatosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary gingival fibromatosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary factor XI deficiency disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor XI deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary angioedema type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary angioedema type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Marie Unna hereditary hypotrichosis 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Marie Unna hereditary hypotrichosis 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary pyropoikilocytosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary pyropoikilocytosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy type 7B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 7B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY, TYPE IC Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY, TYPE IC phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperekplexia hereditary Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperekplexia hereditary phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary insensitivity to pain with anhidrosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary insensitivity to pain with anhidrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Infantile-onset ascending hereditary spastic paralysis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Infantile-onset ascending hereditary spastic paralysis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked hereditary motor and sensory neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked hereditary motor and sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary hemorrhagic telangiectasia type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary hemorrhagic telangiectasia type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy type 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary pancreatitis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary pancreatitis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary factor VIII deficiency disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor VIII deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thrombophilia, hereditary, due to protein C deficiency, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thrombophilia, hereditary, due to protein C deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary sensory and autonomic neuropathy type IIA Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary sensory and autonomic neuropathy type IIA phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary cerebral amyloid angiopathy, Icelandic type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary cerebral amyloid angiopathy, Icelandic type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary renal agenesis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary renal agenesis from the curated CTD Gene-Disease Associations dataset. |
Dyskeratosis, Hereditary Benign Intraepithelial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Dyskeratosis, Hereditary Benign Intraepithelial from the curated CTD Gene-Disease Associations dataset. |
Tremor hereditary essential, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Tremor hereditary essential, 1 from the curated CTD Gene-Disease Associations dataset. |
Hereditary Sensory and Motor Neuropathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Sensory and Motor Neuropathy from the curated CTD Gene-Disease Associations dataset. |
Hyperexplexia hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyperexplexia hereditary from the curated CTD Gene-Disease Associations dataset. |
Angioedemas, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Angioedemas, Hereditary from the curated CTD Gene-Disease Associations dataset. |
Optic Atrophy, Hereditary, Leber Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy, Hereditary, Leber from the curated CTD Gene-Disease Associations dataset. |
Eye Diseases, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Eye Diseases, Hereditary from the curated CTD Gene-Disease Associations dataset. |
Facial paresis, hereditary, congenital Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Facial paresis, hereditary, congenital from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, Hereditary Sensory And Autonomic, Type IIB Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type IIB from the curated CTD Gene-Disease Associations dataset. |
Cerebral hemorrhage with amyloidosis, hereditary, Dutch type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral hemorrhage with amyloidosis, hereditary, Dutch type from the curated CTD Gene-Disease Associations dataset. |
Thrombophilia, hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Thrombophilia, hereditary from the curated CTD Gene-Disease Associations dataset. |
Elliptocytosis, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Elliptocytosis, Hereditary from the curated CTD Gene-Disease Associations dataset. |
Hyperferritinemia, hereditary, with congenital cataracts Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyperferritinemia, hereditary, with congenital cataracts from the curated CTD Gene-Disease Associations dataset. |
Hypophosphatemic Rickets with Hypercalciuria, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypophosphatemic Rickets with Hypercalciuria, Hereditary from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, hereditary motor and sensory, Russe type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, hereditary motor and sensory, Russe type from the curated CTD Gene-Disease Associations dataset. |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities from the curated CTD Gene-Disease Associations dataset. |
Tremor hereditary essential, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Tremor hereditary essential, 2 from the curated CTD Gene-Disease Associations dataset. |
Polyposis Syndrome, Hereditary Mixed, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Polyposis Syndrome, Hereditary Mixed, 2 from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, Distal Hereditary Motor, Type IIA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Distal Hereditary Motor, Type IIA from the curated CTD Gene-Disease Associations dataset. |
Osteolysis hereditary multicentric Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Osteolysis hereditary multicentric from the curated CTD Gene-Disease Associations dataset. |
Hereditary spastic paralysis, infantile onset ascending Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary spastic paralysis, infantile onset ascending from the curated CTD Gene-Disease Associations dataset. |
Folate Malabsorption, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Folate Malabsorption, Hereditary from the curated CTD Gene-Disease Associations dataset. |
Bullous Dystrophy, Hereditary Macular Type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bullous Dystrophy, Hereditary Macular Type from the curated CTD Gene-Disease Associations dataset. |
Amyloidosis, Hereditary, Transthyretin-Related Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Amyloidosis, Hereditary, Transthyretin-Related from the curated CTD Gene-Disease Associations dataset. |
Neutrophilia, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neutrophilia, Hereditary from the curated CTD Gene-Disease Associations dataset. |
Polyostotic osteolytic dysplasia, hereditary expansile Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Polyostotic osteolytic dysplasia, hereditary expansile from the curated CTD Gene-Disease Associations dataset. |
Ptosis, Hereditary Congenital 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ptosis, Hereditary Congenital 1 from the curated CTD Gene-Disease Associations dataset. |
Optic Atrophies, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophies, Hereditary from the curated CTD Gene-Disease Associations dataset. |
Telangiectasia, Hereditary Hemorrhagic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Telangiectasia, Hereditary Hemorrhagic from the curated CTD Gene-Disease Associations dataset. |
Neuronopathy, Distal Hereditary Motor, Type V Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuronopathy, Distal Hereditary Motor, Type V from the curated CTD Gene-Disease Associations dataset. |
Exostoses, Multiple Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Exostoses, Multiple Hereditary from the curated CTD Gene-Disease Associations dataset. |
Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps from the curated CTD Gene-Disease Associations dataset. |
Neuronopathy, Distal Hereditary Motor, Type IIB Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuronopathy, Distal Hereditary Motor, Type IIB from the curated CTD Gene-Disease Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA from the curated CTD Gene-Disease Associations dataset. |
Hereditary Motor And Sensory Neuropathy, Type IIC Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Motor And Sensory Neuropathy, Type IIC from the curated CTD Gene-Disease Associations dataset. |
Hereditary Motor And Sensory Neuropathy VI Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Motor And Sensory Neuropathy VI from the curated CTD Gene-Disease Associations dataset. |
Hereditary Angioedema Type III Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Angioedema Type III from the curated CTD Gene-Disease Associations dataset. |
LYMPHEDEMA, HEREDITARY, IC Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease LYMPHEDEMA, HEREDITARY, IC from the curated CTD Gene-Disease Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, hereditary motor and sensory, Okinawa type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, hereditary motor and sensory, Okinawa type from the curated CTD Gene-Disease Associations dataset. |
Hereditary Autoinflammatory Diseases Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Autoinflammatory Diseases from the curated CTD Gene-Disease Associations dataset. |
Ptosis, Hereditary Congenital 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ptosis, Hereditary Congenital 2 from the curated CTD Gene-Disease Associations dataset. |
Lymphedema, Hereditary, II Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lymphedema, Hereditary, II from the curated CTD Gene-Disease Associations dataset. |
Lymphedema, Hereditary, IB Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lymphedema, Hereditary, IB from the curated CTD Gene-Disease Associations dataset. |
Hereditary Myopathy with Early Respiratory Failure Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Myopathy with Early Respiratory Failure from the curated CTD Gene-Disease Associations dataset. |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC from the curated CTD Gene-Disease Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC from the curated CTD Gene-Disease Associations dataset. |
Coproporphyria, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Coproporphyria, Hereditary from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset. |
Spherocytosis, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spherocytosis, Hereditary from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, Distal Hereditary Motor, Type VIIA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Distal Hereditary Motor, Type VIIA from the curated CTD Gene-Disease Associations dataset. |
Juvenile Polyposis with Hereditary Hemorrhagic Telangiectasia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Juvenile Polyposis with Hereditary Hemorrhagic Telangiectasia from the curated CTD Gene-Disease Associations dataset. |
Keratitis, hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Keratitis, hereditary from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux from the curated CTD Gene-Disease Associations dataset. |
Myopathy with Lactic Acidosis, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy with Lactic Acidosis, Hereditary from the curated CTD Gene-Disease Associations dataset. |
Leukokeratosis, Hereditary Mucosal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Leukokeratosis, Hereditary Mucosal from the curated CTD Gene-Disease Associations dataset. |
Spastic Paraplegia, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia, Hereditary from the curated CTD Gene-Disease Associations dataset. |
Neuronopathy, Distal Hereditary Motor, Type Viib Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuronopathy, Distal Hereditary Motor, Type Viib from the curated CTD Gene-Disease Associations dataset. |
Hereditary pancreatitis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary pancreatitis from the curated CTD Gene-Disease Associations dataset. |
Albright's hereditary osteodystrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Albright's hereditary osteodystrophy from the curated CTD Gene-Disease Associations dataset. |
Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, and Perinatal Edema Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, and Perinatal Edema from the curated CTD Gene-Disease Associations dataset. |
Adrenocortical Carcinoma, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Adrenocortical Carcinoma, Hereditary from the curated CTD Gene-Disease Associations dataset. |
Hereditary macular coloboma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary macular coloboma from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, hereditary motor and sensory, LOM type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, hereditary motor and sensory, LOM type from the curated CTD Gene-Disease Associations dataset. |
Hereditary Angioedema Types I and II Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Angioedema Types I and II from the curated CTD Gene-Disease Associations dataset. |
Desmoid disease, hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Desmoid disease, hereditary from the curated CTD Gene-Disease Associations dataset. |
Telangiectasia, Hereditary Hemorrhagic, Type 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Telangiectasia, Hereditary Hemorrhagic, Type 4 from the curated CTD Gene-Disease Associations dataset. |
Nephritis, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Nephritis, Hereditary from the curated CTD Gene-Disease Associations dataset. |
Hereditary Sensory and Autonomic Neuropathies Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Sensory and Autonomic Neuropathies from the curated CTD Gene-Disease Associations dataset. |
Pyropoikilocytosis, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pyropoikilocytosis, Hereditary from the curated CTD Gene-Disease Associations dataset. |
Corneal Dystrophies, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophies, Hereditary from the curated CTD Gene-Disease Associations dataset. |
Telangiectasia, Hereditary Benign Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Telangiectasia, Hereditary Benign from the curated CTD Gene-Disease Associations dataset. |
hereditary spherocytosis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hereditary spherocytosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
hereditary hemorrhagic telangiectasia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hereditary hemorrhagic telangiectasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
hereditary spastic paraplegia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hereditary spastic paraplegia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
hereditary elliptocytosis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hereditary elliptocytosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
hereditary angioedema Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hereditary angioedema from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
hereditary sensory neuropathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hereditary sensory neuropathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
hereditary fructose intolerance syndrome Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hereditary fructose intolerance syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
hereditary lymphedema Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hereditary lymphedema from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
hereditary mucosal leukokeratosis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hereditary mucosal leukokeratosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
hereditary multiple exostoses Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hereditary multiple exostoses from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
hereditary sensory neuropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary sensory neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary renal cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary renal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary lymphedema Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary lymphedema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary multiple exostoses Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary multiple exostoses in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary hemorrhagic telangiectasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary hemorrhagic telangiectasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary spastic paraplegia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary spastic paraplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
albright's hereditary osteodystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease albright's hereditary osteodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary retinal dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary retinal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary elliptocytosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary elliptocytosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary angioedema Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary angioedema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary night blindness Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary night blindness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
central nervous system hereditary degenerative disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system hereditary degenerative disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary wilms' tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary wilms' tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary conventional renal cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary conventional renal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary spherocytosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary spherocytosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
leber hereditary optic neuropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease leber hereditary optic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
distal hereditary motor neuropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease distal hereditary motor neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary mucosal leukokeratosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary mucosal leukokeratosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary choroidal atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary choroidal atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary fructose intolerance syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary fructose intolerance syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary coproporphyria Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary coproporphyria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary medullary thyroid carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary medullary thyroid carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary fructose intolerance. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary fructose intolerance. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
neuropathy, hereditary motor and sensory Gene SetFrom GAD Gene-Disease Associations genes associated with the disease neuropathy, hereditary motor and sensory in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary nonspherocytic hemolytic anemia (hnsha). Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary nonspherocytic hemolytic anemia (hnsha). in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
macular degeneration; nephritis, hereditary; retinal degeneration; retinal drusen Gene SetFrom GAD Gene-Disease Associations genes associated with the disease macular degeneration; nephritis, hereditary; retinal degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
neoplastic syndromes, hereditary; pancreatic neoplasm; pancreatic neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease neoplastic syndromes, hereditary; pancreatic neoplasm; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye diseases, hereditary; macular degeneration; retinal degeneration Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye diseases, hereditary; macular degeneration; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
corneal dystrophies, hereditary; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease corneal dystrophies, hereditary; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leber's hereditary optic neuropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leber's hereditary optic neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diseases; hereditary central nervous system demyelinating diseases; leukoencephalopathies Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diseases; hereditary central nervous system demyelinating diseases; leukoencephalopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hemorrhagic telangiectasia, hereditary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hemorrhagic telangiectasia, hereditary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperbilirubinemia, hereditary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperbilirubinemia, hereditary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary stomatocytosis. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary stomatocytosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye diseases, hereditary; genetic diseases, x-linked; nystagmus, congenital; nystagmus, pathologic; strabismus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye diseases, hereditary; genetic diseases, x-linked; nystagmus, congenital; nystagmus, pathologic; strabismus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary hemochromatosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary hemochromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary hemochromatosis in african americans. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary hemochromatosis in african americans. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arteriovenous malformations; liver diseases; telangiectasia, hereditary hemorrhagic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arteriovenous malformations; liver diseases; telangiectasia, hereditary hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary spastic paraparesis due to a frame shift mutat Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary spastic paraparesis due to a frame shift mutat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary spherocytosis (protein 4.2notame). Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary spherocytosis (protein 4.2notame). in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary hemolytic anemia. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary hemolytic anemia. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary hemochromatosis. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary hemochromatosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alpha thalassemia; alpha-thalassemia; elliptocytosis, hereditary; malaria, falciparum Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alpha thalassemia; alpha-thalassemia; elliptocytosis, hereditary; malaria, falciparum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast neoplasms; carcinoma; melanoma; neoplastic syndromes, hereditary; ovarian neoplasms; pancreatic neoplasms; prostatic neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms; carcinoma; melanoma; neoplastic syndromes, hereditary; ovarian neoplasms; pancreatic neoplasms; prostatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blindness; optic atrophy, hereditary, leber Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blindness; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary autoinflammatory diseases; lymphadenitis; pharyngitis; stomatitis, aphthous; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary autoinflammatory diseases; lymphadenitis; pharyngitis; stomatitis, aphthous; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary haemolytic anaemia. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary haemolytic anaemia. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic kidney diseases; kidney diseases, cystic; leber congenital amaurosis; optic atrophies, hereditary; vision disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic kidney diseases; kidney diseases, cystic; leber congenital amaurosis; optic atrophies, hereditary; vision disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
elliptocytosis, hereditary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease elliptocytosis, hereditary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
stickler syndrome (hereditary arthro-ophthalmopathy) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease stickler syndrome (hereditary arthro-ophthalmopathy) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
albright hereditary osteodystrophy; pseudohypoparathyroidism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease albright hereditary osteodystrophy; pseudohypoparathyroidism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary dementia. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary dementia. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
telangiectasia, hereditary hemorrhagic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease telangiectasia, hereditary hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
charcot-marie-tooth disease; hereditary sensory and motor neuropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
heart diseases; hyperplasia; liver diseases; telangiectasia, hereditary hemorrhagic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease heart diseases; hyperplasia; liver diseases; telangiectasia, hereditary hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast neoplasms; neoplastic syndromes, hereditary; ovarian neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms; neoplastic syndromes, hereditary; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye diseases, hereditary; pseudoxanthoma elasticum Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye diseases, hereditary; pseudoxanthoma elasticum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary thrombophilia. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary thrombophilia. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
optic atrophy, autosomal dominant; optic atrophy, hereditary, leber Gene SetFrom GAD Gene-Disease Associations genes associated with the disease optic atrophy, autosomal dominant; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
optic atrophy, hereditary, leber Gene SetFrom GAD Gene-Disease Associations genes associated with the disease optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary leiomyomatosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary leiomyomatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
optic atrophy, hereditary, leber; vision disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease optic atrophy, hereditary, leber; vision disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary protein c deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary protein c deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
spastic paraplegia, hereditary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease spastic paraplegia, hereditary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary multiple exostoses Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary multiple exostoses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary hemolytic anemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary hemolytic anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infantile-onset ascending hereditary spastic paralysis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infantile-onset ascending hereditary spastic paralysis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary hemorrhagic telangiectasia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary hemorrhagic telangiectasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
corneal dystrophies, hereditary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease corneal dystrophies, hereditary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
type ii hereditary angio-oedema Gene SetFrom GAD Gene-Disease Associations genes associated with the disease type ii hereditary angio-oedema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amyotrophic lateral sclerosis; spastic paraplegia, hereditary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amyotrophic lateral sclerosis; spastic paraplegia, hereditary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary sensory and autonomic neuropathies Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary sensory and autonomic neuropathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term hereditary in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Hereditary Sensory and Motor Neuropathy Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hereditary Sensory and Motor Neuropathy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hyperbilirubinemia, Hereditary Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hyperbilirubinemia, Hereditary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hereditary Motor and Sensory Neuropathies Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hereditary Motor and Sensory Neuropathies phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Elliptocytosis, Hereditary Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Elliptocytosis, Hereditary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Optic Atrophies, Hereditary Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Atrophies, Hereditary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Exostoses, Multiple Hereditary Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Exostoses, Multiple Hereditary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Angioedemas, Hereditary Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Angioedemas, Hereditary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hereditary Autoinflammatory Diseases Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hereditary Autoinflammatory Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Optic Atrophy, Hereditary, Leber Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Atrophy, Hereditary, Leber phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Telangiectasia, Hereditary Hemorrhagic Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Telangiectasia, Hereditary Hemorrhagic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Spherocytosis, Hereditary Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Spherocytosis, Hereditary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Neoplastic Syndromes, Hereditary Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Neoplastic Syndromes, Hereditary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Spastic Paraplegia, Hereditary Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Spastic Paraplegia, Hereditary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hereditary Central Nervous System Demyelinating Diseases Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hereditary Central Nervous System Demyelinating Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Corneal Dystrophies, Hereditary Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Corneal Dystrophies, Hereditary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Nephritis, Hereditary Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Nephritis, Hereditary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hereditary Sensory and Autonomic Neuropathies Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hereditary Sensory and Autonomic Neuropathies phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
chorea, hereditary benign Gene SetFrom OMIM Gene-Disease Associations genes associated with the chorea, hereditary benign phenotype from the curated OMIM Gene-Disease Associations dataset. |
juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuronopathy, distal hereditary motor, type vi Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuronopathy, distal hereditary motor, type vi phenotype from the curated OMIM Gene-Disease Associations dataset. |
ptosis, hereditary congenital, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ptosis, hereditary congenital, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
angioedema, hereditary, type iii Gene SetFrom OMIM Gene-Disease Associations genes associated with the angioedema, hereditary, type iii phenotype from the curated OMIM Gene-Disease Associations dataset. |
angioedema, hereditary, types i and ii Gene SetFrom OMIM Gene-Disease Associations genes associated with the angioedema, hereditary, types i and ii phenotype from the curated OMIM Gene-Disease Associations dataset. |
lymphedema, hereditary, ia Gene SetFrom OMIM Gene-Disease Associations genes associated with the lymphedema, hereditary, ia phenotype from the curated OMIM Gene-Disease Associations dataset. |
lymphedema, hereditary, ib Gene SetFrom OMIM Gene-Disease Associations genes associated with the lymphedema, hereditary, ib phenotype from the curated OMIM Gene-Disease Associations dataset. |
lymphedema, hereditary, ic Gene SetFrom OMIM Gene-Disease Associations genes associated with the lymphedema, hereditary, ic phenotype from the curated OMIM Gene-Disease Associations dataset. |
lymphedema, hereditary, id Gene SetFrom OMIM Gene-Disease Associations genes associated with the lymphedema, hereditary, id phenotype from the curated OMIM Gene-Disease Associations dataset. |
?neuropathy, hereditary sensory and autonomic, type vi Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?neuropathy, hereditary sensory and autonomic, type vi phenotype from the curated OMIM Gene-Disease Associations dataset. |
?neutrophilia, hereditary Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?neutrophilia, hereditary phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, hereditary sensory, with spastic paraplegia Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory, with spastic paraplegia phenotype from the curated OMIM Gene-Disease Associations dataset. |
leukoencephalopathy, diffuse hereditary, with spheroids Gene SetFrom OMIM Gene-Disease Associations genes associated with the leukoencephalopathy, diffuse hereditary, with spheroids phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, hereditary sensory and autonomic, type ia Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory and autonomic, type ia phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, hereditary sensory and autonomic, type ic Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory and autonomic, type ic phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, hereditary sensory and autonomic, type ii Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory and autonomic, type ii phenotype from the curated OMIM Gene-Disease Associations dataset. |
pancreatitis, hereditary Gene SetFrom OMIM Gene-Disease Associations genes associated with the pancreatitis, hereditary phenotype from the curated OMIM Gene-Disease Associations dataset. |
polyposis syndrome, hereditary mixed, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the polyposis syndrome, hereditary mixed, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuronopathy, distal hereditary motor, type vb Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuronopathy, distal hereditary motor, type vb phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuronopathy, distal hereditary motor, type viia Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuronopathy, distal hereditary motor, type viia phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, hereditary sensory, type iic Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory, type iic phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, hereditary sensory and autonomic, type iib Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory and autonomic, type iib phenotype from the curated OMIM Gene-Disease Associations dataset. |
spherocytosis, hereditary, type 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spherocytosis, hereditary, type 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
tremor, hereditary essential, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the tremor, hereditary essential, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
tremor, hereditary essential, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the tremor, hereditary essential, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
tremor, hereditary essential, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the tremor, hereditary essential, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema Gene SetFrom OMIM Gene-Disease Associations genes associated with the dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema phenotype from the curated OMIM Gene-Disease Associations dataset. |
poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene SetFrom OMIM Gene-Disease Associations genes associated with the poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuronopathy, distal hereditary motor, type iid Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuronopathy, distal hereditary motor, type iid phenotype from the curated OMIM Gene-Disease Associations dataset. |
telangiectasia, hereditary hemorrhagic, type 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the telangiectasia, hereditary hemorrhagic, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps Gene SetFrom OMIM Gene-Disease Associations genes associated with the angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, distal hereditary motor, jerash type Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, jerash type phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy with lactic acidosis, hereditary Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy with lactic acidosis, hereditary phenotype from the curated OMIM Gene-Disease Associations dataset. |
[hereditary persistence of fetal hemoglobin] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [hereditary persistence of fetal hemoglobin] phenotype from the curated OMIM Gene-Disease Associations dataset. |
facial paresis, hereditary congenital, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the facial paresis, hereditary congenital, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyperekplexia, hereditary 1, autosomal dominant or recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyperekplexia, hereditary 1, autosomal dominant or recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
hereditary motor and sensory neuropathy v Gene SetFrom OMIM Gene-Disease Associations genes associated with the hereditary motor and sensory neuropathy v phenotype from the curated OMIM Gene-Disease Associations dataset. |
folate malabsorption, hereditary Gene SetFrom OMIM Gene-Disease Associations genes associated with the folate malabsorption, hereditary phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, hereditary sensory, type ie Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory, type ie phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, hereditary sensory, type id Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory, type id phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, hereditary sensory, type if Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory, type if phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, hereditary sensory, type ib Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory, type ib phenotype from the curated OMIM Gene-Disease Associations dataset. |
?neuronopathy, distal hereditary motor, type iic Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?neuronopathy, distal hereditary motor, type iic phenotype from the curated OMIM Gene-Disease Associations dataset. |
[hypoceruloplasminemia, hereditary] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [hypoceruloplasminemia, hereditary] phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, hereditary motor and sensory, russe type Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary motor and sensory, russe type phenotype from the curated OMIM Gene-Disease Associations dataset. |
hereditary motor and sensory neuropathy, proximal type Gene SetFrom OMIM Gene-Disease Associations genes associated with the hereditary motor and sensory neuropathy, proximal type phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, distal hereditary motor, type va Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type va phenotype from the curated OMIM Gene-Disease Associations dataset. |
hereditary motor and sensory neuropathy, type iic Gene SetFrom OMIM Gene-Disease Associations genes associated with the hereditary motor and sensory neuropathy, type iic phenotype from the curated OMIM Gene-Disease Associations dataset. |
ptosis, hereditary congenital 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ptosis, hereditary congenital 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, hereditary sensory and autonomic, type vii Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory and autonomic, type vii phenotype from the curated OMIM Gene-Disease Associations dataset. |
hereditary motor and sensory neuropathy vi Gene SetFrom OMIM Gene-Disease Associations genes associated with the hereditary motor and sensory neuropathy vi phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, distal hereditary motor, type viib Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type viib phenotype from the curated OMIM Gene-Disease Associations dataset. |
telangiectasia, hereditary hemorrhagic, type 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the telangiectasia, hereditary hemorrhagic, type 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
telangiectasia, hereditary hemorrhagic, type 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the telangiectasia, hereditary hemorrhagic, type 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
telangiectasia, hereditary hemorrhagic, type 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the telangiectasia, hereditary hemorrhagic, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
telangiectasia, hereditary hemorrhagic, type 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the telangiectasia, hereditary hemorrhagic, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
dyskeratosis, hereditary benign intraepithelial Gene SetFrom OMIM Gene-Disease Associations genes associated with the dyskeratosis, hereditary benign intraepithelial phenotype from the curated OMIM Gene-Disease Associations dataset. |
hereditary persistence of fetal hemoglobin Gene SetFrom OMIM Gene-Disease Associations genes associated with the hereditary persistence of fetal hemoglobin phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, hereditary sensory and autonomic, type v Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory and autonomic, type v phenotype from the curated OMIM Gene-Disease Associations dataset. |
desmoid disease, hereditary Gene SetFrom OMIM Gene-Disease Associations genes associated with the desmoid disease, hereditary phenotype from the curated OMIM Gene-Disease Associations dataset. |
amyloidosis, hereditary, transthyretin-related Gene SetFrom OMIM Gene-Disease Associations genes associated with the amyloidosis, hereditary, transthyretin-related phenotype from the curated OMIM Gene-Disease Associations dataset. |
amyotrophy, hereditary neuralgic Gene SetFrom OMIM Gene-Disease Associations genes associated with the amyotrophy, hereditary neuralgic phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, distal hereditary motor, type iib Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type iib phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, distal hereditary motor, type iia Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type iia phenotype from the curated OMIM Gene-Disease Associations dataset. |
[hereditary persistence of alpha-fetoprotein] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [hereditary persistence of alpha-fetoprotein] phenotype from the curated OMIM Gene-Disease Associations dataset. |
Defective AMN causes hereditary megaloblastic anemia 1 Gene Setproteins participating in the Defective AMN causes hereditary megaloblastic anemia 1 pathway from the Reactome Pathways dataset. |
Defective CUBN causes hereditary megaloblastic anemia 1 Gene Setproteins participating in the Defective CUBN causes hereditary megaloblastic anemia 1 pathway from the Reactome Pathways dataset. |
Defective TCN2 causes hereditary megaloblastic anemia Gene Setproteins participating in the Defective TCN2 causes hereditary megaloblastic anemia pathway from the Reactome Pathways dataset. |
Hereditary Diffuse Leukoencephalopathy With Spheroids Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Diffuse Leukoencephalopathy With Spheroids in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Motor And Sensory Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Motor And Sensory Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Macular Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Hemochromatosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Hemochromatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Spherocytosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Spherocytosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Macular Coloboma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Macular Coloboma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Whispering Dysphonia, Hereditary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Whispering Dysphonia, Hereditary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hyperbilirubinemia, Hereditary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hyperbilirubinemia, Hereditary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Pancreatitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Pancreatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Hereditary Factor Viii Deficiency Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Hereditary Factor Viii Deficiency Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Multiple Exostoses Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Multiple Exostoses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Melanoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Melanoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Nephritis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Nephritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Sensory Autonomic Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Sensory Autonomic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hyperferritinemia, Hereditary, With Congenital Cataracts Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hyperferritinemia, Hereditary, With Congenital Cataracts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Coproporphyria Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Coproporphyria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hmn (Hereditary Motor Neuropathy) Proximal Type I Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hmn (Hereditary Motor Neuropathy) Proximal Type I in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cerebral Amyloid Angiopathy, Hereditary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Amyloid Angiopathy, Hereditary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Gingival Fibromatosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Gingival Fibromatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Hemorrhagic Telagniectasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Hemorrhagic Telagniectasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Hemorrhagic Telangiectasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Hemorrhagic Telangiectasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Benign Hereditary Chorea Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Benign Hereditary Chorea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Autosomal Recessive Hereditary Spastic Paraplegia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Hereditary Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mild Hereditary Factor Viii Deficiency Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mild Hereditary Factor Viii Deficiency Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Sideroblastic Anemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Sideroblastic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Complicated Hereditary Spastic Paraplegia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Complicated Hereditary Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Autosomal Dominant Spastic Paraplegia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Autosomal Dominant Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Fructose Intolerance Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Fructose Intolerance Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Neuroblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Neuroblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Wilms Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Wilms Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Pyropoikilocytosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Pyropoikilocytosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Spastic Paralysis, Infantile Onset Ascending Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Spastic Paralysis, Infantile Onset Ascending in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Prostate Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Prostate Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Disturbances In Tooth Structure, Not Elsewhere Classified In Icd10Cm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Disturbances In Tooth Structure, Not Elsewhere Classified In Icd10Cm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Desmoid Disease, Hereditary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Desmoid Disease, Hereditary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Diffuse Gastric Adenocarcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Diffuse Gastric Adenocarcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Malignant Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Malignant Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Cardiac Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Cardiac Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Systemic Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Systemic Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cerebral Hemorrhage With Amyloidosis, Hereditary, Dutch Type Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Hemorrhage With Amyloidosis, Hereditary, Dutch Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Cerebral Amyloid Angiopathy, Icelandic Type Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Cerebral Amyloid Angiopathy, Icelandic Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Cerebrovascular Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Cerebrovascular Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Liability To Pressure Palsies Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Liability To Pressure Palsies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Persistence Of Fetal Hemoglobin Thalassemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Persistence Of Fetal Hemoglobin Thalassemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Neurodegenerative Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Neurodegenerative Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Albright'S Hereditary Osteodystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Albright'S Hereditary Osteodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Hyperexplexia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Hyperexplexia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Hyperhomocysteinemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Hyperhomocysteinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pure Hereditary Spastic Paraplegia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pure Hereditary Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sensory Neuropathy, Hereditary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sensory Neuropathy, Hereditary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Antithrombin Iii Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Antithrombin Iii Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adrenocortical Carcinoma, Hereditary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adrenocortical Carcinoma, Hereditary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Paraganglioma-Pheochromocytoma Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Paraganglioma-Pheochromocytoma Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Non-Hereditary Clear Cell Renal Cell Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Non-Hereditary Clear Cell Renal Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypophosphatemic Rickets With Hypercalciuria, Hereditary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypophosphatemic Rickets With Hypercalciuria, Hereditary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polyposis Syndrome, Hereditary Mixed, 2 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polyposis Syndrome, Hereditary Mixed, 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Ovarian Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Ovarian Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Motor Neuronopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Motor Neuronopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Angioedema Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Angioedema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Chorea Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Chorea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Renal Cell Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Renal Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dominant Hereditary Optic Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dominant Hereditary Optic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hfe-Associated Hereditary Hemochromatosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hfe-Associated Hereditary Hemochromatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Clear Cell Renal Cell Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Clear Cell Renal Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Anemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenintal Hereditary Endothelial Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenintal Hereditary Endothelial Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Autosomal Dominant Hereditary Pancreatitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Hereditary Pancreatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Benign Telangiectasia (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Benign Telangiectasia (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Nephropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Hereditary Muscular Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hereditary Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Moderate Hereditary Factor Viii Deficiency Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Moderate Hereditary Factor Viii Deficiency Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Orotoic Aciduria Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Orotoic Aciduria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Cystatin C Amyloid Angiopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Cystatin C Amyloid Angiopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Amyotrophy, Hereditary Neuralgic Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Amyotrophy, Hereditary Neuralgic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary X-Linked Recessive Spastic Paraplegia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary X-Linked Recessive Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
X-Linked, Spastic Paraplegia, Hereditary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease X-Linked, Spastic Paraplegia, Hereditary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Hereditary Motor Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Hereditary Motor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Sensory And Autonomic Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Sensory And Autonomic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Sensory Radicular Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Sensory Radicular Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Bundle Branch System Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Bundle Branch System Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Opalescent Dentin (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Opalescent Dentin (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Keratitis, Hereditary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Keratitis, Hereditary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Paraganglioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Paraganglioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Multiple Osteochondromas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Multiple Osteochondromas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Antithrombin Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Antithrombin Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Hypertyrosinemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Hypertyrosinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Poikiloderma, Hereditary Fibrosing, With Tendon Contractures, Myopathy, And Pulmonary Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Poikiloderma, Hereditary Fibrosing, With Tendon Contractures, Myopathy, And Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Glomangioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Glomangioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Papillary Renal Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Papillary Renal Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Edema Of Legs Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Edema Of Legs in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Palmoplantar Keratoderma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Palmoplantar Keratoderma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Myopathy With Early Respiratory Failure Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Myopathy With Early Respiratory Failure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Folate Malabsorption, Hereditary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Folate Malabsorption, Hereditary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Lymphedema Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Lymphedema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Motor And Sensory Neuropathy, Type Iic (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Motor And Sensory Neuropathy, Type Iic (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thrombasthenia-Thrombocytopenia, Hereditary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thrombasthenia-Thrombocytopenia, Hereditary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Peripheral Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Hyperekplexia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Hyperekplexia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ochronosis, Hereditary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ochronosis, Hereditary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Facial Paresis, Hereditary Congenital, 3 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Facial Paresis, Hereditary Congenital, 3 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Facial Paresis, Hereditary, Congenital Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Facial Paresis, Hereditary, Congenital in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Clubbing Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Clubbing in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Marie Unna Hereditary Hypotrichosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Marie Unna Hereditary Hypotrichosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Continuous Muscle Fiber Activity, Hereditary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Continuous Muscle Fiber Activity, Hereditary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dehydrated Hereditary Stomatocytosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dehydrated Hereditary Stomatocytosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Gastrointestinal Stromal Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Gastrointestinal Stromal Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Leukokeratosis, Hereditary Mucosal Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Leukokeratosis, Hereditary Mucosal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Osteolysis, Hereditary, Of Carpal Bones With Or Without Nephropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Osteolysis, Hereditary, Of Carpal Bones With Or Without Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary And Idiopathic Neuropathy, Unspecified Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary And Idiopathic Neuropathy, Unspecified in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Pheochromocytoma And Paraganglioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Pheochromocytoma And Paraganglioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Stomatocytosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Stomatocytosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Amyloid Nephropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Amyloid Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Glucocorticoid Resistance Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Glucocorticoid Resistance in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Prosopagnosia, Hereditary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Prosopagnosia, Hereditary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Vascular Fragility Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Vascular Fragility in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, And Perinatal Edema Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, And Perinatal Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Protein S Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Protein S Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Oculoleptomeningeal Amyloid Angiopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Oculoleptomeningeal Amyloid Angiopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary C1 Esterase Inhibitor Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary C1 Esterase Inhibitor Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Corneal Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Thrombocytopenic Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Thrombocytopenic Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Vascular Retinopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Vascular Retinopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Disturbances In Tooth Structure, Nec In Icd9Cm_2014 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Disturbances In Tooth Structure, Nec In Icd9Cm_2014 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ptosis, Hereditary Congenital 1 (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ptosis, Hereditary Congenital 1 (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alpha-Fetoprotein, Hereditary Persistence Of Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Alpha-Fetoprotein, Hereditary Persistence Of in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hereditary leiomyomatosis and renal cell carcinoma pathway Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Hereditary leiomyomatosis and renal cell carcinoma pathway pathway from the WikiPathways Pathways 2024 dataset. |
Defective SERPING1 causes hereditary angioedema Gene Setproteins participating in the Defective SERPING1 causes hereditary angioedema pathway from the Reactome Pathways 2024 dataset. |
Defective SLC34A3 causes Hereditary hypophosphatemic rickets with hypercalciuria (HHRH) Gene Setproteins participating in the Defective SLC34A3 causes Hereditary hypophosphatemic rickets with hypercalciuria (HHRH) pathway from the Reactome Pathways 2024 dataset. |
Defective SLC4A1 causes hereditary spherocytosis type 4 (HSP4), distal renal tubular acidosis (dRTA) and dRTA with hemolytic anemia (dRTA-HA) Gene Setproteins participating in the Defective SLC4A1 causes hereditary spherocytosis type 4 (HSP4), distal renal tubular acidosis (dRTA) and dRTA with hemolytic anemia (dRTA-HA) pathway from the Reactome Pathways 2024 dataset. |
Defective SLC5A7 causes distal hereditary motor neuronopathy 7A (HMN7A)_5619114 Gene Setproteins participating in the Defective SLC5A7 causes distal hereditary motor neuronopathy 7A (HMN7A)_5619114 pathway from the Reactome Pathways 2024 dataset. |
Defective SLC5A7 causes distal hereditary motor neuronopathy 7A (HMN7A)_5658471 Gene Setproteins participating in the Defective SLC5A7 causes distal hereditary motor neuronopathy 7A (HMN7A)_5658471 pathway from the Reactome Pathways 2024 dataset. |
Defective factor XII causes hereditary angioedema Gene Setproteins participating in the Defective factor XII causes hereditary angioedema pathway from the Reactome Pathways 2024 dataset. |
Hereditary fructose intolerance Gene Setproteins participating in the Hereditary fructose intolerance pathway from the Reactome Pathways 2024 dataset. |
Hereditary spastic paraplegia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Leber hereditary optic neuropathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Leber hereditary optic neuropathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary ataxia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary ataxia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary multiple exostoses Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary multiple exostoses from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary night blindness Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary night blindness from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary elliptocytosis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary elliptocytosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 31 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 31 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant distal hereditary motor neuronopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 5 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant distal hereditary motor neuronopathy 5 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 15 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 15 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary retinal dystrophy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary retinal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary hemorrhagic telangiectasia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary hemorrhagic telangiectasia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary sensory and autonomic neuropathy type 2 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary sensory and autonomic neuropathy type 2 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary sensory neuropathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary sensory neuropathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary angioedema Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary angioedema from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy 1 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal recessive distal hereditary motor neuronopathy 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal recessive distal hereditary motor neuronopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 35 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 35 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary spherocytosis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spherocytosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 2 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 2 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary folate malabsorption Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary folate malabsorption from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 7 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 7 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 3A Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 3A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary neuropathy with liability to pressure palsies Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary neuropathy with liability to pressure palsies from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 5A Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 5A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 8 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 8 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary sensory and autonomic neuropathy type 1 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary sensory and autonomic neuropathy type 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary sensory and autonomic neuropathy type 1A Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary sensory and autonomic neuropathy type 1A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 11 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 11 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary lymphedema I Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary lymphedema I from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary lymphedema Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary lymphedema from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary sensory neuropathy type 1E Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary sensory neuropathy type 1E from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 49 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 49 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 17 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary spastic paraplegia 17 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
X-linked hereditary ataxia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease X-linked hereditary ataxia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary sensory and autonomic neuropathy type 5 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary sensory and autonomic neuropathy type 5 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Leber hereditary optic neuropathy and dystonia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Leber hereditary optic neuropathy and dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary ataxia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Leber hereditary optic neuropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Leber hereditary optic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary night blindness Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary night blindness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary multiple exostoses Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary multiple exostoses in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spherocytosis type 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spherocytosis type 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
X-linked hereditary ataxia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked hereditary ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary sensory neuropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary papulotranslucent acrokeratoderma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary papulotranslucent acrokeratoderma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary arterial and articular multiple calcification syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary arterial and articular multiple calcification syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary angioedema Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary angioedema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary neuropathy with liability to pressure palsies Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary neuropathy with liability to pressure palsies in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary elliptocytosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary elliptocytosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spherocytosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spherocytosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary hemorrhagic telangiectasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary hemorrhagic telangiectasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Dehydrated hereditary stomatocytosis 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dehydrated hereditary stomatocytosis 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Dehydrated hereditary stomatocytosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dehydrated hereditary stomatocytosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 12 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 31 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 31 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 6 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 13 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary renal cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary renal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary sensory and autonomic neuropathy type 2A Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory and autonomic neuropathy type 2A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary sensory and autonomic neuropathy type 1A Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory and autonomic neuropathy type 1A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 16 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 16 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary coproporphyria Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary coproporphyria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 61 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 61 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 73 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 73 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 10 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 28 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 28 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 17 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 17 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 18 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 18 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 39 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 39 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 35 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 35 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 41 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 41 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital hereditary endothelial dystrophy of cornea Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital hereditary endothelial dystrophy of cornea in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary retinal dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary retinal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary folate malabsorption Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary folate malabsorption in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary mixed polyposis syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary mixed polyposis syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 76 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 76 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary lymphedema I Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary lymphedema I in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary lymphedema Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary lymphedema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary hypophosphatemic rickets with hypercalciuria Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary hypophosphatemic rickets with hypercalciuria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary sensory and autonomic neuropathy type 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory and autonomic neuropathy type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 49 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 49 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary sensory and autonomic neuropathy type 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory and autonomic neuropathy type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 54 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 54 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 50 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 50 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary fructose intolerance syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary fructose intolerance syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary choroidal atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary choroidal atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 81 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 81 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 78 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 78 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 42 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 42 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary sensory neuropathy type 2C Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory neuropathy type 2C in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 75 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 75 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary lymphedema II Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary lymphedema II in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spherocytosis type 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spherocytosis type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary sensory neuropathy type 1E Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory neuropathy type 1E in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary combined deficiency of vitamin K-dependent clotting factors Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary combined deficiency of vitamin K-dependent clotting factors in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Albright's hereditary osteodystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Albright's hereditary osteodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spherocytosis type 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spherocytosis type 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 15 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 15 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary desmoid disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary desmoid disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spherocytosis type 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spherocytosis type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary Wilms' tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary Wilms' tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 14 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary sensory and autonomic neuropathy type 6 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory and autonomic neuropathy type 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 55 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 55 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 9A Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 9A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 23 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 23 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary sensory and autonomic neuropathy type 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory and autonomic neuropathy type 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary sensory and autonomic neuropathy type 1C Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory and autonomic neuropathy type 1C in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Juvenile polyposis-hereditary hemorrhagic telangiectasia syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Juvenile polyposis-hereditary hemorrhagic telangiectasia syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 44 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 44 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary sensory and autonomic neuropathy type 2B Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory and autonomic neuropathy type 2B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 11 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 7 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 27 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 27 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 36 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 36 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 30 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 30 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 26 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 26 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 63 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 63 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 45 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 45 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 43 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 43 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 37 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 37 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 56 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 56 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 46 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 46 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 77 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 77 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 70 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 70 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 5A Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 5A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 8 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 64 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 64 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary neutrophilia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary neutrophilia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary angioedema type I Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary angioedema type I in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 9 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary alpha tryptasemia syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary alpha tryptasemia syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 7 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 47 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 47 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 3A Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 3A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 6 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 8 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 52 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 52 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary sensory neuropathy type 1D Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory neuropathy type 1D in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary sensory and autonomic neuropathy type 8 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory and autonomic neuropathy type 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary sensory neuropathy type 1B Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory neuropathy type 1B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary sensory and autonomic neuropathy type 7 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory and autonomic neuropathy type 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary sensory neuropathy type 1F Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory neuropathy type 1F in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary mixed polyposis syndrome 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary mixed polyposis syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 84 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 84 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 57 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 57 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary angioedema type III Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary angioedema type III in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 48 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 48 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Overhydrated hereditary stomatocytosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Overhydrated hereditary stomatocytosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 32 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 32 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 19 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 19 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary lymphedema IA Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary lymphedema IA in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 38 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 38 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 51 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 51 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spherocytosis type 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spherocytosis type 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy 8 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary lymphedema IC Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary lymphedema IC in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 72A Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 72A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 14 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 25 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 25 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary mixed polyposis syndrome 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary mixed polyposis syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 87 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 87 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 9B Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 9B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Dehydrated hereditary stomatocytosis 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dehydrated hereditary stomatocytosis 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 82 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 82 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary spastic paraplegia 29 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary spastic paraplegia 29 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary sensory neuropathy type 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory neuropathy type 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary conventional renal cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary conventional renal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |