Name

Telangiectasia, Hereditary Hemorrhagic Gene Set

From CTD Gene-Disease Associations

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

telangiectasia, hereditary hemorrhagic Gene Set

From 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.

Telangiectasia, Hereditary Hemorrhagic Gene Set

From 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.

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

From GAD Gene-Disease Associations

genes associated with the disease gastrointestinal neoplasms; hht - hereditary hemorrhagic telangiectasia; intestinal polyposis; neoplastic syndromes, hereditary; telangiectasia, hereditary hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Pulmonary hypertension, primary, 1, with hereditary hemorrhagic telangiectasia Gene Set

From 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.

Telangiectasia, hereditary hemorrhagic, type 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Telangiectasia, hereditary hemorrhagic, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary hemorrhagic telangiectasia type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary hemorrhagic telangiectasia type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pulmonary arterial hypertension related to hereditary hemorrhagic telangiectasia Gene Set

From 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.

Hereditary hemorrhagic telangiectasia type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary hemorrhagic telangiectasia type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Juvenile Polyposis with Hereditary Hemorrhagic Telangiectasia Gene Set

From CTD Gene-Disease Associations

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

Telangiectasia, Hereditary Hemorrhagic, Type 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Telangiectasia, Hereditary Hemorrhagic, Type 4 from the curated CTD Gene-Disease Associations dataset.

hereditary hemorrhagic telangiectasia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

hereditary hemorrhagic telangiectasia Gene Set

From DISEASES Text-mining Gene-Disease Assocation 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.

hemorrhagic telangiectasia, hereditary Gene Set

From 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.

arteriovenous malformations; liver diseases; telangiectasia, hereditary hemorrhagic Gene Set

From 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.

heart diseases; hyperplasia; liver diseases; telangiectasia, hereditary hemorrhagic Gene Set

From 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.

hereditary hemorrhagic telangiectasia Gene Set

From 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.

juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome Gene Set

From OMIM Gene-Disease Associations

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

telangiectasia, hereditary hemorrhagic, type 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the telangiectasia, hereditary hemorrhagic, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

telangiectasia, hereditary hemorrhagic, type 4 Gene Set

From 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 Set

From 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 Set

From 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 Set

From OMIM Gene-Disease Associations

genes associated with the telangiectasia, hereditary hemorrhagic, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

Osler hemorrhagic telangiectasia syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osler hemorrhagic telangiectasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

eye diseases, hereditary; hearing impairment; hearing loss; hereditary nephritis; nephritis, hereditary Gene Set

From 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.

Telangiectasia, Hereditary Benign Gene Set

From CTD Gene-Disease Associations

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

Hereditary cancer-predisposing syndrome:Hereditary cancer-predisposing syndrome Gene Set

From 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 Set

From 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.

colorectal neoplasms, hereditary nonpolyposis; hereditary nonpolyposis colorectal neoplasms; neoplasms Gene Set

From 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.

charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy Gene Set

From 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.

colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms; hereditary nonpolyposis colorectal neoplasms Gene Set

From 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.

corneal dystrophies, hereditary; hereditary corneal dystrophy Gene Set

From 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.

colorectal neoplasms, hereditary nonpolyposis; hereditary nonpolyposis colorectal neoplasms; neoplasms, second primary; rectal neoplasms Gene Set

From 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 Set

From 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 Set

From 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 nephritis; nephritis, hereditary Gene Set

From 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 Set

From 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 Set

From 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.

Ataxia-telangiectasia-like disorder Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ataxia-telangiectasia-like disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ataxia-telangiectasia syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ataxia-telangiectasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypotrichosis-lymphedema-telangiectasia syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypotrichosis-lymphedema-telangiectasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Haemorrhagic telangiectasia 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Haemorrhagic telangiectasia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ataxia-telangiectasia-like disorder 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ataxia-telangiectasia-like disorder 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Haemorrhagic telangiectasia 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Haemorrhagic telangiectasia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ataxia-telangiectasia variant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ataxia-telangiectasia variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cutaneous telangiectasia and cancer syndrome, familial Gene Set

From ClinVar Gene-Phenotype Associations

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

Ataxia Telangiectasia Gene Set

From CTD Gene-Disease Associations

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

ATAXIA-TELANGIECTASIA-LIKE DISORDER 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ATAXIA-TELANGIECTASIA-LIKE DISORDER 1 from the curated CTD Gene-Disease Associations dataset.

Hypotrichosis-Lymphedema-Telangiectasia Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypotrichosis-Lymphedema-Telangiectasia Syndrome from the curated CTD Gene-Disease Associations dataset.

ataxia telangiectasia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

retinal telangiectasia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

ataxia telangiectasia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

ataxia telangiectasia Gene Set

From GAD Gene-Disease Associations

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

radiation-induced ocular telangiectasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease radiation-induced ocular telangiectasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ataxia telangiectasia; louis-bar syndrome; lymphoma, non-hodgkin; lymphoma, non-hodgkin's Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ataxia telangiectasia; louis-bar syndrome; lymphoma, non-hodgkin; lymphoma, non-hodgkin's in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ataxia-telangiectasia Gene Set

From GAD Gene-Disease Associations

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

ataxia telangiectasia; fragile x syndrome; tremor Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ataxia telangiectasia; fragile x syndrome; tremor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ataxia telangiectasia; neoplasms Gene Set

From GAD Gene-Disease Associations

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

ataxia telangiectasia; carcinoma, squamous cell; mouth neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ataxia telangiectasia; carcinoma, squamous cell; mouth neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

telangiectasia Gene Set

From GeneRIF Biological Term Annotations

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

telangiectasia macularis eruptiva perstans Gene Set

From HPO Gene-Disease Associations

genes associated with the telangiectasia macularis eruptiva perstans phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

telangiectasia of the oral mucosa Gene Set

From HPO Gene-Disease Associations

genes associated with the telangiectasia of the oral mucosa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

retinal telangiectasia Gene Set

From HPO Gene-Disease Associations

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

nasal mucosa telangiectasia Gene Set

From HPO Gene-Disease Associations

genes associated with the nasal mucosa telangiectasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

gastrointestinal telangiectasia Gene Set

From HPO Gene-Disease Associations

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

facial telangiectasia in butterfly midface distribution Gene Set

From HPO Gene-Disease Associations

genes associated with the facial telangiectasia in butterfly midface distribution phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

telangiectasia Gene Set

From HPO Gene-Disease Associations

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

facial telangiectasia Gene Set

From HPO Gene-Disease Associations

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

tongue telangiectasia Gene Set

From HPO Gene-Disease Associations

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

lip telangiectasia Gene Set

From HPO Gene-Disease Associations

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

palmar telangiectasia Gene Set

From HPO Gene-Disease Associations

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

palate telangiectasia Gene Set

From HPO Gene-Disease Associations

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

nail bed telangiectasia Gene Set

From HPO Gene-Disease Associations

genes associated with the nail bed telangiectasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

diffuse telangiectasia Gene Set

From HPO Gene-Disease Associations

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

conjunctival telangiectasia Gene Set

From HPO Gene-Disease Associations

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

Ataxia Telangiectasia Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

hypotrichosis-lymphedema-telangiectasia syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypotrichosis-lymphedema-telangiectasia syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

ataxia-telangiectasia-like disorder Gene Set

From OMIM Gene-Disease Associations

genes associated with the ataxia-telangiectasia-like disorder phenotype from the curated OMIM Gene-Disease Associations dataset.

ataxia-telangiectasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the ataxia-telangiectasia phenotype from the curated OMIM Gene-Disease Associations dataset.

?ataxia-telangiectasia-like disorder Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?ataxia-telangiectasia-like disorder phenotype from the curated OMIM Gene-Disease Associations dataset.

cutaneous telangiectasia and cancer syndrome, familial Gene Set

From OMIM Gene-Disease Associations

genes associated with the cutaneous telangiectasia and cancer syndrome, familial phenotype from the curated OMIM Gene-Disease Associations dataset.

telangiectasia Gene Set

From Phosphosite Textmining Biological Term Annotations

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

ataxia-telangiectasia Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease ataxia-telangiectasia from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

Hemorrhagic destruction of the brain, subependymal calcification, and cataracts Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemorrhagic destruction of the brain, subependymal calcification, and cataracts phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Darier disease, acral hemorrhagic type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Darier disease, acral hemorrhagic type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemorrhagic Disorders Gene Set

From CTD Gene-Disease Associations

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

Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells from the curated CTD Gene-Disease Associations dataset.

Shock, Hemorrhagic Gene Set

From CTD Gene-Disease Associations

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

HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION, AND CATARACTS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION, AND CATARACTS from the curated CTD Gene-Disease Associations dataset.

Dengue Hemorrhagic Fever Gene Set

From dbGAP Gene-Trait Associations

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

hemorrhagic thrombocythemia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

hemorrhagic disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

hemorrhagic disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

venezuelan hemorrhagic fever Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

bolivian hemorrhagic fever Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hemorrhagic disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

ebola hemorrhagic fever Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

acute hemorrhagic leukoencephalitis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

crimean-congo hemorrhagic fever Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

argentine hemorrhagic fever Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hemorrhagic thrombocythemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

marburg hemorrhagic fever Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

acute hemorrhagic conjunctivitis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

dengue hemorrhagic fever Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

korean hemorrhagic fever Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

vitamin k deficiency hemorrhagic disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hemorrhagic fever with renal syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

dengue hemorrhagic fever Gene Set

From GAD Gene-Disease Associations

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

polycythemia vera; thrombocythemia, essential; thrombocythemia, hemorrhagic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycythemia vera; thrombocythemia, essential; thrombocythemia, hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemorrhage; hemorrhagic disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hemorrhage; hemorrhagic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myeloproliferative disorders; thrombocythemia, essential; thrombocythemia, hemorrhagic; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myeloproliferative disorders; thrombocythemia, essential; thrombocythemia, hemorrhagic; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myeloproliferative disorders; polycythemia vera; thrombocythemia, essential; thrombocythemia, hemorrhagic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myeloproliferative disorders; polycythemia vera; thrombocythemia, essential; thrombocythemia, hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dengue; dengue hemorrhagic fever; thrombocytopenia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dengue; dengue hemorrhagic fever; thrombocytopenia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neovascularization, pathologic; polycythemia vera; thrombocythemia, essential; thrombocythemia, hemorrhagic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neovascularization, pathologic; polycythemia vera; thrombocythemia, essential; thrombocythemia, hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemorrhagic disorders Gene Set

From GAD Gene-Disease Associations

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

myeloproliferative disorders; philadelphia chromosome; polycythemia vera; primary myelofibrosis; thrombocythemia, essential; thrombocythemia, hemorrhagic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myeloproliferative disorders; philadelphia chromosome; polycythemia vera; primary myelofibrosis; thrombocythemia, essential; thrombocythemia, hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polycythemia vera; thrombocythemia, hemorrhagic; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycythemia vera; thrombocythemia, hemorrhagic; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemorrhagic fever, crimean Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hemorrhagic fever, crimean in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemorrhagic fever with renal syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hemorrhagic fever with renal syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dengue; dengue fever; dengue hemorrhagic fever Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dengue; dengue fever; dengue hemorrhagic fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemorrhagic and ischemic stroke Gene Set

From GAD Gene-Disease Associations

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

hemorrhagic stroke Gene Set

From GAD Gene-Disease Associations

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

leucocytosis; leukocytosis; thrombocythemia, hemorrhagic; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leucocytosis; leukocytosis; thrombocythemia, hemorrhagic; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dengue hemorrhagic fever; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dengue hemorrhagic fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; cardiovascular diseases; polycythemia vera; recurrence; thrombocythemia, hemorrhagic; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; cardiovascular diseases; polycythemia vera; recurrence; thrombocythemia, hemorrhagic; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemorrhagic fever, ebola Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hemorrhagic fever, ebola in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blast crisis; blast phase; polycythemia vera; primary myelofibrosis; thrombocythemia, essential; thrombocythemia, hemorrhagic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blast crisis; blast phase; polycythemia vera; primary myelofibrosis; thrombocythemia, essential; thrombocythemia, hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

stroke, ischemic; stroke, hemorrhagic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease stroke, ischemic; stroke, hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemorrhagic fever with renal syndrome; pleural effusion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hemorrhagic fever with renal syndrome; pleural effusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

primary myelofibrosis; thrombocythemia, essential; thrombocythemia, hemorrhagic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease primary myelofibrosis; thrombocythemia, essential; thrombocythemia, hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

stroke, hemorrhagic Gene Set

From GAD Gene-Disease Associations

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

hematologic diseases; hematologic neoplasms; leukemia, myeloid; myeloid leukemia; thrombocythemia, hemorrhagic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hematologic diseases; hematologic neoplasms; leukemia, myeloid; myeloid leukemia; thrombocythemia, hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid; myeloid leukemia; thrombocythemia, essential; thrombocythemia, hemorrhagic; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid; myeloid leukemia; thrombocythemia, essential; thrombocythemia, hemorrhagic; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemorrhagic Gene Set

From GeneRIF Biological Term Annotations

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

hemorrhagic thrombocythemia Gene Set

From GWASdb SNP-Disease Associations

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

hemorrhagic disease Gene Set

From GWASdb SNP-Disease Associations

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

Hemorrhagic Septicemia Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Hemorrhagic Disorders Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Dengue Hemorrhagic Fever Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Dengue Hemorrhagic Fever phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Hemorrhagic Fever, Ebola Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hemorrhagic Fever, Ebola phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Hemorrhagic Fever, Crimean Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hemorrhagic Fever, Crimean phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Thrombocythemia, Hemorrhagic Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Thrombocythemia, Hemorrhagic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Hemorrhagic Fever with Renal Syndrome Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hemorrhagic Fever with Renal Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Hemorrhagic Disease of Newborn Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hemorrhagic Disease of Newborn phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Leukoencephalitis, Acute Hemorrhagic Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Leukoencephalitis, Acute Hemorrhagic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

hemorrhagic ascites Gene Set

From MPO Gene-Phenotype Associations

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

hemorrhagic destruction of the brain, subependymal calcification, and cataracts Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemorrhagic destruction of the brain, subependymal calcification, and cataracts phenotype from the curated OMIM Gene-Disease Associations dataset.

hemorrhagic diathesis due to 'antithrombin' pittsburgh Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemorrhagic diathesis due to 'antithrombin' pittsburgh phenotype from the curated OMIM Gene-Disease Associations dataset.

{stroke, hemorrhagic} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {stroke, hemorrhagic} phenotype from the curated OMIM Gene-Disease Associations dataset.

Hereditary acrodermatitis enteropathica Gene Set

From 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 Set

From 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 Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary liability to pressure palsies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Prostate cancer, hereditary, 13 Gene Set

From 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 Set

From 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 Set

From 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 neutrophilia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary neutrophilia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary cancer-predisposing syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Facial paresis, hereditary congenital, 3 Gene Set

From 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 Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary sideroblastic anemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary hemochromatosis Gene Set

From 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 Set

From 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 Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neuropathy hereditary sensory and autonomic type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary fructosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary neuralgic amyotrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary neuralgic amyotrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Von Hippel-Lindau syndrome:Hereditary cancer-predisposing syndrome Gene Set

From 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.

Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant Gene Set

From 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.

Lynch syndrome:Hereditary cancer-predisposing syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lynch syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neuropathy, hereditary motor and sensory, Okinawa type Gene Set

From 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 Set

From 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 Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary factor II deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary diffuse gastric cancer Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary diffuse gastric cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY, TYPE IE Gene Set

From 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 Set

From 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 Set

From 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 Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alpha-fetoprotein, hereditary persistence of phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Prostate cancer, hereditary, 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Prostate cancer, hereditary, 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary lymphedema type I Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lymphedema, hereditary, ic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lymphedema, hereditary, id Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 leiomyomatosis and renal cell cancer Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary leiomyomatosis and renal cell cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary angioedema type 1 Gene Set

From 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 Set

From 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 Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary pyropoikilocytosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary cancer-predisposing syndrome:Peutz-Jeghers syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary cancer-predisposing syndrome:Peutz-Jeghers syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Distal hereditary motor neuronopathy type 7B Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

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

From ClinVar Gene-Phenotype Associations

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

Distal hereditary motor neuronopathy type 5 Gene Set

From 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 Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Prostate cancer, hereditary, 1 Gene Set

From 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 Set

From ClinVar Gene-Phenotype Associations

genes associated with the Prostate cancer, hereditary, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary pancreatitis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary pancreatitis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary factor VIII deficiency disease Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary cerebral amyloid angiopathy, Icelandic type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary nonpolyposis colorectal cancer type 5 Gene Set

From 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 Set

From 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 Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary nonpolyposis colorectal cancer type 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Prostate Cancer, Hereditary, 15 Gene Set

From 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 Set

From 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 Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Prostate Cancer, Hereditary, 8 from the curated CTD Gene-Disease Associations dataset.

Hereditary renal agenesis Gene Set

From 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 Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dyskeratosis, Hereditary Benign Intraepithelial from the curated CTD Gene-Disease Associations dataset.

Prostate Cancer, Hereditary, 14 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Prostate Cancer, Hereditary, 14 from the curated CTD Gene-Disease Associations dataset.

Tremor hereditary essential, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Tremor hereditary essential, 1 from the curated CTD Gene-Disease Associations dataset.

Prostate Cancer, Hereditary, 11 Gene Set

From 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 Set

From 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 Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Prostate Cancer, Hereditary, 12 from the curated CTD Gene-Disease Associations dataset.

Hereditary Sensory and Motor Neuropathy Gene Set

From 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 Set

From CTD Gene-Disease Associations

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

Angioedemas, Hereditary Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From CTD Gene-Disease Associations

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

Elliptocytosis, Hereditary Gene Set

From 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 Set

From 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 Set

From CTD Gene-Disease Associations

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

PROSTATE CANCER, HEREDITARY, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PROSTATE CANCER, HEREDITARY, 1 from the curated CTD Gene-Disease Associations dataset.

Neuropathy, hereditary motor and sensory, Russe type Gene Set

From 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 Set

From 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 Set

From 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 Set

From CTD Gene-Disease Associations

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

Prostate Cancer, Hereditary, 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Prostate Cancer, Hereditary, 10 from the curated CTD Gene-Disease Associations dataset.

Neuropathy, Distal Hereditary Motor, Type IIA Gene Set

From 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 Set

From 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 Set

From 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 Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Folate Malabsorption, Hereditary from the curated CTD Gene-Disease Associations dataset.

HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER from the curated CTD Gene-Disease Associations dataset.

Bullous Dystrophy, Hereditary Macular Type Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic Atrophies, Hereditary from the curated CTD Gene-Disease Associations dataset.

Neuronopathy, Distal Hereditary Motor, Type V Gene Set

From 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 Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Exostoses, Multiple Hereditary from the curated CTD Gene-Disease Associations dataset.

Prostate Cancer, Hereditary, X-Linked 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Prostate Cancer, Hereditary, X-Linked 2 from the curated CTD Gene-Disease Associations dataset.

Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From CTD Gene-Disease Associations

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

Hereditary Breast and Ovarian Cancer Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hereditary Breast and Ovarian Cancer Syndrome from the curated CTD Gene-Disease Associations dataset.

Ptosis, Hereditary Congenital 2 Gene Set

From 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 Set

From 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 Set

From 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 Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hereditary Myopathy with Early Respiratory Failure from the curated CTD Gene-Disease Associations dataset.

Colorectal Cancer, Hereditary Nonpolyposis, Type 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Colorectal Cancer, Hereditary Nonpolyposis, Type 8 from the curated CTD Gene-Disease Associations dataset.

NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC Gene Set

From 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 Set

From 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.

Prostate Cancer, Hereditary, 5 Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Prostate Cancer, Hereditary, 3 from the curated CTD Gene-Disease Associations dataset.

Coproporphyria, Hereditary Gene Set

From CTD Gene-Disease Associations

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

PROSTATE CANCER, HEREDITARY, X-LINKED 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PROSTATE CANCER, HEREDITARY, X-LINKED 1 from the curated CTD Gene-Disease Associations dataset.

Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive Gene Set

From 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 Set

From 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 Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, Distal Hereditary Motor, Type VIIA from the curated CTD Gene-Disease Associations dataset.

Keratitis, hereditary Gene Set

From 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 Set

From 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 Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy with Lactic Acidosis, Hereditary from the curated CTD Gene-Disease Associations dataset.

Colorectal Neoplasms, Hereditary Nonpolyposis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Colorectal Neoplasms, Hereditary Nonpolyposis from the curated CTD Gene-Disease Associations dataset.

Leukokeratosis, Hereditary Mucosal Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From CTD Gene-Disease Associations

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

Nephritis, Hereditary Gene Set

From 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 Set

From 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 Set

From CTD Gene-Disease Associations

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

Corneal Dystrophies, Hereditary Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophies, Hereditary from the curated CTD Gene-Disease Associations dataset.

hereditary spherocytosis Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

hereditary spastic paraplegia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

hereditary elliptocytosis Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

hereditary angioedema Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

hereditary sensory neuropathy Gene Set

From DISEASES Curated Gene-Disease Assocation 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 Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease hereditary fructose intolerance syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

hereditary lymphedema Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

hereditary mucosal leukokeratosis Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

hereditary multiple exostoses Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

hereditary sensory neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 spastic paraplegia Gene Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 breast ovarian cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation 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 coproporphyria Gene Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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.

colonic neoplasms; colorectal neoplasms, hereditary nonpolyposis; microsatellite instability Gene Set

From 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 Set

From 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 Set

From 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.

corneal dystrophies, hereditary; Gene Set

From 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.

anticipation, genetic; colorectal neoplasms, hereditary nonpolyposis Gene Set

From 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.

leber's hereditary optic neuropathy Gene Set

From 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 Set

From 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.

hereditary and sporadic prostate cancer risk. Gene Set

From 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.

hyperbilirubinemia, hereditary Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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.

colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; recurrence Gene Set

From 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.

hereditary hemochromatosis in african americans. Gene Set

From 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.

hereditary spastic paraparesis due to a frame shift mutat Gene Set

From 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 Set

From 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 Set

From 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.

colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; genital neoplasms, female; neoplasms Gene Set

From 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.

hereditary hemochromatosis. Gene Set

From 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 Set

From 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 Set

From 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.

hereditary nonpolyposis colon cancer. Gene Set

From 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.

blindness; optic atrophy, hereditary, leber Gene Set

From 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.

breast neoplasms; colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms; Gene Set

From 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.

hereditary autoinflammatory diseases; lymphadenitis; pharyngitis; stomatitis, aphthous; syndrome Gene Set

From 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.

colorectal cancer, hereditary nonpolyposis Gene Set

From 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.

hereditary haemolytic anaemia. Gene Set

From 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.

hereditary non-polyposis colon cancer. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hereditary non-polyposis colon cancer. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic kidney diseases; kidney diseases, cystic; leber congenital amaurosis; optic atrophies, hereditary; vision disorders Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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.

colorectal neoplasms, hereditary nonpolyposis; pancreatic neoplasms Gene Set

From 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 Set

From 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.

hereditary dementia. Gene Set

From 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.

charcot-marie-tooth disease; hereditary sensory and motor neuropathy Gene Set

From 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.

breast neoplasms; neoplastic syndromes, hereditary; ovarian neoplasms Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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.

colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms Gene Set

From 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.

optic atrophy, hereditary, leber Gene Set

From 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 Set

From 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.

adenocarcinoma; colonic neoplasms; colorectal neoplasms, hereditary nonpolyposis; microsatellite instability Gene Set

From 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.

optic atrophy, hereditary, leber; vision disorders Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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.

colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis Gene Set

From 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.

hereditary and sporadic prostate cancer susceptibility. Gene Set

From 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.

corneal dystrophies, hereditary Gene Set

From 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.

adenocarcinoma; colorectal neoplasms, hereditary nonpolyposis; microsatellite instability Gene Set

From 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 Set

From 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.

type ii hereditary angio-oedema Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 nonpolyposis colorectal carcinoma Gene Set

From 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.

Hereditary Sensory and Motor Neuropathy Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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.

Spherocytosis, Hereditary Gene Set

From 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.

Colorectal Neoplasms, Hereditary Nonpolyposis Gene Set

From 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.

Neoplastic Syndromes, Hereditary Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From OMIM Gene-Disease Associations

genes associated with the chorea, hereditary benign phenotype from the curated OMIM Gene-Disease Associations dataset.

{prostate cancer, hereditary, 7} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {prostate cancer, hereditary, 7} phenotype from the curated OMIM Gene-Disease Associations dataset.

neuronopathy, distal hereditary motor, type vi Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From OMIM Gene-Disease Associations

genes associated with the lymphedema, hereditary, ia phenotype from the curated OMIM Gene-Disease Associations dataset.

lymphedema, hereditary, ib Gene Set

From OMIM Gene-Disease Associations

genes associated with the lymphedema, hereditary, ib phenotype from the curated OMIM Gene-Disease Associations dataset.

lymphedema, hereditary, ic Gene Set

From OMIM Gene-Disease Associations

genes associated with the lymphedema, hereditary, ic phenotype from the curated OMIM Gene-Disease Associations dataset.

lymphedema, hereditary, id Gene Set

From 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 Set

From OMIM Gene-Disease Associations

genes associated with the ?neuropathy, hereditary sensory and autonomic, type vi phenotype from the curated OMIM Gene-Disease Associations dataset.

{prostate cancer, hereditary, 2, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {prostate cancer, hereditary, 2, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

?neutrophilia, hereditary Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, hereditary sensory and autonomic, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

colorectal cancer, hereditary nonpolyposis, type 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the colorectal cancer, hereditary nonpolyposis, type 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

pancreatitis, hereditary Gene Set

From 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 Set

From OMIM Gene-Disease Associations

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

colorectal cancer, hereditary nonpolyposis, type 8 Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From OMIM Gene-Disease Associations

genes associated with the colorectal cancer, hereditary nonpolyposis, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

neuronopathy, distal hereditary motor, type vb Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From OMIM Gene-Disease Associations

genes associated with the spherocytosis, hereditary, type 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

{prostate cancer, hereditary, 9} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {prostate cancer, hereditary, 9} phenotype from the curated OMIM Gene-Disease Associations dataset.

tremor, hereditary essential, 3 Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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.

{prostate cancer, hereditary, 12} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {prostate cancer, hereditary, 12} phenotype from the curated OMIM Gene-Disease Associations dataset.

poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene Set

From 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 Set

From OMIM Gene-Disease Associations

genes associated with the neuronopathy, distal hereditary motor, type iid phenotype from the curated OMIM Gene-Disease Associations dataset.

{prostate cancer, hereditary, 10} Gene Set

From 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 Set

From OMIM Gene-Disease Associations

genes associated with the prostate cancer, hereditary phenotype from the curated OMIM Gene-Disease Associations dataset.

angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From OMIM Gene-Disease Associations

genes associated with the [hypoceruloplasminemia, hereditary] phenotype from the curated OMIM Gene-Disease Associations dataset.

{prostate cancer, hereditary, 14} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {prostate cancer, hereditary, 14} phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, hereditary motor and sensory, russe type Gene Set

From 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 Set

From 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 Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, distal hereditary motor, type va phenotype from the curated OMIM Gene-Disease Associations dataset.

{prostate cancer, hereditary, x-linked 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {prostate cancer, hereditary, x-linked 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

hereditary motor and sensory neuropathy, type iic Gene Set

From 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 Set

From OMIM Gene-Disease Associations

genes associated with the ptosis, hereditary congenital 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

{prostate cancer, hereditary, 15} Gene Set

From 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 Set

From OMIM Gene-Disease Associations

genes associated with the {prostate cancer, hereditary, 13} phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, hereditary sensory and autonomic, type vii Gene Set

From 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 Set

From 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 Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, distal hereditary motor, type viib phenotype from the curated OMIM Gene-Disease Associations dataset.

dyskeratosis, hereditary benign intraepithelial Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, distal hereditary motor, type iia phenotype from the curated OMIM Gene-Disease Associations dataset.

{prostate cancer, hereditary, 5} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {prostate cancer, hereditary, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.

[hereditary persistence of alpha-fetoprotein] Gene Set

From 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 Set

From Reactome Pathways

proteins participating in the Defective AMN causes hereditary megaloblastic anemia 1 pathway from the Reactome Pathways dataset.

Defective CUBN causes hereditary megaloblastic anemia 1 Gene Set

From Reactome Pathways

proteins participating in the Defective CUBN causes hereditary megaloblastic anemia 1 pathway from the Reactome Pathways dataset.

Defective TCN2 causes hereditary megaloblastic anemia Gene Set

From Reactome Pathways

proteins participating in the Defective TCN2 causes hereditary megaloblastic anemia pathway from the Reactome Pathways dataset.