| Name |
|---|
Acquired Communicating Hydrocephalus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Communicating Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
communicating hydrocephalus Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease communicating hydrocephalus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
communicating hydrocephalus Gene SetFrom HPO Gene-Disease Associations genes associated with the communicating hydrocephalus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Communicating Hydrocephalus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Communicating Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Communicating hydrocephalus Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Communicating hydrocephalus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
absent posterior communicating artery Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent posterior communicating artery phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Megalencephaly polymicrogyria-polydactyly hydrocephalus syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Megalencephaly polymicrogyria-polydactyly hydrocephalus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hydrocephalus, nonsyndromic, autosomal recessive 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hydrocephalus, nonsyndromic, autosomal recessive 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked hydrocephalus syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked hydrocephalus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hydrocephalus Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hydrocephalus phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hydrocephalus, X-linked Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hydrocephalus, X-linked from the curated CTD Gene-Disease Associations dataset. |
Megalanecephaly Polymicrogyria-Polydactyly Hydrocephalus Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Megalanecephaly Polymicrogyria-Polydactyly Hydrocephalus Syndrome from the curated CTD Gene-Disease Associations dataset. |
Hydrocephalus Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hydrocephalus from the curated CTD Gene-Disease Associations dataset. |
obstructive hydrocephalus Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease obstructive hydrocephalus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
normal pressure hydrocephalus Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease normal pressure hydrocephalus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hydrocephalus Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hydrocephalus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hydrocephalus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hydrocephalus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hydrocephalus Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term hydrocephalus in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
hydrocephalus Gene SetFrom HPO Gene-Disease Associations genes associated with the hydrocephalus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
normal pressure hydrocephalus Gene SetFrom HPO Gene-Disease Associations genes associated with the normal pressure hydrocephalus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
severe hydrocephalus Gene SetFrom HPO Gene-Disease Associations genes associated with the severe hydrocephalus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Hydrocephalus, Normal Pressure Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hydrocephalus, Normal Pressure phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hydrocephalus Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hydrocephalus phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
hydrocephalus, nonsyndromic, autosomal recessive 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the hydrocephalus, nonsyndromic, autosomal recessive 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
bor-duane hydrocephalus contiguous gene syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the bor-duane hydrocephalus contiguous gene syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
hydrocephalus, nonsyndromic, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the hydrocephalus, nonsyndromic, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
hydrocephalus with hirschsprung disease Gene SetFrom OMIM Gene-Disease Associations genes associated with the hydrocephalus with hirschsprung disease phenotype from the curated OMIM Gene-Disease Associations dataset. |
hydrocephalus due to aqueductal stenosis Gene SetFrom OMIM Gene-Disease Associations genes associated with the hydrocephalus due to aqueductal stenosis phenotype from the curated OMIM Gene-Disease Associations dataset. |
hydrocephalus with congenital idiopathic intestinal pseudoobstruction Gene SetFrom OMIM Gene-Disease Associations genes associated with the hydrocephalus with congenital idiopathic intestinal pseudoobstruction phenotype from the curated OMIM Gene-Disease Associations dataset. |
Hydrocephalus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Idiopathic Normal Pressure Hydrocephalus (Inph) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Normal Pressure Hydrocephalus (Inph) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Hydrocephalus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Megalanecephaly Polymicrogyria-Polydactyly Hydrocephalus Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Megalanecephaly Polymicrogyria-Polydactyly Hydrocephalus Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
(Idiopathic) Normal Pressure Hydrocephalus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease (Idiopathic) Normal Pressure Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Obstructive Hydrocephalus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Obstructive Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hydrocephalus Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hydrocephalus Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Post-Traumatic Hydrocephalus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Post-Traumatic Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Arrested Hydrocephalus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Arrested Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
External Hydrocephalus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease External Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Post-Hemorrhagic Hydrocephalus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Post-Hemorrhagic Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Obstructive Hydrocephalus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Obstructive Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Vacterl Association With Hydrocephalus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Vacterl Association With Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Vacterl Association, X-Linked, With Or Without Hydrocephalus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Vacterl Association, X-Linked, With Or Without Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Vacterl Syndrome With Hydrocephalus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Vacterl Syndrome With Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Internal Hydrocephalus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Internal Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Megalencephaly, Polymicrogyria, Postaxial Polydactyly, Hydrocephalus Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Megalencephaly, Polymicrogyria, Postaxial Polydactyly, Hydrocephalus Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Vater Association With Hydrocephalus Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Vater Association With Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Severe Hydrocephalus Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hydrocephalus Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hydrocephalus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Normal pressure hydrocephalus Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Normal pressure hydrocephalus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Obstructive hydrocephalus Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Obstructive hydrocephalus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Severe hydrocephalus Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe hydrocephalus phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
X-linked hydrocephalus syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked hydrocephalus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hydrocephalus due to aqueductal stenosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hydrocephalus due to aqueductal stenosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hydrocephalus Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hydrocephalus phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital hydrocephalus Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital hydrocephalus phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Normal pressure hydrocephalus Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Normal pressure hydrocephalus phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Acquired long QT syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Acquired long QT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lipodystrophy, Partial, Acquired Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lipodystrophy, Partial, Acquired from the curated CTD Gene-Disease Associations dataset. |
Factor 8 deficiency, acquired Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Factor 8 deficiency, acquired from the curated CTD Gene-Disease Associations dataset. |
Acquired angioedema Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Acquired angioedema from the curated CTD Gene-Disease Associations dataset. |
Acquired Immunodeficiency Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Acquired Immunodeficiency Syndrome from the curated CTD Gene-Disease Associations dataset. |
Acquired Immunodeficiency Syndrome Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Acquired Immunodeficiency Syndrome in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
acquired metabolic disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease acquired metabolic disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
acquired metabolic disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease acquired metabolic disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
acquired immunodeficiency syndrome Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease acquired immunodeficiency syndrome in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
acquired thrombocytopenia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease acquired thrombocytopenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
acquired polycythemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease acquired polycythemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
acquired metabolic disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease acquired metabolic disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
acquired immunodeficiency syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease acquired immunodeficiency syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
acquired immunodeficiency syndrome; hiv infections; [x]human immunodeficiency virus disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
community-acquired infections; pneumonia, bacterial; pneumonia, viral Gene SetFrom GAD Gene-Disease Associations genes associated with the disease community-acquired infections; pneumonia, bacterial; pneumonia, viral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired immunodeficiency syndrome; cardiovascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; cardiovascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
community-acquired infections; pneumonia, bacterial; sepsis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease community-acquired infections; pneumonia, bacterial; sepsis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired immunodeficiency syndrome; chromosome deletion; hiv infections; [x]human immunodeficiency virus disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; chromosome deletion; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired immunodeficiency syndrome; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired immunodeficiency syndrome; aids dementia complex; aids related dementia complex; disease progression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; aids dementia complex; aids related dementia complex; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired immunodeficiency syndrome; hiv infections; pregnancy complications, infectious; [x]human immunodeficiency virus disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; hiv infections; pregnancy complications, infectious; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired immunodeficiency syndrome; aids-related opportunistic infections; cytomegalovirus retinitis; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; aids-related opportunistic infections; cytomegalovirus retinitis; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
community-acquired pneumonia (cap) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease community-acquired pneumonia (cap) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
articulation disorders; dyslexia, acquired; language disorders; noonan syndrome; turner's phenotype, karyotype normal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease articulation disorders; dyslexia, acquired; language disorders; noonan syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aplastic anemia, acquired Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aplastic anemia, acquired in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired immunodeficiency syndrome; hiv infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; hiv infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired immunodeficiency syndrome; disease progression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired immunodeficiency syndrome; substance abuse, intravenous Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; substance abuse, intravenous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
community-acquired infections; pneumonia; respiratory distress syndrome, adult Gene SetFrom GAD Gene-Disease Associations genes associated with the disease community-acquired infections; pneumonia; respiratory distress syndrome, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
community-acquired infections; pneumonia, bacterial; pneumonia, pneumococcal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease community-acquired infections; pneumonia, bacterial; pneumonia, pneumococcal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired immunodeficiency syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
community-acquired infections; pneumonia; septic shock; shock, septic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease community-acquired infections; pneumonia; septic shock; shock, septic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired immunodeficiency syndrome; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired immunodeficiency syndrome; hiv seropositivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; hiv seropositivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
community-acquired infections; pneumonia; sepsis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease community-acquired infections; pneumonia; sepsis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired immunodeficiency syndrome; kaposi sarcoma; lymphoma, aids-related; sarcoma, kaposi Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; kaposi sarcoma; lymphoma, aids-related; sarcoma, kaposi in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adult respiratory distress syndrome; community-acquired infections; pneumonia; respiratory distress syndrome, adult; septic shock; shock, septic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; community-acquired infections; pneumonia; respiratory distress syndrome, adult; septic shock; shock, septic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
community-acquired infections; pneumonia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease community-acquired infections; pneumonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired immunodeficiency syndrome; hiv infections; spondylarthropathies; [x]human immunodeficiency virus disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; hiv infections; spondylarthropathies; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acute-phase reaction; community-acquired infections; pneumonia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acute-phase reaction; community-acquired infections; pneumonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired immunodeficiency syndrome; aids-related opportunistic infections; cytomegalovirus retinitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; aids-related opportunistic infections; cytomegalovirus retinitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term acquired in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Simian Acquired Immune Deficiency Syndrome_T lymphocyte_GSE4785 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Simian Acquired Immune Deficiency Syndrome_T lymphocyte_GSE4785 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
Nephrotic syndrome (acquired) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Nephrotic syndrome (acquired) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
acquired metabolic disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease acquired metabolic disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
acquired immunodeficiency syndrome Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease acquired immunodeficiency syndrome in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
acquired abnormal hair pattern Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the acquired abnormal hair pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
acquired abnormal hair pattern Gene SetFrom HPO Gene-Disease Associations genes associated with the acquired abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Community-Acquired Infections Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Community-Acquired Infections phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Simian Acquired Immunodeficiency Syndrome Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Simian Acquired Immunodeficiency Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Dyslexia, Acquired Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Dyslexia, Acquired phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Acquired Hyperostosis Syndrome Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Acquired Hyperostosis Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Acquired Immunodeficiency Syndrome Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Acquired Immunodeficiency Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
{long qt syndrome 1, acquired, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {long qt syndrome 1, acquired, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{long qt syndrome 2, acquired, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {long qt syndrome 2, acquired, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{long qt syndrome, acquired, reduced susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {long qt syndrome, acquired, reduced susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{lipodystrophy, partial, acquired, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {lipodystrophy, partial, acquired, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
Community Acquired Pneumonia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Community Acquired Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Long Qt Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Long Qt Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Camptodactyly Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Camptodactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hospital Acquired Pneumonia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hospital Acquired Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dental Fluorosis, Acquired Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dental Fluorosis, Acquired in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Angioedema Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Angioedema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Aplastic Anemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Aplastic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Pectus Carinatum Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Pectus Carinatum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Kyphoscoliosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Kyphoscoliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Hypogammaglobulinemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Hypogammaglobulinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Hallux Valgus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Hallux Valgus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Acquired Sideroblastic Anemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Acquired Sideroblastic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thrombotic Thrombocytopenic Purpura, Acquired Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thrombotic Thrombocytopenic Purpura, Acquired in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Porencephaly Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Porencephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chronic Acquired Lymphedema Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chronic Acquired Lymphedema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Partial Lipodystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Partial Lipodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Hypoparathyroidism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Hypoparathyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Flat Foot Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Flat Foot in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Metabolic Disorder, Central Nervous System, Acquired Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Metabolic Disorder, Central Nervous System, Acquired in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Thrombocytopenia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Thrombocytopenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Nephrogenic Diabetes Insipidus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Nephrogenic Diabetes Insipidus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Phimosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Phimosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Hypofibrinogenemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Hypofibrinogenemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Von Willebrand'S Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Von Willebrand'S Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Cubitus Valgus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Cubitus Valgus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Acquired Melanosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Acquired Melanosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Hypothyroidism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Hypothyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypocalciuric Hypercalcemia, Acquired Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypocalciuric Hypercalcemia, Acquired in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Thrombophilia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Thrombophilia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Atrophy Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Atrophy Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Obstructive Azoospermia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Obstructive Azoospermia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adult Acquired Toxoplasmosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adult Acquired Toxoplasmosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Neuromyotonia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Neuromyotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Haemophilia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Haemophilia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Factor 8 Deficiency, Acquired Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Factor 8 Deficiency, Acquired in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Immunodeficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Immunodeficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Clubfoot Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Clubfoot in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Cystic Kidney Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Cystic Kidney Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Polyneuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Polyneuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Protein S Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Protein S Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Anomaly Of Tongue Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Anomaly Of Tongue in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Hypophosphatemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Hypophosphatemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Methemoglobinemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Methemoglobinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Deformity Of Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Deformity Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Platelet Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Platelet Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Sensorineural Hearing Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Sensorineural Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hospital Acquired Bacterial Pneumonia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hospital Acquired Bacterial Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Cystic Disease Associated Renal Cell Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Cystic Disease Associated Renal Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Renal Cystic Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Renal Cystic Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Immunodeficiency Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Immunodeficiency Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Factor Xiii Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Factor Xiii Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Generalized Lipodystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Generalized Lipodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Hypogonadotropic Hypogonadism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Hypogonadotropic Hypogonadism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Trigger Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Trigger Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Acquired Nasolacrimal Duct Obstruction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Acquired Nasolacrimal Duct Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Torsion Dystonia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Torsion Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Cjd Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Cjd in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Prion Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Prion Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Protein C Deficiency, Acquired Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Protein C Deficiency, Acquired in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Fanconi Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Fanconi Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Antithrombin Iii Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Antithrombin Iii Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired C1 Inhibitor Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired C1 Inhibitor Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Factor X Deficiency Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Factor X Deficiency Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Immunodeficiency Syndrome Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acquired Immunodeficiency Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Acquired Meningomyelocele Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acquired Meningomyelocele in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Acquired Genu Recurvatum Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acquired Genu Recurvatum in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Acquired Amegakaryocytic Thrombocytopenia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acquired Amegakaryocytic Thrombocytopenia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Acquired Hearing Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acquired Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Acquired Purpura Fulminans Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acquired Purpura Fulminans in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Acquired partial lipodystrophy Barraquer Simons syndrome Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Acquired partial lipodystrophy Barraquer Simons syndrome pathway from the WikiPathways Pathways 2024 dataset. |
Acquired metabolic disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Acquired metabolic disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Acquired metabolic disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Acquired metabolic disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired immunodeficiency syndrome Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Acquired immunodeficiency syndrome in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired metabolic disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired metabolic disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired immunodeficiency syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired immunodeficiency syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired thrombocytopenia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired thrombocytopenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired generalized lipodystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired generalized lipodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired angioedema Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired angioedema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired hyperkeratosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired hyperkeratosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired hemangioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired hemangioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired night blindness Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired night blindness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired von Willebrand syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired von Willebrand syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired polycythemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired polycythemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired gastric outlet stenosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired gastric outlet stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired laryngomalacia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired laryngomalacia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired tear duct stenosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired tear duct stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired color blindness Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired color blindness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Leukodystrophy and acquired microcephaly Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Leukodystrophy and acquired microcephaly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Acquired hemoglobin H disease Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Acquired hemoglobin H disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Acquired partial lipodystrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Acquired partial lipodystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Acquired polycythemia vera Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Acquired polycythemia vera phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Genetic non-acquired premature ovarian failure Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Genetic non-acquired premature ovarian failure phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Non-acquired combined pituitary hormone deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Non-acquired combined pituitary hormone deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Nephrotic syndrome (acquired) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Nephrotic syndrome (acquired) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |