Riboflavin and CoQ disorders

Clear Filter

Results for "Riboflavin and CoQ disorders": 1001 gene sets

Name
Riboflavin and CoQ disorders Gene Set From WikiPathways Pathways 2024 proteins participating in the Riboflavin and CoQ disorders pathway from the WikiPathways Pathways 2024 dataset.
cocaine-related disorders; opioid-related disorders; substance-related disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease cocaine-related disorders; opioid-related disorders; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fatigue; sleep disorders; sleep initiation and maintenance disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease fatigue; sleep disorders; sleep initiation and maintenance disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcohol-related disorders; cocaine-related disorders; Gene Set From GAD Gene-Disease Associations genes associated with the disease alcohol-related disorders; cocaine-related disorders; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
speech disorders; substance-related disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease speech disorders; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholism; opioid-related disorders; substance-related disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholism; opioid-related disorders; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholism; cocaine-related disorders; heroin dependence; substance-related disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholism; cocaine-related disorders; heroin dependence; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders; puerperal disorders; sinus thrombosis, intracranial Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; puerperal disorders; sinus thrombosis, intracranial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hearing loss, sensorineural; learning disorders; melas syndrome; migraine disorders; mitochondrial diseases; sensorineural hearing loss Gene Set From GAD Gene-Disease Associations genes associated with the disease hearing loss, sensorineural; learning disorders; melas syndrome; migraine disorders; mitochondrial diseases; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
craniofacial abnormalities; growth disorders; learning disorders; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease craniofacial abnormalities; growth disorders; learning disorders; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
articulation disorders; disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease articulation disorders; disorders 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 Set From 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.
alzheimer disease; alzheimer's disease; disorders of excessive somnolence; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; disorders of excessive somnolence; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders; blood coagulation disorders, inherited; recurrence; thromboembolism; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; blood coagulation disorders, inherited; recurrence; thromboembolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
personality disorders; eating disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease personality disorders; eating disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
learning disorders; memory disorders; mental retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease learning disorders; memory disorders; mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
migraine disorders; substance-related disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease migraine disorders; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; growth disorders; nutrition disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; growth disorders; nutrition disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain injuries; cerebrovascular disorders; migraine disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease brain injuries; cerebrovascular disorders; migraine disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apnea; apoplexy; blood coagulation disorders; brain ischemia; cerebrovascular disorders; hypotony, muscle; muscle hypotonia; protein c deficiency; seizures; stroke; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease apnea; apoplexy; blood coagulation disorders; brain ischemia; cerebrovascular disorders; hypotony, muscle; muscle hypotonia; protein c deficiency; seizures; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
riboflavin-6822 Gene Set From CMAP Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the riboflavin-6822 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.
riboflavin-2760 Gene Set From CMAP Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the riboflavin-2760 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.
riboflavin-1767 Gene Set From CMAP Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the riboflavin-1767 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.
riboflavin-4485 Gene Set From CMAP Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the riboflavin-4485 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.
Riboflavin Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Riboflavin from the curated CTD Gene-Chemical Interactions dataset.
Riboflavin Monophosphate Gene Set From DrugBank Drug Targets interacting proteins for the Riboflavin Monophosphate drug from the curated DrugBank Drug Targets dataset.
Riboflavin Gene Set From DrugBank Drug Targets interacting proteins for the Riboflavin drug from the curated DrugBank Drug Targets dataset.
folic acid deficiency; fractures, bone; osteoporosis, postmenopausal; riboflavin deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease folic acid deficiency; fractures, bone; osteoporosis, postmenopausal; riboflavin deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
riboflavin Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term riboflavin in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
riboflavin transport Gene Set From GO Biological Process Annotations 2015 genes participating in the riboflavin transport biological process from the curated GO Biological Process Annotations 2015 dataset.
riboflavin metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the riboflavin metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
riboflavin biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the riboflavin biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
riboflavin reductase (nadph) activity Gene Set From GO Molecular Function Annotations 2015 genes performing the riboflavin reductase (nadph) activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
riboflavin kinase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the riboflavin kinase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
riboflavin transporter activity Gene Set From GO Molecular Function Annotations 2015 genes performing the riboflavin transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
Riboflavin Gene Set From HMDB Metabolites of Enzymes interacting proteins for the Riboflavin metabolite from the curated HMDB Metabolites of Enzymes dataset.
Riboflavin reduced Gene Set From HMDB Metabolites of Enzymes interacting proteins for the Riboflavin reduced metabolite from the curated HMDB Metabolites of Enzymes dataset.
Riboflavin synthase-like beta-barrel Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Riboflavin synthase-like beta-barrel protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Riboflavin kinase domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Riboflavin kinase domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Riboflavin kinase Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Riboflavin kinase protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Riboflavin kinase domain, bacterial/eukaryotic Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Riboflavin kinase domain, bacterial/eukaryotic protein domain from the InterPro Predicted Protein Domain Annotations dataset.
riboflavin metabolism Gene Set From KEGG Pathways proteins participating in the riboflavin metabolism pathway from the KEGG Pathways dataset.
riboflavin deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the riboflavin deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
Vitamin B2 (riboflavin) metabolism Gene Set From Reactome Pathways 2014 proteins participating in the Vitamin B2 (riboflavin) metabolism pathway from the Reactome Pathways dataset.
Riboflavin Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Riboflavin Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
riboflavin metabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the riboflavin metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
riboflavin biosynthetic process Gene Set From GO Biological Process Annotations 2023 genes participating in the riboflavin biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset.
riboflavin transport Gene Set From GO Biological Process Annotations 2023 genes participating in the riboflavin transport biological process from the curated GO Biological Process Annotations 2023 dataset.
riboflavin reductase (NADPH) activity Gene Set From GO Molecular Function Annotations 2023 genes performing the riboflavin reductase (NADPH) activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
riboflavin kinase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the riboflavin kinase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
riboflavin transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2023 genes performing the riboflavin transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
Riboflavin Gene Set From MW Enzyme Metabolite Associations interacting proteins for Riboflavin metabolite from the MW Gene Metabolite Associations dataset.
Vitamin B2 (riboflavin) metabolism Gene Set From Reactome Pathways 2024 proteins participating in the Vitamin B2 (riboflavin) metabolism pathway from the Reactome Pathways 2024 dataset.
riboflavin metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the riboflavin metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
riboflavin biosynthetic process Gene Set From GO Biological Process Annotations 2025 genes participating in the riboflavin biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.
riboflavin transport Gene Set From GO Biological Process Annotations 2025 genes participating in the riboflavin transport biological process from the curated GO Biological Process Annotations 2025 dataset.
riboflavin reductase (NADPH) activity Gene Set From GO Molecular Function Annotations 2025 genes performing the riboflavin reductase (NADPH) activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
riboflavin kinase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the riboflavin kinase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
riboflavin transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2025 genes performing the riboflavin transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
riboflavin binding Gene Set From GO Molecular Function Annotations 2025 genes performing the riboflavin binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Riboflavin deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Riboflavin deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Riboflavin synthase complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Riboflavin synthase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Maternal riboflavin deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Maternal riboflavin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Riboflavin metabolism Gene Set From KEGG Pathways 2026 proteins participating in the Riboflavin metabolism pathway from the KEGG Pathways 2026 dataset.
RIBOFLAVIN Gene Set From DGIdb Drug Targets 2026 interacting proteins for the RIBOFLAVIN drug from theDGIdb Drug Targets 2026 dataset.
Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Set From Reactome Pathways 2014 proteins participating in the Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways dataset.
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Epilepsy, X-linked, with variable learning disabilities and behavior disorders Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, X-linked, with variable learning disabilities and behavior disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Schizophrenia and Disorders with Psychotic Features Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Schizophrenia and Disorders with Psychotic Features from the curated CTD Gene-Disease Associations dataset.
Sleep Initiation and Maintenance Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sleep Initiation and Maintenance Disorders from the curated CTD Gene-Disease Associations dataset.
Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders from the curated CTD Gene-Disease Associations dataset.
Attention Deficit and Disruptive Behavior Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Attention Deficit and Disruptive Behavior Disorders from the curated CTD Gene-Disease Associations dataset.
Attention Deficit and Disruptive Behavior Disorders Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Attention Deficit and Disruptive Behavior Disorders in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
attention deficit and disruptive behavior disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease attention deficit and disruptive behavior disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcohol-related disorders; carcinoma, squamous cell; head and neck neoplasms; squamous cell carcinoma; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease alcohol-related disorders; carcinoma, squamous cell; head and neck neoplasms; squamous cell carcinoma; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fatigue; sleep initiation and maintenance disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease fatigue; sleep initiation and maintenance disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep initiation and maintenance disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep initiation and maintenance disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin; obesity; blood pressure, arterial; blood and blood forming organ disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin; obesity; blood pressure, arterial; blood and blood forming organ disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood and blood forming organ disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease blood and blood forming organ disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neuroticism, major depression, and anxiety disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease neuroticism, major depression, and anxiety disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenocarcinoma; carcinoma, squamous cell; deglutition disorders; head and neck neoplasms; radiodermatitis Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, squamous cell; deglutition disorders; head and neck neoplasms; radiodermatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
elevated blood pressure and personality disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease elevated blood pressure and personality disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
puberty and gonadal disorders Gene Set From GWASdb SNP-Phenotype Associations genes associated with the puberty and gonadal disorders phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
puberty and gonadal disorders Gene Set From HPO Gene-Disease Associations genes associated with the puberty and gonadal disorders phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Sleep Initiation and Maintenance Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep Initiation and Maintenance Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Attention Deficit and Disruptive Behavior Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Attention Deficit and Disruptive Behavior Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
epilepsy, x-linked, with variable learning disabilities and behavior disorders Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, x-linked, with variable learning disabilities and behavior disorders phenotype from the curated OMIM Gene-Disease Associations dataset.
Trauma And Stressor Related Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Trauma And Stressor Related Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sleep Initiation And Maintenance Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sleep Initiation And Maintenance Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Prostatic Disorders (Excl Infections And Inflammations) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Prostatic Disorders (Excl Infections And Inflammations) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reaction To Severe Stress, And Adjustment Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reaction To Severe Stress, And Adjustment Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Other Specified Extrapyramidal And Movement Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Other Specified Extrapyramidal And Movement Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Disorders Of Both Mitral And Tricuspid Valves Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Disorders Of Both Mitral And Tricuspid Valves in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
General Disorders And Administration Site Conditions Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease General Disorders And Administration Site Conditions in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Purine metabolism and related disorders Gene Set From WikiPathways Pathways 2024 proteins participating in the Purine metabolism and related disorders pathway from the WikiPathways Pathways 2024 dataset.
Vitamin B6 dependent and responsive disorders Gene Set From WikiPathways Pathways 2024 proteins participating in the Vitamin B6 dependent and responsive disorders pathway from the WikiPathways Pathways 2024 dataset.
Disorders of folate metabolism and transport Gene Set From WikiPathways Pathways 2024 proteins participating in the Disorders of folate metabolism and transport pathway from the WikiPathways Pathways 2024 dataset.
Methionine metabolism leading to sulfur amino acids and related disorders Gene Set From WikiPathways Pathways 2024 proteins participating in the Methionine metabolism leading to sulfur amino acids and related disorders pathway from the WikiPathways Pathways 2024 dataset.
Tyrosine metabolism and related disorders Gene Set From WikiPathways Pathways 2024 proteins participating in the Tyrosine metabolism and related disorders pathway from the WikiPathways Pathways 2024 dataset.
FGF23 signaling in hypophosphatemic rickets and related disorders Gene Set From WikiPathways Pathways 2024 proteins participating in the FGF23 signaling in hypophosphatemic rickets and related disorders pathway from the WikiPathways Pathways 2024 dataset.
Disorders of bile acid synthesis and biliary transport Gene Set From WikiPathways Pathways 2024 proteins participating in the Disorders of bile acid synthesis and biliary transport pathway from the WikiPathways Pathways 2024 dataset.
X-linked epilepsy with variable learning disabilities and behavior disorders Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked epilepsy with variable learning disabilities and behavior disorders in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Joubert syndrome and related disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Joubert syndrome and related disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
CACNA1D-related neurodevelopmental and endocrine disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the CACNA1D-related neurodevelopmental and endocrine disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Response to cognitive-behavioural therapy in anxiety and major depressive disorders Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to cognitive-behavioural therapy in anxiety and major depressive disorders phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Anxiety and stress-related disorders Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Anxiety and stress-related disorders phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Anxiety and stress-related disorders (excluding adjustment disorder) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Anxiety and stress-related disorders (excluding adjustment disorder) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Anxiety and stress-related disorders (excluding co-morbid schizophrenia) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Anxiety and stress-related disorders (excluding co-morbid schizophrenia) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Anxiety and stress-related disorders (including obsessive-compulsive disorder) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Anxiety and stress-related disorders (including obsessive-compulsive disorder) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Anxiety and stress-related disorders (psychiatric co-morbidity weighting design) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Anxiety and stress-related disorders (psychiatric co-morbidity weighting design) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Anxiety and stress-related disorders (psychiatric co-morbidity covariate model) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Anxiety and stress-related disorders (psychiatric co-morbidity covariate model) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression Gene Set From Biocarta Pathways proteins participating in the basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression pathway from the Biocarta Pathways 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.
Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Coloboma, uveal, with cleft lip and palate and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Coloboma, uveal, with cleft lip and palate and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diabetes mellitus AND insipidus with optic atrophy AND deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset.
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation 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.
Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia 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.
Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations from the curated CTD Gene-Disease Associations dataset.
postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations Gene Set From GAD Gene-Disease Associations genes associated with the disease postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anxiety and hostility and depression Gene Set From GAD Gene-Disease Associations genes associated with the disease anxiety and hostility and depression 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.
frontotemporal dementia and pick-like 3r and 4r tauopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease frontotemporal dementia and pick-like 3r and 4r tauopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations Gene Set From GAD Gene-Disease Associations genes associated with the disease adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
squamous cell carcinomas of the head and neck (scchn) and breast cancer Gene Set From GAD Gene-Disease Associations genes associated with the disease squamous cell carcinomas of the head and neck (scchn) and breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vitamins and metabolites in pregnant women and neonates Gene Set From GAD Gene-Disease Associations genes associated with the disease vitamins and metabolites in pregnant women and neonates in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
racemase and epimerase activity, acting on amino acids and derivatives Gene Set From GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on amino acids and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset.
racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set From GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset.
leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation Gene Set From OMIM Gene-Disease Associations genes associated with the leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation phenotype from the curated OMIM Gene-Disease Associations dataset.
microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma Gene Set From OMIM Gene-Disease Associations genes associated with the microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset.
hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set From OMIM Gene-Disease Associations genes associated with the hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies Gene Set From OMIM Gene-Disease Associations genes associated with the craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Set From Reactome Pathways 2014 proteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways dataset.
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Set From Reactome Pathways 2014 proteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways dataset.
PI and PC transport between ER and Golgi membranes Gene Set From Reactome Pathways 2014 proteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways dataset.
Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Set From Reactome Pathways 2014 proteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways dataset.
FGFR1c and Klotho ligand binding and activation Gene Set From Reactome Pathways 2014 proteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways dataset.
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Set From Reactome Pathways 2014 proteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways dataset.
Synthesis and processing of ENV and VPU Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways dataset.
Synthesis and interconversion of nucleotide di- and triphosphates Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis and interconversion of nucleotide di- and triphosphates pathway from the Reactome Pathways dataset.
SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anal Intraepithelial Neoplasia I And Ii (Ain I And Ii) (Histologically Confirmed) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anal Intraepithelial Neoplasia I And Ii (Ain I And Ii) (Histologically Confirmed) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pierre Robin Sequence With Pectus Excavatum And Rib And Scapular Anomalies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pierre Robin Sequence With Pectus Excavatum And Rib And Scapular Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set From GO Molecular Function Annotations 2023 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2023 dataset.
SRF and miRs in smooth muscle differentiation and proliferation Gene Set From WikiPathways Pathways 2024 proteins participating in the SRF and miRs in smooth muscle differentiation and proliferation pathway from the WikiPathways Pathways 2024 dataset.
SREBF and miR33 in cholesterol and lipid homeostasis Gene Set From WikiPathways Pathways 2024 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis pathway from the WikiPathways Pathways 2024 dataset.
RIOK1 and RIOK2 in EGFR and PI3K mediated tumorigenesis Gene Set From WikiPathways Pathways 2024 proteins participating in the RIOK1 and RIOK2 in EGFR and PI3K mediated tumorigenesis pathway from the WikiPathways Pathways 2024 dataset.
ApoE and miR 146 in inflammation and atherosclerosis Gene Set From WikiPathways Pathways 2024 proteins participating in the ApoE and miR 146 in inflammation and atherosclerosis pathway from the WikiPathways Pathways 2024 dataset.
Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine Gene Set From WikiPathways Pathways 2024 proteins participating in the Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine pathway from the WikiPathways Pathways 2024 dataset.
Somatroph axis GH and its relationship to dietary restriction and aging Gene Set From WikiPathways Pathways 2024 proteins participating in the Somatroph axis GH and its relationship to dietary restriction and aging pathway from the WikiPathways Pathways 2024 dataset.
Mechanoregulation and pathology of YAP TAZ via Hippo and non Hippo mechanisms Gene Set From WikiPathways Pathways 2024 proteins participating in the Mechanoregulation and pathology of YAP TAZ via Hippo and non Hippo mechanisms pathway from the WikiPathways Pathways 2024 dataset.
GLP 1 from intestine and pancreas and role in glucose homeostasis Gene Set From WikiPathways Pathways 2024 proteins participating in the GLP 1 from intestine and pancreas and role in glucose homeostasis pathway from the WikiPathways Pathways 2024 dataset.
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Set From Reactome Pathways 2024 proteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways 2024 dataset.
Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) Gene Set From Reactome Pathways 2024 proteins participating in the Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) pathway from the Reactome Pathways 2024 dataset.
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Set From Reactome Pathways 2024 proteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways 2024 dataset.
FGFR1c and Klotho ligand binding and activation Gene Set From Reactome Pathways 2024 proteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways 2024 dataset.
MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis Gene Set From Reactome Pathways 2024 proteins participating in the MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis pathway from the Reactome Pathways 2024 dataset.
Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Set From Reactome Pathways 2024 proteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways 2024 dataset.
PI and PC transport between ER and Golgi membranes Gene Set From Reactome Pathways 2024 proteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways 2024 dataset.
PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 Gene Set From Reactome Pathways 2024 proteins participating in the PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 pathway from the Reactome Pathways 2024 dataset.
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks Gene Set From Reactome Pathways 2024 proteins participating in the Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks pathway from the Reactome Pathways 2024 dataset.
Synthesis and processing of ENV and VPU Gene Set From Reactome Pathways 2024 proteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways 2024 dataset.
Transcriptional and post-translational regulation of MITF-M expression and activity Gene Set From Reactome Pathways 2024 proteins participating in the Transcriptional and post-translational regulation of MITF-M expression and activity pathway from the Reactome Pathways 2024 dataset.
Transport of bile salts and organic acids, metal ions and amine compounds Gene Set From Reactome Pathways 2024 proteins participating in the Transport of bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways 2024 dataset.
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Set From Reactome Pathways 2024 proteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways 2024 dataset.
racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set From GO Molecular Function Annotations 2025 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vertebral anomalies and variable endocrine and T-cell dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Vertebral anomalies and variable endocrine and T-cell dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Regulation of gene expression and signal transduction in immune and stress responses Gene Set From CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of gene expression and signal transduction in immune and stress responses assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.
Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
FLNB-Related Disorders Gene Set From ClinVar Gene-Phenotype Associations genes associated with the FLNB-Related Disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NSDHL-Related Disorders Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NSDHL-Related Disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
WFS1-Related Disorders Gene Set From ClinVar Gene-Phenotype Associations genes associated with the WFS1-Related Disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MYH9 related disorders Gene Set From ClinVar Gene-Phenotype Associations genes associated with the MYH9 related disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Child Development Disorders, Pervasive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Child Development Disorders, Pervasive from the curated CTD Gene-Disease Associations dataset.
Opioid-Related Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Opioid-Related Disorders from the curated CTD Gene-Disease 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.
Language Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Language Disorders from the curated CTD Gene-Disease Associations dataset.
Child Behavior Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Child Behavior Disorders from the curated CTD Gene-Disease Associations dataset.
Movement Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Movement Disorders from the curated CTD Gene-Disease Associations dataset.
Chronobiology Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Chronobiology Disorders from the curated CTD Gene-Disease Associations dataset.
Consciousness Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Consciousness Disorders from the curated CTD Gene-Disease Associations dataset.
Olfaction Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Olfaction Disorders from the curated CTD Gene-Disease Associations dataset.
Mood Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mood Disorders from the curated CTD Gene-Disease Associations dataset.
Alcohol-Related Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alcohol-Related Disorders from the curated CTD Gene-Disease Associations dataset.
Alcohol-Induced Disorders, Nervous System Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alcohol-Induced Disorders, Nervous System from the curated CTD Gene-Disease Associations dataset.
Cognition Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cognition Disorders from the curated CTD Gene-Disease Associations dataset.
Iron Metabolism Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Iron Metabolism Disorders from the curated CTD Gene-Disease Associations dataset.
DNA Repair-Deficiency Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease DNA Repair-Deficiency Disorders from the curated CTD Gene-Disease Associations dataset.
Anxiety Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anxiety Disorders from the curated CTD Gene-Disease Associations dataset.
Phobic Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Phobic Disorders from the curated CTD Gene-Disease Associations dataset.
Fetal Alcohol Spectrum Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fetal Alcohol Spectrum Disorders from the curated CTD Gene-Disease Associations dataset.
Somatoform Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Somatoform Disorders from the curated CTD Gene-Disease Associations dataset.
46, XY Disorders of Sex Development Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease 46, XY Disorders of Sex Development from the curated CTD Gene-Disease Associations dataset.
Mental Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Disorders from the curated CTD Gene-Disease Associations dataset.
Affective Disorders, Psychotic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Affective Disorders, Psychotic from the curated CTD Gene-Disease Associations dataset.
Paranoid Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Paranoid Disorders from the curated CTD Gene-Disease Associations dataset.
Learning Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Learning Disorders from the curated CTD Gene-Disease Associations dataset.
Histiocytic Disorders, Malignant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Histiocytic Disorders, Malignant from the curated CTD Gene-Disease Associations dataset.
Growth Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Growth Disorders from the curated CTD Gene-Disease Associations dataset.
Stress Disorders, Post-Traumatic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Stress Disorders, Post-Traumatic from the curated CTD Gene-Disease Associations dataset.
Vision Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vision Disorders from the curated CTD Gene-Disease Associations dataset.
Respiration Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Respiration Disorders from the curated CTD Gene-Disease Associations dataset.
Taste Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Taste Disorders from the curated CTD Gene-Disease Associations dataset.
Hearing Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hearing Disorders from the curated CTD Gene-Disease Associations dataset.
Photosensitivity Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Photosensitivity Disorders from the curated CTD Gene-Disease Associations dataset.
Cocaine-Related Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cocaine-Related Disorders from the curated CTD Gene-Disease Associations dataset.
Peroxisome biogenesis disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Peroxisome biogenesis disorders from the curated CTD Gene-Disease Associations dataset.
Myeloproliferative Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myeloproliferative Disorders from the curated CTD Gene-Disease Associations dataset.
Disorders of Excessive Somnolence Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Disorders of Excessive Somnolence from the curated CTD Gene-Disease Associations dataset.
Temporomandibular Joint Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Temporomandibular Joint Disorders from the curated CTD Gene-Disease Associations dataset.
Substance-Related Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Substance-Related Disorders from the curated CTD Gene-Disease Associations dataset.
Somatosensory Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Somatosensory Disorders from the curated CTD Gene-Disease Associations dataset.
Ciliary Motility Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ciliary Motility Disorders from the curated CTD Gene-Disease Associations dataset.
Psychophysiologic Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Psychophysiologic Disorders from the curated CTD Gene-Disease Associations dataset.
Deglutition Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deglutition Disorders from the curated CTD Gene-Disease Associations dataset.
Disorders of Environmental Origin Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Disorders of Environmental Origin from the curated CTD Gene-Disease Associations dataset.
Speech Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Speech Disorders from the curated CTD Gene-Disease Associations dataset.
Immunoproliferative Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Immunoproliferative Disorders from the curated CTD Gene-Disease Associations dataset.
Auditory Perceptual Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Auditory Perceptual Disorders from the curated CTD Gene-Disease Associations dataset.
Lipid Metabolism Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lipid Metabolism Disorders from the curated CTD Gene-Disease Associations dataset.
Leukocyte Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leukocyte Disorders from the curated CTD Gene-Disease Associations dataset.
Pupil Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pupil Disorders from the curated CTD Gene-Disease Associations dataset.
Mental Disorders Diagnosed in Childhood Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Disorders Diagnosed in Childhood from the curated CTD Gene-Disease Associations dataset.
Memory Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Memory Disorders from the curated CTD Gene-Disease Associations dataset.
Blood Coagulation Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Blood Coagulation Disorders from the curated CTD Gene-Disease Associations dataset.
Gonadal Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gonadal Disorders from the curated CTD Gene-Disease Associations dataset.
Language Development Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Language Development Disorders from the curated CTD Gene-Disease Associations dataset.
Blood Platelet Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Blood Platelet Disorders from the curated CTD Gene-Disease Associations dataset.
Chromosome Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Chromosome Disorders from the curated CTD Gene-Disease Associations dataset.
Glucose Metabolism Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glucose Metabolism Disorders from the curated CTD Gene-Disease Associations dataset.
Ocular Motility Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ocular Motility Disorders from the curated CTD Gene-Disease Associations dataset.
Delirium, Dementia, Amnestic, Cognitive Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Delirium, Dementia, Amnestic, Cognitive Disorders from the curated CTD Gene-Disease Associations dataset.
Impulse Control Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Impulse Control Disorders from the curated CTD Gene-Disease Associations dataset.
Migraine Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Migraine Disorders from the curated CTD Gene-Disease Associations dataset.
Peroxisomal Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Peroxisomal Disorders from the curated CTD Gene-Disease Associations dataset.
Pigmentation Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pigmentation Disorders from the curated CTD Gene-Disease Associations dataset.
Lymphoproliferative Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lymphoproliferative Disorders from the curated CTD Gene-Disease Associations dataset.
Sleep Disorders, Circadian Rhythm Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sleep Disorders, Circadian Rhythm from the curated CTD Gene-Disease Associations dataset.
Dissociative Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dissociative Disorders from the curated CTD Gene-Disease Associations dataset.
Puerperal Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Puerperal Disorders from the curated CTD Gene-Disease Associations dataset.
Eating Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Eating Disorders from the curated CTD Gene-Disease Associations dataset.
Urination Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Urination Disorders from the curated CTD Gene-Disease Associations dataset.
Personality Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Personality Disorders from the curated CTD Gene-Disease Associations dataset.
MYH9-Related Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYH9-Related Disorders from the curated CTD Gene-Disease Associations dataset.
Psychomotor Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Psychomotor Disorders from the curated CTD Gene-Disease Associations dataset.
46, XX Disorders of Sex Development Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease 46, XX Disorders of Sex Development from the curated CTD Gene-Disease Associations dataset.
Amphetamine-Related Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Amphetamine-Related Disorders from the curated CTD Gene-Disease Associations dataset.
Gait Disorders, Neurologic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gait Disorders, Neurologic from the curated CTD Gene-Disease Associations dataset.
Heat Stress Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Heat Stress Disorders from the curated CTD Gene-Disease Associations dataset.
Motor Skills Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Motor Skills Disorders from the curated CTD Gene-Disease Associations dataset.
Sensation Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sensation Disorders from the curated CTD Gene-Disease Associations dataset.
Perceptual Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Perceptual Disorders from the curated CTD Gene-Disease Associations dataset.
Psychotic Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Psychotic Disorders from the curated CTD Gene-Disease Associations dataset.
Heredodegenerative Disorders, Nervous System Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Heredodegenerative Disorders, Nervous System from the curated CTD Gene-Disease Associations dataset.
Adjustment Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Adjustment Disorders from the curated CTD Gene-Disease Associations dataset.
Tic Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Tic Disorders from the curated CTD Gene-Disease Associations dataset.
Dystonic Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dystonic Disorders from the curated CTD Gene-Disease Associations dataset.
Blood Coagulation Disorders, Inherited Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Blood Coagulation Disorders, Inherited from the curated CTD Gene-Disease Associations dataset.
Cerebrovascular Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebrovascular Disorders from the curated CTD Gene-Disease Associations dataset.
Phosphorus Metabolism Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Phosphorus Metabolism Disorders from the curated CTD Gene-Disease Associations dataset.
Sleep Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sleep Disorders from the curated CTD Gene-Disease Associations dataset.
Parkinsonian Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Parkinsonian Disorders from the curated CTD Gene-Disease Associations dataset.
Disorders of Sex Development Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Disorders of Sex Development from the curated CTD Gene-Disease Associations dataset.
Fetal Nutrition Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fetal Nutrition Disorders from the curated CTD Gene-Disease Associations dataset.
Mental Disorders Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Mental Disorders in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Myeloproliferative Disorders Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Myeloproliferative Disorders in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Neurotic Disorders Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Neurotic Disorders in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Respiration Disorders Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Respiration Disorders in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Movement Disorders Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Movement Disorders in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Mood Disorders Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Mood Disorders in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Substance-Related Disorders Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Substance-Related Disorders in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Migraine Disorders Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Migraine Disorders in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
hemorrhage; myeloproliferative disorders; thrombosis; vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease hemorrhage; myeloproliferative disorders; thrombosis; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
menstrual disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease menstrual disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood platelet disorders; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease blood platelet disorders; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
migraine disorders; tension-type headache Gene Set From GAD Gene-Disease Associations genes associated with the disease migraine disorders; tension-type headache in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
manic depressive disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease manic depressive disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pregnancy complications, hematologic; puerperal disorders; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease pregnancy complications, hematologic; puerperal disorders; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral infarction; memory disorders; subarachnoid hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral infarction; memory disorders; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; puerperal disorders; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; puerperal disorders; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; growth disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; growth disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
burkitt lymphoma; hodgkin disease; lymphoma, non-hodgkin; lymphoma, non-hodgkin's; lymphoproliferative disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease burkitt lymphoma; hodgkin disease; lymphoma, non-hodgkin; lymphoma, non-hodgkin's; lymphoproliferative disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lymphoma; myeloproliferative disorders; polycythemia vera; thrombocythemia, essential Gene Set From GAD Gene-Disease Associations genes associated with the disease lymphoma; myeloproliferative disorders; polycythemia vera; thrombocythemia, essential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcohol-related disorders; neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease alcohol-related disorders; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lipid metabolism disorders; metabolic syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease lipid metabolism disorders; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apnea; opioid-related disorders; pain Gene Set From GAD Gene-Disease Associations genes associated with the disease apnea; opioid-related disorders; pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bedwetting; constipation; diurnal enuresis; nocturnal enuresis; sleep arousal disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease bedwetting; constipation; diurnal enuresis; nocturnal enuresis; sleep arousal disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperprolactinemia; tic disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperprolactinemia; tic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyotrophic lateral sclerosis; iron metabolism disorders; nerve degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease amyotrophic lateral sclerosis; iron metabolism disorders; nerve degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
disorders; premenstrual syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease disorders; premenstrual syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyotrophic lateral sclerosis; chromosome disorders; Gene Set From GAD Gene-Disease Associations genes associated with the disease amyotrophic lateral sclerosis; chromosome disorders; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myeloproliferative disorders; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease myeloproliferative disorders; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebrovascular disorders; dementia Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebrovascular disorders; dementia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; cerebrovascular disorders; Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; cerebrovascular disorders; 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.
birth weight; growth disorders; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; growth disorders; insulin resistance 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.
migraine disorders; migraine with aura Gene Set From GAD Gene-Disease Associations genes associated with the disease migraine disorders; migraine with aura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral hemorrhage; cerebral hemorrhages; cerebrovascular disorders; hypertension Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral hemorrhage; cerebral hemorrhages; cerebrovascular disorders; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders; cardiovascular diseases; optic neuropathy, ischemic Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; cardiovascular diseases; optic neuropathy, ischemic 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.
diabetes mellitus type ii; diabetes mellitus, type 2; glucose metabolism disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; glucose metabolism disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; puerperal disorders; pulmonary embolism; pulmonary embolisms; thromboembolism; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; puerperal disorders; pulmonary embolism; pulmonary embolisms; thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sensation disorders; vestibular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease sensation disorders; vestibular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
migraine disorders; migraine with aura; migraine without aura; tension-type headache Gene Set From GAD Gene-Disease Associations genes associated with the disease migraine disorders; migraine with aura; migraine without aura; tension-type headache in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
major mood disorders: bipolar, major depression Gene Set From GAD Gene-Disease Associations genes associated with the disease major mood disorders: bipolar, major depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arteriosclerosis; brain ischemia; carotid artery diseases; cerebrovascular disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease arteriosclerosis; brain ischemia; carotid artery diseases; cerebrovascular disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy; migraine disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy; migraine disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders, inherited; pulmonary embolism; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited; pulmonary embolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; chromosome deletion; dystonic disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; chromosome deletion; dystonic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cocaine-related disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease cocaine-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal nutrition disorders; hypercholesterolemia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal nutrition disorders; hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebrovascular disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebrovascular disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular disease; lipid metabolism disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular disease; lipid metabolism disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hepatolenticular degeneration; movement disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease hepatolenticular degeneration; movement disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carotid artery diseases; cerebrovascular disorders; stroke; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease carotid artery diseases; cerebrovascular disorders; stroke; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia, myeloid, acute; leukemia, myelomonocytic, chronic; myeloproliferative disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, myeloid, acute; leukemia, myelomonocytic, chronic; myeloproliferative disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholism; disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholism; disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; cerebrovascular disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; cerebrovascular disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asbestos-associated pulmonary disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease asbestos-associated pulmonary disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
affective disorders/ suicide Gene Set From GAD Gene-Disease Associations genes associated with the disease affective disorders/ suicide in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dementia; memory disorders; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease dementia; memory disorders; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; pregnancy complications; puerperal disorders; recurrence; rheumatoid arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; pregnancy complications; puerperal disorders; recurrence; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dementia; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
genomic instability; myeloproliferative disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease genomic instability; myeloproliferative disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia, myeloid, acute; myelodysplastic syndromes; myeloproliferative disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, myeloid, acute; myelodysplastic syndromes; myeloproliferative disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arterial occlusive diseases; myeloproliferative disorders; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease arterial occlusive diseases; myeloproliferative disorders; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dyskinesia, drug-induced; movement disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease dyskinesia, drug-induced; movement disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
degenerative arthropathy ; facial pain; osteoarthritis; temporomandibular joint disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease degenerative arthropathy ; facial pain; osteoarthritis; temporomandibular joint disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetic neuropathies; peripheral nervous system diseases; sensation disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetic neuropathies; peripheral nervous system diseases; sensation disorders 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.
child nutrition disorders; cystic fibrosis; pseudomonas infections; respiratory tract infections Gene Set From GAD Gene-Disease Associations genes associated with the disease child nutrition disorders; cystic fibrosis; pseudomonas infections; respiratory tract infections 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.
epstein-barr virus infections; lymphoproliferative disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease epstein-barr virus infections; lymphoproliferative disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; olfaction disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; olfaction disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; cerebrovascular disorders; myocardial ischemia Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; cerebrovascular disorders; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; cerebrovascular disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; cerebrovascular disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
psychoses, substance-induced; substance-related disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease psychoses, substance-induced; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain infarction; brain ischemia; cerebrovascular disorders; hypertension; leukoaraiosis Gene Set From GAD Gene-Disease Associations genes associated with the disease brain infarction; brain ischemia; cerebrovascular disorders; hypertension; leukoaraiosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
biliary calculi; cholecystolithiasis; gallstones; lipid metabolism disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease biliary calculi; cholecystolithiasis; gallstones; lipid metabolism disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemoglobin disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease hemoglobin disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; prenatal exposure delayed effects; substance-related disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; prenatal exposure delayed effects; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pregnancy complications; tic disorder; tic disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease pregnancy complications; tic disorder; tic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
physiological sexual disorders; sexual dysfunction, physiological Gene Set From GAD Gene-Disease Associations genes associated with the disease physiological sexual disorders; sexual dysfunction, physiological in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholism; substance-related disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholism; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
photosensitivity disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease photosensitivity disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
migraine disorders; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease migraine disorders; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders; inflammation; nervous system diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; inflammation; nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mouth neoplasms; substance-related disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease mouth neoplasms; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
perceptual disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease perceptual disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
exfoliation syndrome; glaucoma, open-angle; pigmentation disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease exfoliation syndrome; glaucoma, open-angle; pigmentation disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
malignant myeloid disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease malignant myeloid disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
photosensitivity disorders; prurigo Gene Set From GAD Gene-Disease Associations genes associated with the disease photosensitivity disorders; prurigo in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep disorders, circadian rhythm Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep disorders, circadian rhythm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
substance-related disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
metabolism disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease metabolism disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; migraine disorders; myocardial infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; migraine disorders; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
learning disorders; multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease learning disorders; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; intracranial thrombosis; ischemic attack, transient; migraine disorders; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; intracranial thrombosis; ischemic attack, transient; migraine disorders; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders, inherited; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholism; cocaine-related disorders; substance withdrawal syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholism; cocaine-related disorders; substance withdrawal syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amphetamine-related disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease amphetamine-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
growth disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease growth disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
parkinson's disease; sleep disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease parkinson's disease; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neurodevelopmental psychiatric disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease neurodevelopmental psychiatric disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
opioid-related disorders; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease opioid-related disorders; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
language development disorders; mental retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease language development disorders; mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myeloproliferative disorders; polycythemia; polycythemia vera; thrombocythemia, essential; thrombocytosis Gene Set From GAD Gene-Disease Associations genes associated with the disease myeloproliferative disorders; polycythemia; polycythemia vera; thrombocythemia, essential; thrombocytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lipid metabolism disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease lipid metabolism disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep disorders; body mass Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep disorders; body mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amphetamine-related disorders; brain diseases, metabolic Gene Set From GAD Gene-Disease Associations genes associated with the disease amphetamine-related disorders; brain diseases, metabolic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
migraine disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease migraine disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
age-related skeletal disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease age-related skeletal disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
opioid-related disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease opioid-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
frontotemporal dementia; movement disorders; progressive supranuclear palsy; supranuclear palsy, progressive Gene Set From GAD Gene-Disease Associations genes associated with the disease frontotemporal dementia; movement disorders; progressive supranuclear palsy; supranuclear palsy, progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hiv infections; neuritis; somatosensory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease hiv infections; neuritis; somatosensory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cocaine-related disorders; Gene Set From GAD Gene-Disease Associations genes associated with the disease cocaine-related disorders; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders; osteonecrosis; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; osteonecrosis; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cadasil; cardiovascular diseases; hypertension; migraine disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease cadasil; cardiovascular diseases; hypertension; migraine disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glaucoma, open-angle; vision disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease glaucoma, open-angle; vision disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heroin dependence; substance-related disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease heroin dependence; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amphetamine-related disorders; psychoses, substance-induced Gene Set From GAD Gene-Disease Associations genes associated with the disease amphetamine-related disorders; psychoses, substance-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
folic acid deficiency; pregnancy complications; prenatal exposure delayed effects; psychomotor disorders; vitamin b 12 deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease folic acid deficiency; pregnancy complications; prenatal exposure delayed effects; psychomotor disorders; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hearing disorders; hearing loss, high-frequency; hearing problem Gene Set From GAD Gene-Disease Associations genes associated with the disease hearing disorders; hearing loss, high-frequency; hearing problem in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fragile x syndrome; fragile x syndromes; movement disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease fragile x syndrome; fragile x syndromes; movement disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
disorders of excessive somnolence; narcolepsy Gene Set From GAD Gene-Disease Associations genes associated with the disease disorders of excessive somnolence; narcolepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
major psychiatric disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease major psychiatric disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mental disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease mental disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neuroblastoma; substance-related disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease neuroblastoma; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis, coronary; lipid metabolism disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis, coronary; lipid metabolism disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dystonic disorders; Gene Set From GAD Gene-Disease Associations genes associated with the disease dystonic disorders; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myeloproliferative disorders; thrombophilia; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease myeloproliferative disorders; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myeloproliferative disorders; polycythemia vera; primary myelofibrosis; thrombocythemia, essential Gene Set From GAD Gene-Disease Associations genes associated with the disease myeloproliferative disorders; polycythemia vera; primary myelofibrosis; thrombocythemia, essential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; memory disorders; neurodegenerative diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; memory disorders; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcohol-induced disorders; esophageal neoplasms; liver cirrhosis, alcoholic; oesophageal neoplasm; pancreatitis, alcoholic Gene Set From GAD Gene-Disease Associations genes associated with the disease alcohol-induced disorders; esophageal neoplasms; liver cirrhosis, alcoholic; oesophageal neoplasm; pancreatitis, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenocarcinoma; carcinoma; hematologic neoplasms; hemochromatosis; myeloproliferative disorders; neoplasms; neoplasms, multiple primary Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma; hematologic neoplasms; hemochromatosis; myeloproliferative disorders; neoplasms; neoplasms, multiple primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lupus erythematosus, systemic; photosensitivity disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease lupus erythematosus, systemic; photosensitivity disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; central nervous system diseases; parkinson disease; parkinsonian disorders; spinocerebellar ataxias Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; central nervous system diseases; parkinson disease; parkinsonian disorders; spinocerebellar ataxias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amnesia; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease amnesia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anoxia; blood coagulation disorders, inherited; heart defects, congenital; infection; polycythemia; postoperative complications; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease anoxia; blood coagulation disorders, inherited; heart defects, congenital; infection; polycythemia; postoperative complications; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hematologic neoplasms; myeloproliferative disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease hematologic neoplasms; myeloproliferative disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
opioid-related disorders; substance withdrawal syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease opioid-related disorders; substance withdrawal syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain injuries; fatigue; sleep disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease brain injuries; fatigue; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
puerperal disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease puerperal disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; blood coagulation disorders, inherited; femur head necrosis; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; blood coagulation disorders, inherited; femur head necrosis; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemiplegia; migraine disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease hemiplegia; migraine disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
puerperal disorders; sinus thrombosis, intracranial Gene Set From GAD Gene-Disease Associations genes associated with the disease puerperal disorders; sinus thrombosis, intracranial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lipid metabolism disorders; muscular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease lipid metabolism disorders; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
memory disorders; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease memory disorders; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
emphysema; pulmonary disease, chronic obstructive; substance-related disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease emphysema; pulmonary disease, chronic obstructive; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome disorders; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome disorders; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus type ii; diabetes mellitus, type 2; hearing disorders; hearing problem Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hearing disorders; hearing problem in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hearing disorders; hearing problem; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease hearing disorders; hearing problem; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myotonic disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease myotonic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
parkinsonian disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease parkinsonian disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hot flashes; osteoporosis, postmenopausal; sleep disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease hot flashes; osteoporosis, postmenopausal; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dystonic disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease dystonic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperhomocysteinemia; lewy body disease; psychomotor disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; lewy body disease; psychomotor disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
tumor progression of bcr/abl negative chronic myeloproliferative disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease tumor progression of bcr/abl negative chronic myeloproliferative disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders, inherited; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; cadasil; migraine disorders; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; cadasil; migraine disorders; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune diseases; lymphoma; lymphoproliferative disorders; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; lymphoma; lymphoproliferative disorders; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gastrointestinal disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease gastrointestinal disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lymphoproliferative disorders; blood transfusion complications Gene Set From GAD Gene-Disease Associations genes associated with the disease lymphoproliferative disorders; blood transfusion complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
movement disorders; rett syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease movement disorders; rett syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
severe hyperkinetic disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease severe hyperkinetic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
temporomandibular joint disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease temporomandibular joint disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amphetamine-related disorders; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease amphetamine-related disorders; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome disorders; myotonic dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome disorders; myotonic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mood disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease mood disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, temporal lobe; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, temporal lobe; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
rheumatoid arthritis; hiv; rheiter's syndrome; urogenital disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease rheumatoid arthritis; hiv; rheiter's syndrome; urogenital disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; cerebrovascular disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cerebrovascular disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholism; marijuana abuse; substance-related disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholism; marijuana abuse; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep disorders; depressive disorder, major Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep disorders; depressive disorder, major in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myeloproliferative disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease myeloproliferative disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ciliary dyskinesias; ciliary motility disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease ciliary dyskinesias; ciliary motility disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep disorders; tourette syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep disorders; tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
tic disorder; tic disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease tic disorder; tic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep disorders; schizophrenia; body mass Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep disorders; schizophrenia; body mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; cystic fibrosis; growth disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; cystic fibrosis; growth disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; migraine disorders; neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; migraine disorders; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
respiration disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease respiration disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
migraine disorders; syndrome; vomiting Gene Set From GAD Gene-Disease Associations genes associated with the disease migraine disorders; syndrome; vomiting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; dementia; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hearing disorders; hearing problem Gene Set From GAD Gene-Disease Associations genes associated with the disease hearing disorders; hearing problem in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood platelet disorders; cardiovascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease blood platelet disorders; cardiovascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pain; temporomandibular joint disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease pain; temporomandibular joint disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amphetamine-related disorders; Gene Set From GAD Gene-Disease Associations genes associated with the disease amphetamine-related disorders; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
suicide; personality disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease suicide; personality disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myeloproliferative disorders; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease myeloproliferative disorders; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; psychomotor disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; psychomotor disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neurotic disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease neurotic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myeloproliferative disorders; thrombocytosis Gene Set From GAD Gene-Disease Associations genes associated with the disease myeloproliferative disorders; thrombocytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
memory disorders; sleep apnea syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease memory disorders; sleep apnea syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
intracranial embolism; migraine disorders; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease intracranial embolism; migraine disorders; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
digeorge syndrome; memory disorders; pharyngeal pouch; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease digeorge syndrome; memory disorders; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; mouth neoplasms; papillomavirus infections; squamous cell carcinoma; substance-related disorders; tumor virus infections Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; mouth neoplasms; papillomavirus infections; squamous cell carcinoma; substance-related disorders; tumor virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus type ii; diabetes mellitus, type 2; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heat stress disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease heat stress disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
budd-chiari syndrome; myeloproliferative disorders; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease budd-chiari syndrome; myeloproliferative disorders; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cumulative trauma disorders; occupational diseases; osteoarthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease cumulative trauma disorders; occupational diseases; osteoarthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; disease susceptibility; substance-related disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; disease susceptibility; substance-related disorders 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.
depressive disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease depressive disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
iron overload; myeloproliferative disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease iron overload; myeloproliferative disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aphasia, primary progressive; heredodegenerative disorders, nervous system Gene Set From GAD Gene-Disease Associations genes associated with the disease aphasia, primary progressive; heredodegenerative disorders, nervous system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coagulation protein disorders; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease coagulation protein disorders; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyotrophic lateral sclerosis; dementia; parkinsonian disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease amyotrophic lateral sclerosis; dementia; parkinsonian disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anxiety disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease anxiety disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
several psychiatric disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease several psychiatric disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lupus erythematosus, cutaneous; lupus erythematosus, discoid; photosensitivity disorders; skin diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease lupus erythematosus, cutaneous; lupus erythematosus, discoid; photosensitivity disorders; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gastritis; glucose metabolism disorders; helicobacter infections; stomach neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease gastritis; glucose metabolism disorders; helicobacter infections; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; carotid artery diseases; cerebrovascular disorders; hypertension Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; carotid artery diseases; cerebrovascular disorders; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lipid disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease lipid disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain injuries; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease brain injuries; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; down syndrome; olfaction disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; down syndrome; olfaction disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperhomocysteinemia; myeloproliferative disorders; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; myeloproliferative disorders; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; migraine disorders; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; migraine disorders; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; pregnancy complications, hematologic; puerperal disorders; pulmonary embolism; thrombophilia; thrombophlebitis; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; pregnancy complications, hematologic; puerperal disorders; pulmonary embolism; thrombophilia; thrombophlebitis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
paralysis; sensation disorders; spinal cord injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease paralysis; sensation disorders; spinal cord injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fatigue; neoplasms; sleep disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease fatigue; neoplasms; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hepatitis c, chronic; substance-related disorders; viremia Gene Set From GAD Gene-Disease Associations genes associated with the disease hepatitis c, chronic; substance-related disorders; viremia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
calcium metabolism disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease calcium metabolism disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
azoospermia; chromosome deletion; infertility, male; oligospermia; sex chromosome aberrations; sex chromosome disorders of sex development Gene Set From GAD Gene-Disease Associations genes associated with the disease azoospermia; chromosome deletion; infertility, male; oligospermia; sex chromosome aberrations; sex chromosome disorders of sex development in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; dementia; dementia, vascular; lipid metabolism disorders; neurodegenerative diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; dementia; dementia, vascular; lipid metabolism disorders; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glucose metabolism disorders; obesity; spinal dysraphism Gene Set From GAD Gene-Disease Associations genes associated with the disease glucose metabolism disorders; obesity; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
growth disorders; noonan syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease growth disorders; noonan syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; atrophy; dementia; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
psychotic disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease psychotic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
inflammation; migraine disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease inflammation; migraine disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
learning disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease learning disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lipid metabolism disorders; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease lipid metabolism disorders; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
memory disorders; prenatal exposure delayed effects Gene Set From GAD Gene-Disease Associations genes associated with the disease memory disorders; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hearing disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease hearing disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia, lymphocytic, chronic, b-cell; lymphoproliferative disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, lymphocytic, chronic, b-cell; lymphoproliferative disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders; legg-perthes disease; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; legg-perthes disease; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood-onset mood disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood-onset mood disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glucose metabolism disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease glucose metabolism disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dyskinesia, drug-induced; parkinsonian disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease dyskinesia, drug-induced; parkinsonian disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; migraine disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; migraine disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders, inherited; hypertension, pulmonary; pulmonary embolism Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited; hypertension, pulmonary; pulmonary embolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcohol-induced disorders, nervous system; alcoholism Gene Set From GAD Gene-Disease Associations genes associated with the disease alcohol-induced disorders, nervous system; alcoholism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lymphoproliferative disorders; myelodysplastic syndromes Gene Set From GAD Gene-Disease Associations genes associated with the disease lymphoproliferative disorders; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
migraine disorders(c10.228.140.546.399.750)/genetics Gene Set From GAD Gene-Disease Associations genes associated with the disease migraine disorders(c10.228.140.546.399.750)/genetics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcohol-induced disorders; esophageal neoplasms; laryngeal neoplasms; oropharyngeal neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease alcohol-induced disorders; esophageal neoplasms; laryngeal neoplasms; oropharyngeal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; dementia; hypothyroidism; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; dementia; hypothyroidism; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bipolar disorder ; mood disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease bipolar disorder ; mood disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, sickle cell; beta thalassemia; beta-thalassemia; blood coagulation disorders, inherited; sickle cell anemia; vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, sickle cell; beta thalassemia; beta-thalassemia; blood coagulation disorders, inherited; sickle cell anemia; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
migraine disorders; migraine with aura; migraine without aura Gene Set From GAD Gene-Disease Associations genes associated with the disease migraine disorders; migraine with aura; migraine without aura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
puerperal disorders; sinus thrombosis, intracranial; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease puerperal disorders; sinus thrombosis, intracranial; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
common variable immunodeficiency; lymphoproliferative disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease common variable immunodeficiency; lymphoproliferative disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; dementia; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders, inherited Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcohol-related disorders; alcoholism Gene Set From GAD Gene-Disease Associations genes associated with the disease alcohol-related disorders; alcoholism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyotrophic lateral sclerosis; frontotemporal dementia; parkinsonian disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease amyotrophic lateral sclerosis; frontotemporal dementia; parkinsonian disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebrovascular disorders; Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebrovascular disorders; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; brain infarction; cerebrovascular disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; brain infarction; cerebrovascular disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myeloproliferative disorders; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease myeloproliferative disorders; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemochromatosis; iron metabolism disorders; iron overload Gene Set From GAD Gene-Disease Associations genes associated with the disease hemochromatosis; iron metabolism disorders; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholesterol, ldl; insulin; metabolism disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease cholesterol, ldl; insulin; metabolism disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; olfaction disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; olfaction disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
agricultural workers' diseases; dna damage; substance-related disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease agricultural workers' diseases; dna damage; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronobiology disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease chronobiology disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital megacolon; hirschsprung disease; urea cycle disorders, inborn Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital megacolon; hirschsprung disease; urea cycle disorders, inborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcohol-induced disorders; prenatal exposure delayed effects Gene Set From GAD Gene-Disease Associations genes associated with the disease alcohol-induced disorders; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral hemorrhage; cerebral hemorrhages; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral hemorrhage; cerebral hemorrhages; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep disorders; body mass; blood pressure, arterial Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep disorders; body mass; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blepharospasm; dystonia; dystonic disorders; torticollis Gene Set From GAD Gene-Disease Associations genes associated with the disease blepharospasm; dystonia; dystonic disorders; torticollis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
headache; migraine disorders; neurogenic inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease headache; migraine disorders; neurogenic inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
substance withdrawal syndrome; substance-related disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease substance withdrawal syndrome; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myeloproliferative disorders; polycythemia vera Gene Set From GAD Gene-Disease Associations genes associated with the disease myeloproliferative disorders; polycythemia vera in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebrovascular disorders; foramen ovale, patent; hyperhomocysteinemia; hypertension Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebrovascular disorders; foramen ovale, patent; hyperhomocysteinemia; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
growth disorders; puberty, delayed Gene Set From GAD Gene-Disease Associations genes associated with the disease growth disorders; puberty, delayed in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
psychiatric disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease psychiatric disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholism; sleep disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholism; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
metabolic diseases; migraine disorders; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease metabolic diseases; migraine disorders; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune diseases; lymphoproliferative disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; lymphoproliferative disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; growth disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; growth disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic diseases; autoimmune diseases; chorea; choreatic disorders; myocarditis; rheumatic heart disease; streptococcal infections Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic diseases; autoimmune diseases; chorea; choreatic disorders; myocarditis; rheumatic heart disease; streptococcal infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
inflammation; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease inflammation; memory disorders 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.
budd-chiari syndrome; myeloproliferative disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease budd-chiari syndrome; myeloproliferative disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; cerebrovascular disorders; ischemic attack, transient; recurrence; stroke; transient ischemic attack Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; cerebrovascular disorders; ischemic attack, transient; recurrence; stroke; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
digeorge syndrome; ocular motility disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease digeorge syndrome; ocular motility disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; congenital heart defects; growth disorders; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; congenital heart defects; growth disorders; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lymphoproliferative disorders; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease lymphoproliferative disorders; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dementia; olfaction disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease dementia; olfaction disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lymphocytosis; lymphoproliferative disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease lymphocytosis; lymphoproliferative disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myeloproliferative disorders; neoplasms; venous thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease myeloproliferative disorders; neoplasms; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
movement disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease movement disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia, myelogenous, chronic, bcr-abl positive; myelodysplastic syndromes; myeloproliferative disorders; polycythemia vera; precursor cell lymphoblastic leukemia-lymphoma; thrombocythemia, essential Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, myelogenous, chronic, bcr-abl positive; myelodysplastic syndromes; myeloproliferative disorders; polycythemia vera; precursor cell lymphoblastic leukemia-lymphoma; thrombocythemia, essential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholism; cocaine-related disorders; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholism; cocaine-related disorders; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarct; lymphoproliferative disorders; restenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarct; lymphoproliferative disorders; restenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; memory disorders; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; memory disorders; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
iron metabolism disorders; iron overload Gene Set From GAD Gene-Disease Associations genes associated with the disease iron metabolism disorders; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lysosomal storage disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease lysosomal storage disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemochromatosis; iron overload; pigmentation disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease hemochromatosis; iron overload; pigmentation disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; chromosome breakage; facies; growth disorders; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; chromosome breakage; facies; growth disorders; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
personality disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease personality disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apraxias; hearing loss, sensorineural; language development disorders; mutism; sensorineural hearing loss Gene Set From GAD Gene-Disease Associations genes associated with the disease apraxias; hearing loss, sensorineural; language development disorders; mutism; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
disorders of excessive somnolence; Gene Set From GAD Gene-Disease Associations genes associated with the disease disorders of excessive somnolence; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
psychotic symptoms in mood disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease psychotic symptoms in mood disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myeloproliferative disorders; neovascularization, pathologic Gene Set From GAD Gene-Disease Associations genes associated with the disease myeloproliferative disorders; neovascularization, pathologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lymphoproliferative disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease lymphoproliferative disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus; hearing disorders; hearing problem; mitochondrial diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; hearing disorders; hearing problem; mitochondrial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dystonia; psychomotor disorders; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease dystonia; psychomotor disorders; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
language development disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease language development disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lupus erythematosus, cutaneous; photosensitivity disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease lupus erythematosus, cutaneous; photosensitivity disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholism; cocaine-related disorders; Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholism; cocaine-related disorders; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcohol-related disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alcohol-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cumulative trauma disorders; rhabdomyolysis Gene Set From GAD Gene-Disease Associations genes associated with the disease cumulative trauma disorders; rhabdomyolysis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
degenerative arthropathy ; osteoarthritis; temporomandibular joint disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease degenerative arthropathy ; osteoarthritis; temporomandibular joint disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
disorders of excessive somnolence; fatigue; gastrointestinal diseases; respiratory tract infections; rhinitis; urticaria; xerostomia Gene Set From GAD Gene-Disease Associations genes associated with the disease disorders of excessive somnolence; fatigue; gastrointestinal diseases; respiratory tract infections; rhinitis; urticaria; xerostomia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
eating disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease eating disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
opioid-related disorders; pain Gene Set From GAD Gene-Disease Associations genes associated with the disease opioid-related disorders; pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lymphoproliferative disorders; multiple myeloma Gene Set From GAD Gene-Disease Associations genes associated with the disease lymphoproliferative disorders; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myeloproliferative disorders; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease myeloproliferative disorders; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular disorders, atrophic Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular disorders, atrophic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
deglutition disorders; muscle weakness; myositis, inclusion body Gene Set From GAD Gene-Disease Associations genes associated with the disease deglutition disorders; muscle weakness; myositis, inclusion body in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abortion, spontaneous; abruptio placentae; blood coagulation disorders, inherited; pregnancy complications, hematologic; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease abortion, spontaneous; abruptio placentae; blood coagulation disorders, inherited; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myeloproliferative disorders; polycythemia vera; thrombocythemia, essential Gene Set From GAD Gene-Disease Associations genes associated with the disease myeloproliferative disorders; polycythemia vera; thrombocythemia, essential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myelodysplastic syndromes; myeloproliferative disorders; preleukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease myelodysplastic syndromes; myeloproliferative disorders; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
46, xx disorders of sex development; pof - premature ovarian failure; primary ovarian insufficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease 46, xx disorders of sex development; pof - premature ovarian failure; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders; eclampsia; hellp syndrome; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; eclampsia; hellp syndrome; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
psychophysiologic disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease psychophysiologic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic progressive chorea; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic progressive chorea; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; cerebrovascular disorders; dementia, vascular Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cerebrovascular disorders; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
metabolism disorders; myocardial infarction; stroke, ischemic Gene Set From GAD Gene-Disease Associations genes associated with the disease metabolism disorders; myocardial infarction; stroke, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia ; mood disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia ; mood disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
puerperal disorders; sepsis; streptococcal infections; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease puerperal disorders; sepsis; streptococcal infections; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blast crisis; blast phase; myeloproliferative disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease blast crisis; blast phase; myeloproliferative disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dystonic disorders; multiple system atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease dystonic disorders; multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders, inherited; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
suicide ; mood disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease suicide ; mood disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebrovascular disorders; myocardial ischemia Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebrovascular disorders; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; fetal diseases; nutrition disorders; osteoporosis; prenatal exposure delayed effects Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; fetal diseases; nutrition disorders; osteoporosis; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; beta-thalassemia; blood coagulation disorders; thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; beta-thalassemia; blood coagulation disorders; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis, coronary; metabolism disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis, coronary; metabolism disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lipid metabolism disorders; hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease lipid metabolism disorders; hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; migraine disorders; migraine with aura Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; migraine disorders; migraine with aura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
memory disorders; mercury poisoning, nervous system; occupational diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease memory disorders; mercury poisoning, nervous system; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
growth disorders; weight gain Gene Set From GAD Gene-Disease Associations genes associated with the disease growth disorders; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
disorders Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term disorders in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
GLO1_OE_GDS4991_546_mouse_anxiety disorders Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the GLO1_OE_GDS4991_546_mouse_anxiety disorders gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
Eating disorders (purging via substances) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Eating disorders (purging via substances) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Temporomandibular joint disorders Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Temporomandibular joint disorders phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Eating disorders Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Eating disorders phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Major mood disorders Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Major mood disorders phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
dermatological manifestations of systemic disorders Gene Set From GWASdb SNP-Phenotype Associations genes associated with the dermatological manifestations of systemic disorders phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
dermatological manifestations of systemic disorders Gene Set From HPO Gene-Disease Associations genes associated with the dermatological manifestations of systemic disorders phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Sex Chromosome Disorders of Sex Development Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sex Chromosome Disorders of Sex Development phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Child Development Disorders, Pervasive Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Child Development Disorders, Pervasive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Opioid-Related Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Opioid-Related Disorders 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.
Language Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Language Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Stress Disorders, Traumatic, Acute Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Stress Disorders, Traumatic, Acute phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Child Behavior Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Child Behavior Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Movement Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Movement Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Language Development Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Language Development Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Chronobiology Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Chronobiology Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Olfaction Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Olfaction Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Child Nutrition Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Child Nutrition Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sleep Disorders, Circadian Rhythm Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep Disorders, Circadian Rhythm phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Adjustment Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Adjustment Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Mood Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Mood Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Alcohol-Related Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Alcohol-Related Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Alcohol-Induced Disorders, Nervous System Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Alcohol-Induced Disorders, Nervous System phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cognition Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cognition Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Myotonic Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Myotonic Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Hemostatic Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hemostatic Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Iron Metabolism Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Iron Metabolism Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Muscular Disorders, Atrophic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Disorders, Atrophic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Anxiety Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Anxiety Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Phobic Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Phobic Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Somatoform Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Somatoform Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
46, XY Disorders of Sex Development Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the 46, XY Disorders of Sex Development phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sleep Arousal Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep Arousal Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Mental Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Mental Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Affective Disorders, Psychotic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Affective Disorders, Psychotic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Paranoid Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Paranoid Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Nutrition Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Nutrition Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Learning Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Learning Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Growth Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Growth Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Stress Disorders, Post-Traumatic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Stress Disorders, Post-Traumatic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Vision Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Vision Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Neurotic Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Neurotic Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Respiration Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Respiration Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Taste Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Taste Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Hearing Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hearing Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Voice Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Voice Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Urea Cycle Disorders, Inborn Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Urea Cycle Disorders, Inborn phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Coagulation Protein Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Coagulation Protein Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Temporomandibular Joint Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Temporomandibular Joint Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Photosensitivity Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Photosensitivity Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Alcohol-Induced Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Alcohol-Induced Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cocaine-Related Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cocaine-Related Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Myeloproliferative Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Myeloproliferative Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Disorders of Excessive Somnolence Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Disorders of Excessive Somnolence phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Substance-Related Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Substance-Related Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Combat Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Combat Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Psychophysiologic Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Psychophysiologic Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Speech Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Speech Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Articulation Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Articulation Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Congenital Disorders of Glycosylation Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Congenital Disorders of Glycosylation phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Auditory Perceptual Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Auditory Perceptual Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Lipid Metabolism Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Lipid Metabolism Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Leukocyte Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Leukocyte Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Chromosome Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Chromosome Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Motor Skills Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Motor Skills Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Memory Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Memory Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Blood Coagulation Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Blood Coagulation Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Blood Platelet Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Blood Platelet Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Choreatic Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Choreatic Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Glucose Metabolism Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Glucose Metabolism Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Ocular Motility Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Ocular Motility Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Delirium, Dementia, Amnestic, Cognitive Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Delirium, Dementia, Amnestic, Cognitive Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Impulse Control Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Impulse Control Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Headache Disorders, Secondary Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Headache Disorders, Secondary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Migraine Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Migraine Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sensation Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sensation Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Pigmentation Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Pigmentation Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Lymphoproliferative Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Lymphoproliferative Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Dissociative Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Dissociative Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Puerperal Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Puerperal Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Eating Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Eating Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Urination Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Urination Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Psychomotor Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Psychomotor Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Personality Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Personality Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Ciliary Motility Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Ciliary Motility Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
46, XX Disorders of Sex Development Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the 46, XX Disorders of Sex Development phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Amphetamine-Related Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Amphetamine-Related Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Gait Disorders, Neurologic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Gait Disorders, Neurologic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Perceptual Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Perceptual Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Psychotic Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Psychotic Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Heredodegenerative Disorders, Nervous System Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Heredodegenerative Disorders, Nervous System phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Communication Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Communication Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Tic Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Tic Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Dystonic Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Dystonic Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Blood Coagulation Disorders, Inherited Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Blood Coagulation Disorders, Inherited phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Headache Disorders, Primary Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Headache Disorders, Primary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cerebrovascular Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cerebrovascular Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sleep Disorders, Intrinsic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep Disorders, Intrinsic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
DNA Repair-Deficiency Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the DNA Repair-Deficiency Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sleep Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sleep Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Parkinsonian Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Parkinsonian Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Stress Disorders, Traumatic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Stress Disorders, Traumatic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Heat Stress Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Heat Stress Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Disorders of Sex Development Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Disorders of Sex Development phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Fetal Nutrition Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Fetal Nutrition Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Calcium Metabolism Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Calcium Metabolism Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cumulative Trauma Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cumulative Trauma Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
disorders Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term disorders in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
Metabolic disorders of biological oxidation enzymes Gene Set From Reactome Pathways 2014 proteins participating in the Metabolic disorders of biological oxidation enzymes pathway from the Reactome Pathways dataset.
Nonorganic Sleep Wake Cycle Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nonorganic Sleep Wake Cycle Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mental Disorders, Severe Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mental Disorders, Severe in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Functional Gastrointestinal Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Functional Gastrointestinal Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Organic Mental Disorders, Substance-Induced Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Organic Mental Disorders, Substance-Induced in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Memory Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Memory Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Protein Misfolding Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Protein Misfolding Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Circadian Rhythm Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Circadian Rhythm Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aqueous Humor Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aqueous Humor Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Combat Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Combat Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Amino Acid Metabolism, Inherited Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Amino Acid Metabolism, Inherited Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Alcohol-Induced Disorders, Nervous System Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Alcohol-Induced Disorders, Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cortex Bone Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cortex Bone Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Nervous System Metabolic Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Metabolic Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Speech Sound Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Speech Sound Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Phencyclidine-Related Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Phencyclidine-Related Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ecstasy Related Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ecstasy Related Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
46, Xx Disorders Of Sex Development Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease 46, Xx Disorders Of Sex Development in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Other Disorders Of Branched-Chain Amino-Acid Metabolism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Other Disorders Of Branched-Chain Amino-Acid Metabolism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Feeding Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Feeding Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pediatric Autoimmune Neuropsychiatric Disorders Associated With Streptococcal Infections Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pediatric Autoimmune Neuropsychiatric Disorders Associated With Streptococcal Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lenticulostriate Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lenticulostriate Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ovotesticular Disorders Of Sex Development Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ovotesticular Disorders Of Sex Development in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Tic Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Tic Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Motor Tic Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Motor Tic Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tic Disorders, Vocal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tic Disorders, Vocal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pelvic Floor Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pelvic Floor Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Immune Disorders, Nervous System Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Immune Disorders, Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Eye Disorders (Excl Glaucoma) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Eye Disorders (Excl Glaucoma) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Other Alcohol-Induced Mental Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Other Alcohol-Induced Mental Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Communication Disorders, Developmental Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Communication Disorders, Developmental in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Organic Mental Disorders, Psychotic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Organic Mental Disorders, Psychotic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Gait Disorders, Neurologic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Gait Disorders, Neurologic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
46, Xy Disorders Of Sex Development Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease 46, Xy Disorders Of Sex Development in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Nutrition Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Nutrition Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sleep Disorders, Extrinsic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sleep Disorders, Extrinsic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Other Specified Disorders Of Adrenal Gland Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Other Specified Disorders Of Adrenal Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Other Disorders Of Lipoid Metabolism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Other Disorders Of Lipoid Metabolism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Articulation Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Articulation Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Headache Disorders, Primary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Headache Disorders, Primary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Heat Stress Disorders Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Heat Stress Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Consciousness Disorders Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Consciousness Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Dermatological Manifestations Of Systemic Disorders Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dermatological Manifestations Of Systemic Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Position Sense Disorders Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Position Sense Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Proprioceptive Disorders Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proprioceptive Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Thermal Sensation Disorders Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thermal Sensation Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Verbal Fluency Disorders Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Verbal Fluency Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Other Specified Conduction Disorders Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Other Specified Conduction Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Special Senses Disorders Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Special Senses Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Physiological Sexual Disorders Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Physiological Sexual Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neurotransmitter disorders Gene Set From WikiPathways Pathways 2024 proteins participating in the Neurotransmitter disorders pathway from the WikiPathways Pathways 2024 dataset.
Krebs cycle disorders Gene Set From WikiPathways Pathways 2024 proteins participating in the Krebs cycle disorders pathway from the WikiPathways Pathways 2024 dataset.
Vitamin B12 disorders Gene Set From WikiPathways Pathways 2024 proteins participating in the Vitamin B12 disorders pathway from the WikiPathways Pathways 2024 dataset.
Biomarkers for urea cycle disorders Gene Set From WikiPathways Pathways 2024 proteins participating in the Biomarkers for urea cycle disorders pathway from the WikiPathways Pathways 2024 dataset.
Biomarkers for pyrimidine metabolism disorders Gene Set From WikiPathways Pathways 2024 proteins participating in the Biomarkers for pyrimidine metabolism disorders pathway from the WikiPathways Pathways 2024 dataset.
Mitochondrial fatty acid oxidation disorders Gene Set From WikiPathways Pathways 2024 proteins participating in the Mitochondrial fatty acid oxidation disorders pathway from the WikiPathways Pathways 2024 dataset.
Iron metabolism disorders Gene Set From WikiPathways Pathways 2024 proteins participating in the Iron metabolism disorders pathway from the WikiPathways Pathways 2024 dataset.
Disorders of galactose metabolism Gene Set From WikiPathways Pathways 2024 proteins participating in the Disorders of galactose metabolism pathway from the WikiPathways Pathways 2024 dataset.
Disorders in ketone body synthesis Gene Set From WikiPathways Pathways 2024 proteins participating in the Disorders in ketone body synthesis pathway from the WikiPathways Pathways 2024 dataset.
Disorders of fructose metabolism Gene Set From WikiPathways Pathways 2024 proteins participating in the Disorders of fructose metabolism pathway from the WikiPathways Pathways 2024 dataset.
Cholesterol synthesis disorders Gene Set From WikiPathways Pathways 2024 proteins participating in the Cholesterol synthesis disorders pathway from the WikiPathways Pathways 2024 dataset.
Disorders in ketolysis Gene Set From WikiPathways Pathways 2024 proteins participating in the Disorders in ketolysis pathway from the WikiPathways Pathways 2024 dataset.
Metabolic epileptic disorders Gene Set From WikiPathways Pathways 2024 proteins participating in the Metabolic epileptic disorders pathway from the WikiPathways Pathways 2024 dataset.
ABC transporter disorders Gene Set From Reactome Pathways 2024 proteins participating in the ABC transporter disorders pathway from the Reactome Pathways 2024 dataset.
Disorders of Developmental Biology Gene Set From Reactome Pathways 2024 proteins participating in the Disorders of Developmental Biology pathway from the Reactome Pathways 2024 dataset.
Disorders of Nervous System Development Gene Set From Reactome Pathways 2024 proteins participating in the Disorders of Nervous System Development pathway from the Reactome Pathways 2024 dataset.
Disorders of transmembrane transporters Gene Set From Reactome Pathways 2024 proteins participating in the Disorders of transmembrane transporters pathway from the Reactome Pathways 2024 dataset.
Metabolic disorders of biological oxidation enzymes Gene Set From Reactome Pathways 2024 proteins participating in the Metabolic disorders of biological oxidation enzymes pathway from the Reactome Pathways 2024 dataset.
Pervasive developmental disorders Gene Set From Reactome Pathways 2024 proteins participating in the Pervasive developmental disorders pathway from the Reactome Pathways 2024 dataset.
SLC transporter disorders Gene Set From Reactome Pathways 2024 proteins participating in the SLC transporter disorders pathway from the Reactome Pathways 2024 dataset.
APC-Associated Polyposis Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the APC-Associated Polyposis Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Disorders of Intracellular Cobalamin Metabolism Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Disorders of Intracellular Cobalamin Metabolism phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
WFS1-Related Spectrum Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the WFS1-Related Spectrum Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
TRPV4-Associated Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the TRPV4-Associated Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
LARGE1-Related Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the LARGE1-Related Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
TP63-Related Spectrum Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the TP63-Related Spectrum Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Zellweger spectrum disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Zellweger spectrum disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
TUBB3-Releated Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the TUBB3-Releated Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
PMS2-related cancer disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the PMS2-related cancer disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
L1CAM-related disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the L1CAM-related disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
POLG-Related Spectrum Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the POLG-Related Spectrum Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
PIK3CA-Related Overgrowth Spectrum Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the PIK3CA-Related Overgrowth Spectrum Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Disorders of GNAS Inactivation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Disorders of GNAS Inactivation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
GGCX - Related Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the GGCX - Related Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
FLNB-Related Spectrum Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the FLNB-Related Spectrum Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
ASAH1-related disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the ASAH1-related disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
MTFMT-Related Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the MTFMT-Related Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
ERCC4-Related Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the ERCC4-Related Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
LARS2-Related Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the LARS2-Related Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
PRRT2-Associated Paroxysmal Movement Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the PRRT2-Associated Paroxysmal Movement Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
MAPT-Related Spectrum Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the MAPT-Related Spectrum Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SCN1A Seizure Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SCN1A Seizure Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
PPP2R1A-related neurodevelopmental disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the PPP2R1A-related neurodevelopmental disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
KIAA0586- Related disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the KIAA0586- Related disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital disorders of glycosylation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital disorders of glycosylation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
DYNC1H1-related neurodevelopmental disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the DYNC1H1-related neurodevelopmental disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Branchiootorenal Spectrum Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Branchiootorenal Spectrum Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ataxia Neuropathy Spectrum Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia Neuropathy Spectrum Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
KAT6B-Related Spectrum Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the KAT6B-Related Spectrum Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
CASR-related calcium metabolism disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the CASR-related calcium metabolism disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
POLR3A-related neurological disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the POLR3A-related neurological disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
CACNA1A-associated disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the CACNA1A-associated disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
CSF3R-Related Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the CSF3R-Related Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
ITPR1-related disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the ITPR1-related disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
RECQL4-related spectrum disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the RECQL4-related spectrum disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neurodevelopmental disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neurodevelopmental disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
MORC2-related neurodevelopmental disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the MORC2-related neurodevelopmental disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
ASH1L-related neurodevelopmental disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the ASH1L-related neurodevelopmental disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
PAK1-related neurodevelopmental disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the PAK1-related neurodevelopmental disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
POLG2-related spectrum disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the POLG2-related spectrum disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
CIC-related neurodevelopmental disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the CIC-related neurodevelopmental disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
NDUFB11-related disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the NDUFB11-related disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
HTRA2-Related Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the HTRA2-Related Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
COASY-Related Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the COASY-Related Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
F8-related disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the F8-related disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autism spectrum disorders (social interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Autism spectrum disorders (social interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Anxiety disorders Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Anxiety disorders phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Eating disorders Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Eating disorders phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Disorders of lipid metabolism Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Disorders of lipid metabolism phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Major mood disorders Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Major mood disorders phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Eating disorders (purging via substances) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Eating disorders (purging via substances) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Plantar fascial disorders Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Plantar fascial disorders phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Stress-related disorders Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Stress-related disorders phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Pursuit maintenance gain in psychotic disorders Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pursuit maintenance gain in psychotic disorders phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Initial pursuit acceleration in psychotic disorders Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Initial pursuit acceleration in psychotic disorders phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Anti-saccade error rate in psychotic disorders Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Anti-saccade error rate in psychotic disorders phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Suicide attempt severity in mood disorders Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Suicide attempt severity in mood disorders phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Suicidality in mood disorders Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Suicidality in mood disorders phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Basic cell groups and regions Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Basic cell groups and regions relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
head and face region of M1 Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in head and face region of M1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
telomeres telomerase cellular aging and immortality Gene Set From Biocarta Pathways proteins participating in the telomeres telomerase cellular aging and immortality pathway from the Biocarta Pathways dataset.
mcalpain and friends in cell motility Gene Set From Biocarta Pathways proteins participating in the mcalpain and friends in cell motility pathway from the Biocarta Pathways dataset.
role of ppar-gamma coactivators in obesity and thermogenesis Gene Set From Biocarta Pathways proteins participating in the role of ppar-gamma coactivators in obesity and thermogenesis pathway from the Biocarta Pathways dataset.
il12 and stat4 dependent signaling pathway in th1 development Gene Set From Biocarta Pathways proteins participating in the il12 and stat4 dependent signaling pathway in th1 development pathway from the Biocarta Pathways dataset.
hypoxia and p53 in the cardiovascular system Gene Set From Biocarta Pathways proteins participating in the hypoxia and p53 in the cardiovascular system pathway from the Biocarta Pathways dataset.
lissencephaly gene (lis1) in neuronal migration and development Gene Set From Biocarta Pathways proteins participating in the lissencephaly gene (lis1) in neuronal migration and development pathway from the Biocarta Pathways dataset.
role of erbb2 in signal transduction and oncology Gene Set From Biocarta Pathways proteins participating in the role of erbb2 in signal transduction and oncology pathway from the Biocarta Pathways dataset.
corticosteroids and cardioprotection Gene Set From Biocarta Pathways proteins participating in the corticosteroids and cardioprotection pathway from the Biocarta Pathways dataset.
cyclins and cell cycle regulation Gene Set From Biocarta Pathways proteins participating in the cyclins and cell cycle regulation pathway from the Biocarta Pathways dataset.
mechanism of acetaminophen activity and toxicity Gene Set From Biocarta Pathways proteins participating in the mechanism of acetaminophen activity and toxicity pathway from the Biocarta Pathways dataset.
nfat and hypertrophy of the heart Gene Set From Biocarta Pathways proteins participating in the nfat and hypertrophy of the heart pathway from the Biocarta Pathways dataset.
acetylation and deacetylation of rela in nucleus Gene Set From Biocarta Pathways proteins participating in the acetylation and deacetylation of rela in nucleus pathway from the Biocarta Pathways dataset.
thrombin signaling and protease-activated receptors Gene Set From Biocarta Pathways proteins participating in the thrombin signaling and protease-activated receptors pathway from the Biocarta Pathways dataset.
antigen processing and presentation Gene Set From Biocarta Pathways proteins participating in the antigen processing and presentation pathway from the Biocarta Pathways dataset.
stathmin and breast cancer resistance to antimicrotubule agents Gene Set From Biocarta Pathways proteins participating in the stathmin and breast cancer resistance to antimicrotubule agents pathway from the Biocarta Pathways dataset.
role of ß-arrestins in the activation and targeting of map kinases Gene Set From Biocarta Pathways proteins participating in the role of ß-arrestins in the activation and targeting of map kinases pathway from the Biocarta Pathways dataset.
cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway Gene Set From Biocarta Pathways proteins participating in the cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway pathway from the Biocarta Pathways dataset.
role of pi3k subunit p85 in regulation of actin organization and cell migration Gene Set From Biocarta Pathways proteins participating in the role of pi3k subunit p85 in regulation of actin organization and cell migration pathway from the Biocarta Pathways dataset.
btg family proteins and cell cycle regulation Gene Set From Biocarta Pathways proteins participating in the btg family proteins and cell cycle regulation pathway from the Biocarta Pathways dataset.
control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) Gene Set From Biocarta Pathways proteins participating in the control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) pathway from the Biocarta Pathways dataset.
endocytotic role of ndk phosphins and dynamin Gene Set From Biocarta Pathways proteins participating in the endocytotic role of ndk phosphins and dynamin pathway from the Biocarta Pathways dataset.
regulation of eif-4e and p70s6 kinase Gene Set From Biocarta Pathways proteins participating in the regulation of eif-4e and p70s6 kinase pathway from the Biocarta Pathways dataset.
estrogen responsive protein efp controls cell cycle and breast tumors growth Gene Set From Biocarta Pathways proteins participating in the estrogen responsive protein efp controls cell cycle and breast tumors growth pathway from the Biocarta Pathways dataset.
vegf hypoxia and angiogenesis Gene Set From Biocarta Pathways proteins participating in the vegf hypoxia and angiogenesis pathway from the Biocarta Pathways dataset.
yaci and bcma stimulation of b cell immune responses Gene Set From Biocarta Pathways proteins participating in the yaci and bcma stimulation of b cell immune responses pathway from the Biocarta Pathways dataset.
lck and fyn tyrosine kinases in initiation of tcr activation Gene Set From Biocarta Pathways proteins participating in the lck and fyn tyrosine kinases in initiation of tcr activation pathway from the Biocarta Pathways dataset.
hiv-1 nef: negative effector of fas and tnf Gene Set From Biocarta Pathways proteins participating in the hiv-1 nef: negative effector of fas and tnf pathway from the Biocarta Pathways dataset.
nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells Gene Set From Biocarta Pathways proteins participating in the nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells pathway from the Biocarta Pathways dataset.
ucalpain and friends in cell spread Gene Set From Biocarta Pathways proteins participating in the ucalpain and friends in cell spread pathway from the Biocarta Pathways dataset.
ionomycin and phorbal ester signaling pathway Gene Set From Biocarta Pathways proteins participating in the ionomycin and phorbal ester signaling pathway pathway from the Biocarta Pathways dataset.
carm1 and regulation of the estrogen receptor Gene Set From Biocarta Pathways proteins participating in the carm1 and regulation of the estrogen receptor pathway from the Biocarta Pathways dataset.
phosphoinositides and their downstream targets Gene Set From Biocarta Pathways proteins participating in the phosphoinositides and their downstream targets pathway from the Biocarta Pathways dataset.
melanocyte development and pigmentation pathway Gene Set From Biocarta Pathways proteins participating in the melanocyte development and pigmentation pathway pathway from the Biocarta Pathways dataset.
akap95 role in mitosis and chromosome dynamics Gene Set From Biocarta Pathways proteins participating in the akap95 role in mitosis and chromosome dynamics pathway from the Biocarta Pathways dataset.
transcription factor creb and its extracellular signals Gene Set From Biocarta Pathways proteins participating in the transcription factor creb and its extracellular signals pathway from the Biocarta Pathways dataset.
visceral fat deposits and the metabolic syndrome Gene Set From Biocarta Pathways proteins participating in the visceral fat deposits and the metabolic syndrome pathway from the Biocarta Pathways dataset.
the igf-1 receptor and longevity Gene Set From Biocarta Pathways proteins participating in the the igf-1 receptor and longevity pathway from the Biocarta Pathways dataset.
cdc25 and chk1 regulatory pathway in response to dna damage Gene Set From Biocarta Pathways proteins participating in the cdc25 and chk1 regulatory pathway in response to dna damage pathway from the Biocarta Pathways dataset.
human cytomegalovirus and map kinase pathways Gene Set From Biocarta Pathways proteins participating in the human cytomegalovirus and map kinase pathways pathway from the Biocarta Pathways dataset.
influence of ras and rho proteins on g1 to s transition Gene Set From Biocarta Pathways proteins participating in the influence of ras and rho proteins on g1 to s transition pathway from the Biocarta Pathways dataset.
proteolysis and signaling pathway of notch Gene Set From Biocarta Pathways proteins participating in the proteolysis and signaling pathway of notch pathway from the Biocarta Pathways dataset.
apoptotic dna-fragmentation and tissue homeostasis Gene Set From Biocarta Pathways proteins participating in the apoptotic dna-fragmentation and tissue homeostasis pathway from the Biocarta Pathways dataset.
ion channels and their functional role in vascular endothelium Gene Set From Biocarta Pathways proteins participating in the ion channels and their functional role in vascular endothelium pathway from the Biocarta Pathways dataset.
alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease Gene Set From Biocarta Pathways proteins participating in the alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease pathway from the Biocarta Pathways dataset.
fosb gene expression and drug abuse Gene Set From Biocarta Pathways proteins participating in the fosb gene expression and drug abuse pathway from the Biocarta Pathways dataset.
links between pyk2 and map kinases Gene Set From Biocarta Pathways proteins participating in the links between pyk2 and map kinases pathway from the Biocarta Pathways dataset.
opposing roles of aif in apoptosis and cell survival Gene Set From Biocarta Pathways proteins participating in the opposing roles of aif in apoptosis and cell survival pathway from the Biocarta Pathways dataset.
degradation of the rar and rxr by the proteasome Gene Set From Biocarta Pathways proteins participating in the degradation of the rar and rxr by the proteasome pathway from the Biocarta Pathways dataset.
cadmium induces dna synthesis and proliferation in macrophages Gene Set From Biocarta Pathways proteins participating in the cadmium induces dna synthesis and proliferation in macrophages pathway from the Biocarta Pathways dataset.
erk and pi-3 kinase are necessary for collagen binding in corneal epithelia Gene Set From Biocarta Pathways proteins participating in the erk and pi-3 kinase are necessary for collagen binding in corneal epithelia pathway from the Biocarta Pathways dataset.
role of brca1 brca2 and atr in cancer susceptibility Gene Set From Biocarta Pathways proteins participating in the role of brca1 brca2 and atr in cancer susceptibility pathway from the Biocarta Pathways dataset.
chrebp regulation by carbohydrates and camp Gene Set From Biocarta Pathways proteins participating in the chrebp regulation by carbohydrates and camp pathway from the Biocarta Pathways dataset.
pten dependent cell cycle arrest and apoptosis Gene Set From Biocarta Pathways proteins participating in the pten dependent cell cycle arrest and apoptosis pathway from the Biocarta Pathways dataset.
induction of apoptosis through dr3 and dr4/5 death receptors Gene Set From Biocarta Pathways proteins participating in the induction of apoptosis through dr3 and dr4/5 death receptors pathway from the Biocarta Pathways dataset.
CIITA-18437201-Raji B cells and iDC-human Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CIITA-18437201-Raji B cells and iDC-human transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
VDR-23401126-LCL-AND-THP1-HUMAN Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the VDR-23401126-LCL-AND-THP1-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
BACH1-22875853-HELA-AND-SCP4-HUMAN Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the BACH1-22875853-HELA-AND-SCP4-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
Hypothyroidism, central, and testicular enlargement Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypothyroidism, central, and testicular enlargement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Trifunctional protein deficiency with myopathy and neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Trifunctional protein deficiency with myopathy and neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Foveal hypoplasia and presenile cataract syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arthrogryposis, mental retardation, and seizures Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, mental retardation, and seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Vater association with macrocephaly and ventriculomegaly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Vater association with macrocephaly and ventriculomegaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal hamartomas nephroblastomatosis and fetal gigantism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal hamartomas nephroblastomatosis and fetal gigantism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, lactic acidosis, and sideroblastic anemia 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microtia, hearing impairment, and cleft palate Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microtia, hearing impairment, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ichthyosis, spastic quadriplegia, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ichthyosis, spastic quadriplegia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypermanganesemia with dystonia, polycythemia and cirrhosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypermanganesemia with dystonia, polycythemia and cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined cellular and humoral immune defects with granulomas Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined cellular and humoral immune defects with granulomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined d-2- and l-2-hydroxyglutaric aciduria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined d-2- and l-2-hydroxyglutaric aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sinoatrial node dysfunction and deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sinoatrial node dysfunction and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation with language impairment and autistic features Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation with language impairment and autistic features phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Warts, hypogammaglobulinemia, infections, and myelokathexis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Warts, hypogammaglobulinemia, infections, and myelokathexis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fibular hypoplasia and complex brachydactyly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fibular hypoplasia and complex brachydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation, anterior maxillary protrusion, and strabismus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, anterior maxillary protrusion, and strabismus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile convulsions and paroxysmal choreoathetosis, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile convulsions and paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Insulin-resistant diabetes mellitus AND acanthosis nigricans Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Insulin-resistant diabetes mellitus AND acanthosis nigricans phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Craniofacial anomalies and anterior segment dysgenesis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniofacial anomalies and anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness with labyrinthine aplasia microtia and microdontia (LAMM) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness with labyrinthine aplasia microtia and microdontia (LAMM) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple Cutaneous and Mucosal Venous Malformations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple Cutaneous and Mucosal Venous Malformations 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.
Microcephaly with mental retardation and digital anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly with mental retardation and digital anomalies 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.
Peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Growth retardation, developmental delay, coarse facies, and early death Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Growth retardation, developmental delay, coarse facies, and early death phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inflammatory skin and bowel disease, neonatal, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Anemia sideroblastic and spinocerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Anemia sideroblastic and spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Facial dysmorphism, immunodeficiency, livedo, and short stature Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Facial dysmorphism, immunodeficiency, livedo, and short stature phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, congenital heart defects, and posterior embryotoxon Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infertility associated with multi-tailed spermatozoa and excessive DNA Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infertility associated with multi-tailed spermatozoa and excessive DNA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Iris coloboma with ptosis, hypertelorism, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Iris coloboma with ptosis, hypertelorism, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rigidity and multifocal seizure syndrome, lethal neonatal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rigidity and multifocal seizure syndrome, lethal neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Harmonizome 3.0

Riboflavin and CoQ disorders Gene Set

cocaine-related disorders; opioid-related disorders; substance-related disorders Gene Set

fatigue; sleep disorders; sleep initiation and maintenance disorders Gene Set

alcohol-related disorders; cocaine-related disorders; Gene Set

speech disorders; substance-related disorders Gene Set

alcoholism; opioid-related disorders; substance-related disorders Gene Set

alcoholism; cocaine-related disorders; heroin dependence; substance-related disorders Gene Set

blood coagulation disorders; puerperal disorders; sinus thrombosis, intracranial Gene Set

hearing loss, sensorineural; learning disorders; melas syndrome; migraine disorders; mitochondrial diseases; sensorineural hearing loss Gene Set

craniofacial abnormalities; growth disorders; learning disorders; syndrome Gene Set

articulation disorders; disorders Gene Set

articulation disorders; dyslexia, acquired; language disorders; noonan syndrome; turner's phenotype, karyotype normal Gene Set

alzheimer disease; alzheimer's disease; disorders of excessive somnolence; memory disorders Gene Set

blood coagulation disorders; blood coagulation disorders, inherited; recurrence; thromboembolism; thrombophilia; venous thrombosis Gene Set

personality disorders; eating disorders Gene Set

learning disorders; memory disorders; mental retardation Gene Set

migraine disorders; substance-related disorders Gene Set

cystic fibrosis; growth disorders; nutrition disorders Gene Set

brain injuries; cerebrovascular disorders; migraine disorders Gene Set

apnea; apoplexy; blood coagulation disorders; brain ischemia; cerebrovascular disorders; hypotony, muscle; muscle hypotonia; protein c deficiency; seizures; stroke; thrombosis Gene Set

riboflavin-6822 Gene Set

riboflavin-2760 Gene Set

riboflavin-1767 Gene Set

riboflavin-4485 Gene Set

Riboflavin Gene Set

Riboflavin Monophosphate Gene Set

Riboflavin Gene Set

folic acid deficiency; fractures, bone; osteoporosis, postmenopausal; riboflavin deficiency Gene Set

riboflavin Gene Set

riboflavin transport Gene Set

riboflavin metabolic process Gene Set

riboflavin biosynthetic process Gene Set

riboflavin reductase (nadph) activity Gene Set

riboflavin kinase activity Gene Set

riboflavin transporter activity Gene Set

Riboflavin Gene Set

Riboflavin reduced Gene Set

Riboflavin synthase-like beta-barrel Gene Set

Riboflavin kinase domain Gene Set

Riboflavin kinase Gene Set

Riboflavin kinase domain, bacterial/eukaryotic Gene Set

riboflavin metabolism Gene Set

riboflavin deficiency Gene Set

Vitamin B2 (riboflavin) metabolism Gene Set

Riboflavin Deficiency Gene Set

riboflavin metabolic process Gene Set

riboflavin biosynthetic process Gene Set

riboflavin transport Gene Set

riboflavin reductase (NADPH) activity Gene Set

riboflavin kinase activity Gene Set

riboflavin transmembrane transporter activity Gene Set

Riboflavin Gene Set

Vitamin B2 (riboflavin) metabolism Gene Set

riboflavin metabolic process Gene Set

riboflavin biosynthetic process Gene Set

riboflavin transport Gene Set

riboflavin reductase (NADPH) activity Gene Set

riboflavin kinase activity Gene Set

riboflavin transmembrane transporter activity Gene Set

riboflavin binding Gene Set

Riboflavin deficiency Gene Set

Riboflavin synthase complex Gene Set

Maternal riboflavin deficiency Gene Set

Riboflavin metabolism Gene Set

RIBOFLAVIN Gene Set

Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Set

Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene Set

Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene Set

Epilepsy, X-linked, with variable learning disabilities and behavior disorders Gene Set

Schizophrenia and Disorders with Psychotic Features Gene Set

Sleep Initiation and Maintenance Disorders Gene Set

Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders Gene Set

Attention Deficit and Disruptive Behavior Disorders Gene Set

Attention Deficit and Disruptive Behavior Disorders Gene Set

attention deficit and disruptive behavior disorders Gene Set

alcohol-related disorders; carcinoma, squamous cell; head and neck neoplasms; squamous cell carcinoma; tobacco use disorder Gene Set

fatigue; sleep initiation and maintenance disorders Gene Set

sleep initiation and maintenance disorders Gene Set

insulin; obesity; blood pressure, arterial; blood and blood forming organ disorders Gene Set