atrophy; prenatal exposure delayed effects; substance-related disorders

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Results for "atrophy; prenatal exposure delayed effects; substance-related disorders": 1001 gene sets

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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.
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.
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.
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.
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.
Prenatal Exposure Delayed Effects Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Prenatal Exposure Delayed Effects from the curated CTD Gene-Disease Associations dataset.
asthma; prenatal exposure delayed effects; respiratory sounds Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; prenatal exposure delayed effects; respiratory sounds in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pregnancy complications; prenatal exposure delayed effects; serotonin syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease pregnancy complications; prenatal exposure delayed effects; serotonin syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
prenatal exposure delayed effects; respiratory tract diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease prenatal exposure delayed effects; respiratory tract diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
inflammation; prenatal exposure delayed effects; recurrence; respiratory sounds Gene Set From GAD Gene-Disease Associations genes associated with the disease inflammation; prenatal exposure delayed effects; recurrence; respiratory sounds in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia; prenatal exposure delayed effects Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; prenatal exposure delayed effects Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, drug-induced; epilepsy; prenatal exposure delayed effects Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, drug-induced; epilepsy; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; prenatal exposure delayed effects Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lead poisoning; prenatal exposure delayed effects Gene Set From GAD Gene-Disease Associations genes associated with the disease lead poisoning; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dermatitis, atopic; eczema allergic; prenatal exposure delayed effects Gene Set From GAD Gene-Disease Associations genes associated with the disease dermatitis, atopic; eczema allergic; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft palate; prenatal exposure delayed effects Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft palate; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hiv infections; prenatal exposure delayed effects Gene Set From GAD Gene-Disease Associations genes associated with the disease hiv infections; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pregnancy complications; prenatal exposure delayed effects Gene Set From GAD Gene-Disease Associations genes associated with the disease pregnancy complications; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip; cleft palate; prenatal exposure delayed effects Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip; cleft palate; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia, lymphocytic, acute, l1; precursor cell lymphoblastic leukemia-lymphoma; prenatal exposure delayed effects Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, lymphocytic, acute, l1; precursor cell lymphoblastic leukemia-lymphoma; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; cerebral palsy; intracranial thrombosis; obstetric labor complications; prenatal exposure delayed effects Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; cerebral palsy; intracranial thrombosis; obstetric labor complications; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart defects, congenital; hyperhomocysteinemia; prenatal exposure delayed effects Gene Set From GAD Gene-Disease Associations genes associated with the disease heart defects, congenital; hyperhomocysteinemia; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; prenatal exposure delayed effects; respiratory hypersensitivity; respiratory sounds Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; prenatal exposure delayed effects; respiratory hypersensitivity; respiratory sounds in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
prenatal exposure delayed effects; starvation Gene Set From GAD Gene-Disease Associations genes associated with the disease prenatal exposure delayed effects; starvation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute lymphocytic leukemia; precursor cell lymphoblastic leukemia-lymphoma; prenatal exposure delayed effects Gene Set From GAD Gene-Disease Associations genes associated with the disease acute lymphocytic leukemia; precursor cell lymphoblastic leukemia-lymphoma; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; fetal growth retardation; prenatal exposure delayed effects Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; fetal growth retardation; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
prenatal exposure delayed effects Gene Set From GAD Gene-Disease Associations genes associated with the disease prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Prenatal Exposure Delayed Effects Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Prenatal Exposure Delayed Effects phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Prenatal Exposure Delayed Effects Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Prenatal Exposure Delayed Effects in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
prenatal environment exposure Gene Set From GAD Gene-Disease Associations genes associated with the disease prenatal environment exposure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Prenatal Alcohol Exposure Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Prenatal Alcohol Exposure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neurobehavioral disorder with prenatal alcohol exposure Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurobehavioral disorder with prenatal alcohol exposure in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Motor development (prenatal lead exposure interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Motor development (prenatal lead exposure interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Mental development (prenatal lead exposure interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mental development (prenatal lead exposure interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 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.
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.
muscular atrophy, spinal; spinal muscular atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular atrophy, spinal; spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic atrophy, autosomal dominant; optic atrophy, hereditary, leber Gene Set From GAD Gene-Disease Associations genes associated with the disease optic atrophy, autosomal dominant; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic atrophies, hereditary; optic atrophy, autosomal dominant; optic atrophy, hereditary, leber Gene Set From GAD Gene-Disease Associations genes associated with the disease optic atrophies, hereditary; optic atrophy, autosomal dominant; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 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.
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.
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.
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.
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.
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; 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.
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.
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.
Prenatal Injuries Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Prenatal Injuries from the curated CTD Gene-Disease Associations dataset.
prenatal viability Gene Set From GAD Gene-Disease Associations genes associated with the disease prenatal viability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
breast cancer risk and prenatal viability Gene Set From GAD Gene-Disease Associations genes associated with the disease breast cancer risk and prenatal viability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
prenatal Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term prenatal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
abnormality of prenatal development or birth Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of prenatal development or birth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
prenatal maternal abnormality Gene Set From GWASdb SNP-Phenotype Associations genes associated with the prenatal maternal abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of prenatal development or birth Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of prenatal development or birth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple prenatal fractures Gene Set From HPO Gene-Disease Associations genes associated with the multiple prenatal fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
prenatal maternal abnormality Gene Set From HPO Gene-Disease Associations genes associated with the prenatal maternal abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
prenatal movement abnormality Gene Set From HPO Gene-Disease Associations genes associated with the prenatal movement abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal prenatal growth/weight/body size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal prenatal growth/weight/body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
partial prenatal lethality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the partial prenatal lethality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
prenatal growth retardation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the prenatal growth retardation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
complete prenatal lethality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the complete prenatal lethality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal prenatal body size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal prenatal body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
prenatal lethality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the prenatal lethality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Prenatal Maternal Abnormality Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Prenatal Maternal Abnormality in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of Prenatal Development Or Birth Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Prenatal Development Or Birth in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Prenatal Fractures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Prenatal Fractures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Prenatal Movement Abnormality Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Prenatal Movement Abnormality in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
prenatal lethality, incomplete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the prenatal lethality, incomplete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
prenatal lethality, complete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the prenatal lethality, complete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
prenatal lethality Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the prenatal lethality phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent prenatal movement Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent prenatal movement phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal prenatal growth/weight/body size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal prenatal growth/weight/body size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
prenatal growth retardation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the prenatal growth retardation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
prenatal lethality prior to heart atrial septation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the prenatal lethality prior to heart atrial septation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal prenatal movement Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal prenatal movement phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal prenatal body size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal prenatal body size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
prenatal lethality Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the prenatal lethality phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
prenatal lethality prior to heart atrial septation Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the prenatal lethality prior to heart atrial septation phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
Abnormality of prenatal development or birth Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormality of prenatal development or birth phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Prenatal LIG4 syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Prenatal LIG4 syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Prenatal anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Prenatal anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
H2AX complex, isolated from cells without IR exposure Gene Set From CORUM Protein Complexes proteins in the H2AX complex, isolated from cells without IR exposure protein complex from the CORUM Protein Complexes dataset.
exposure keratitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease exposure keratitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
low mpa exposure and acute rejection in mmf/tacrolimus-treated kidney transplant patients Gene Set From GAD Gene-Disease Associations genes associated with the disease low mpa exposure and acute rejection in mmf/tacrolimus-treated kidney transplant patients in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
exposure to 1,3-butadiene Gene Set From GAD Gene-Disease Associations genes associated with the disease exposure to 1,3-butadiene in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arsnic exposure Gene Set From GAD Gene-Disease Associations genes associated with the disease arsnic exposure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pesticide exposure ; vaccination response Gene Set From GAD Gene-Disease Associations genes associated with the disease pesticide exposure ; vaccination response in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
black carbon exposure Gene Set From GAD Gene-Disease Associations genes associated with the disease black carbon exposure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood brain tumors ; residential insecticide exposure Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood brain tumors ; residential insecticide exposure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dna damage associated with exposure to air pollution Gene Set From GAD Gene-Disease Associations genes associated with the disease dna damage associated with exposure to air pollution in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
high exposure to aflatoxin b1. Gene Set From GAD Gene-Disease Associations genes associated with the disease high exposure to aflatoxin b1. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vinyl chloride monomer-exposure Gene Set From GAD Gene-Disease Associations genes associated with the disease vinyl chloride monomer-exposure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
occupational exposure in lumbar disc degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease occupational exposure in lumbar disc degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
low-level lead exposure Gene Set From GAD Gene-Disease Associations genes associated with the disease low-level lead exposure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vinyl chloride exposure Gene Set From GAD Gene-Disease Associations genes associated with the disease vinyl chloride exposure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
exposure Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term exposure in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
phosphatidylserine exposure on apoptotic cell surface Gene Set From GO Biological Process Annotations 2015 genes participating in the phosphatidylserine exposure on apoptotic cell surface biological process from the curated GO Biological Process Annotations 2015 dataset.
phosphatidylserine exposure on blood platelet Gene Set From GO Biological Process Annotations 2015 genes participating in the phosphatidylserine exposure on blood platelet biological process from the curated GO Biological Process Annotations 2015 dataset.
Lung cancer-asbestos exposure interaction Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Lung cancer-asbestos exposure interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
exposure Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term exposure in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
Exposure Keratoconjunctivitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Exposure Keratoconjunctivitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pulmonary Fibrosis - From Asbestos Exposure Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Fibrosis - From Asbestos Exposure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dental Pulp Exposure Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dental Pulp Exposure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Maternal Teratogenic Exposure Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Maternal Teratogenic Exposure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
positive regulation of phosphatidylserine exposure on apoptotic cell surface Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of phosphatidylserine exposure on apoptotic cell surface biological process from the curated GO Biological Process Annotations 2023 dataset.
phosphatidylserine exposure on blood platelet Gene Set From GO Biological Process Annotations 2023 genes participating in the phosphatidylserine exposure on blood platelet biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of phosphatidylserine exposure on apoptotic cell surface Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of phosphatidylserine exposure on apoptotic cell surface biological process from the curated GO Biological Process Annotations 2023 dataset.
Acrylamide biotransformation and exposure biomarkers Gene Set From WikiPathways Pathways 2024 proteins participating in the Acrylamide biotransformation and exposure biomarkers pathway from the WikiPathways Pathways 2024 dataset.
positive regulation of phosphatidylserine exposure on apoptotic cell surface Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of phosphatidylserine exposure on apoptotic cell surface biological process from the curated GO Biological Process Annotations 2025 dataset.
phosphatidylserine exposure on blood platelet Gene Set From GO Biological Process Annotations 2025 genes participating in the phosphatidylserine exposure on blood platelet biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of phosphatidylserine exposure on apoptotic cell surface Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of phosphatidylserine exposure on apoptotic cell surface biological process from the curated GO Biological Process Annotations 2025 dataset.
Exposure keratitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Exposure keratitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Opioid exposure Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Opioid exposure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hearing loss in noise exposure Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hearing loss in noise exposure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Pneumoconiosis in silica exposure Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pneumoconiosis in silica exposure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Depressive symptoms (SSRI exposure interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Depressive symptoms (SSRI exposure interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Psychological resilience (outcome-based) in high deployment stress exposure Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Psychological resilience (outcome-based) in high deployment stress exposure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Colorectal cancer x fine particulate matter exposure levels interaction Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Colorectal cancer x fine particulate matter exposure levels interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma (time to childhood onset) in early life tobacco smoke exposure Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma (time to childhood onset) in early life tobacco smoke exposure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Lung cancer (asbestos exposure interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lung cancer (asbestos exposure interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Parkinson's disease (pesticide exposure interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parkinson's disease (pesticide exposure interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Esophageal adenocarcinoma x pack-years of smoking exposure interaction Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Esophageal adenocarcinoma x pack-years of smoking exposure interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Barrett's esophagus x pack-years of smoking exposure interaction Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Barrett's esophagus x pack-years of smoking exposure interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Coronary atherosclerosis (increased number of diseased vessels) (traffic exposure interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Coronary atherosclerosis (increased number of diseased vessels) (traffic exposure interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chromosomal aberration frequency (chromosome type) in genotoxic compound exposure Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chromosomal aberration frequency (chromosome type) in genotoxic compound exposure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
High chromosomal aberration frequency (chromatid type) in genotoxic compound exposure Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the High chromosomal aberration frequency (chromatid type) in genotoxic compound exposure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chromosomal aberration frequency (chromatid type) in genotoxic compound exposure Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chromosomal aberration frequency (chromatid type) in genotoxic compound exposure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
High chromosomal aberration frequency (chromosome type) in genotoxic compound exposure Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the High chromosomal aberration frequency (chromosome type) in genotoxic compound exposure 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.
effects of calcineurin in keratinocyte differentiation Gene Set From Biocarta Pathways proteins participating in the effects of calcineurin in keratinocyte differentiation pathway from the Biocarta Pathways dataset.
estramustine phospate side-effects Gene Set From GAD Gene-Disease Associations genes associated with the disease estramustine phospate side-effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sulfasalazine, adverse effects of Gene Set From GAD Gene-Disease Associations genes associated with the disease sulfasalazine, adverse effects of in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
loperamide disposition and central nervous system effects. Gene Set From GAD Gene-Disease Associations genes associated with the disease loperamide disposition and central nervous system effects. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
extrapyramidal side effects Gene Set From GAD Gene-Disease Associations genes associated with the disease extrapyramidal side effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
severe acute radiotherapy side effects Gene Set From GAD Gene-Disease Associations genes associated with the disease severe acute radiotherapy side effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
side-effects of clozapine Gene Set From GAD Gene-Disease Associations genes associated with the disease side-effects of clozapine in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diet effects Gene Set From GAD Gene-Disease Associations genes associated with the disease diet effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcohol effects Gene Set From GAD Gene-Disease Associations genes associated with the disease alcohol effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
antidepressant adverse effects Gene Set From GAD Gene-Disease Associations genes associated with the disease antidepressant adverse effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
citalopram/adverse effects* Gene Set From GAD Gene-Disease Associations genes associated with the disease citalopram/adverse effects* in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
smoking genotoxic effects Gene Set From GAD Gene-Disease Associations genes associated with the disease smoking genotoxic effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
response to antipsychotic therapy (extrapyramidal side effects) Gene Set From GAD Gene-Disease Associations genes associated with the disease response to antipsychotic therapy (extrapyramidal side effects) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
effects Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term effects in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Response to antipsychotic therapy (extrapyramidal side effects) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Response to antipsychotic therapy (extrapyramidal side effects) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Thiazide-induced adverse metabolic effects in hypertensive patients Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Thiazide-induced adverse metabolic effects in hypertensive patients phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
radiation-effects Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term radiation-effects in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
Effects of Botulinum toxin Gene Set From PID Pathways proteins participating in the Effects of Botulinum toxin pathway from the PID Pathways dataset.
Effects of PIP2 hydrolysis Gene Set From Reactome Pathways 2014 proteins participating in the Effects of PIP2 hydrolysis pathway from the Reactome Pathways dataset.
cGMP effects Gene Set From Reactome Pathways 2014 proteins participating in the cGMP effects pathway from the Reactome Pathways dataset.
Insulin effects increased synthesis of Xylulose-5-Phosphate Gene Set From Reactome Pathways 2014 proteins participating in the Insulin effects increased synthesis of Xylulose-5-Phosphate pathway from the Reactome Pathways dataset.
NS1 Mediated Effects on Host Pathways Gene Set From Reactome Pathways 2014 proteins participating in the NS1 Mediated Effects on Host Pathways pathway from the Reactome Pathways dataset.
Effects of Nitric Oxide(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Effects of Nitric Oxide(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Adverse Effects, Not Elsewhere Classified Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adverse Effects, Not Elsewhere Classified in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Effects Of Heat Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Effects Of Heat in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Effects of nitric oxide Gene Set From WikiPathways Pathways 2024 proteins participating in the Effects of nitric oxide pathway from the WikiPathways Pathways 2024 dataset.
Alzheimer 39 s disease and miRNA effects Gene Set From WikiPathways Pathways 2024 proteins participating in the Alzheimer 39 s disease and miRNA effects pathway from the WikiPathways Pathways 2024 dataset.
Overview of nanoparticle effects Gene Set From WikiPathways Pathways 2024 proteins participating in the Overview of nanoparticle effects pathway from the WikiPathways Pathways 2024 dataset.
EV release from cardiac cells and their functional effects Gene Set From WikiPathways Pathways 2024 proteins participating in the EV release from cardiac cells and their functional effects pathway from the WikiPathways Pathways 2024 dataset.
Melatonin metabolism and effects Gene Set From WikiPathways Pathways 2024 proteins participating in the Melatonin metabolism and effects pathway from the WikiPathways Pathways 2024 dataset.
Ethanol effects on histone modifications Gene Set From WikiPathways Pathways 2024 proteins participating in the Ethanol effects on histone modifications pathway from the WikiPathways Pathways 2024 dataset.
Thyroid hormones production and peripheral downstream signaling effects Gene Set From WikiPathways Pathways 2024 proteins participating in the Thyroid hormones production and peripheral downstream signaling effects pathway from the WikiPathways Pathways 2024 dataset.
Antiviral and anti inflammatory effects of Nrf2 on SARS CoV 2 pathway Gene Set From WikiPathways Pathways 2024 proteins participating in the Antiviral and anti inflammatory effects of Nrf2 on SARS CoV 2 pathway pathway from the WikiPathways Pathways 2024 dataset.
Abnormal calcium handling and its effects on muscle contraction in DMD Gene Set From WikiPathways Pathways 2024 proteins participating in the Abnormal calcium handling and its effects on muscle contraction in DMD pathway from the WikiPathways Pathways 2024 dataset.
Effects of MFN2 mutation Gene Set From WikiPathways Pathways 2024 proteins participating in the Effects of MFN2 mutation pathway from the WikiPathways Pathways 2024 dataset.
Effects of PIP2 hydrolysis Gene Set From Reactome Pathways 2024 proteins participating in the Effects of PIP2 hydrolysis pathway from the Reactome Pathways 2024 dataset.
Insulin effects increased synthesis of Xylulose-5-Phosphate Gene Set From Reactome Pathways 2024 proteins participating in the Insulin effects increased synthesis of Xylulose-5-Phosphate pathway from the Reactome Pathways 2024 dataset.
NS1 Mediated Effects on Host Pathways Gene Set From Reactome Pathways 2024 proteins participating in the NS1 Mediated Effects on Host Pathways pathway from the Reactome Pathways 2024 dataset.
SARS-CoV-1-mediated effects on programmed cell death Gene Set From Reactome Pathways 2024 proteins participating in the SARS-CoV-1-mediated effects on programmed cell death pathway from the Reactome Pathways 2024 dataset.
cGMP effects Gene Set From Reactome Pathways 2024 proteins participating in the cGMP effects pathway from the Reactome Pathways 2024 dataset.
Spherical equivalent (joint analysis main effects and education interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Spherical equivalent (joint analysis main effects and education interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to antipsychotic therapy (extrapyramidal side effects) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to antipsychotic therapy (extrapyramidal side effects) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Thiazide-induced adverse metabolic effects in hypertensive patients Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Thiazide-induced adverse metabolic effects in hypertensive patients phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist circumference adjusted for BMI (joint analysis main effects and smoking interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist circumference adjusted for BMI (joint analysis main effects and smoking interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-to-hip ratio adjusted for BMI (joint analysis main effects and smoking interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip ratio adjusted for BMI (joint analysis main effects and smoking interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist circumference adjusted for BMI (joint analysis main effects and physical activity interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist circumference adjusted for BMI (joint analysis main effects and physical activity interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Conotruncal heart defects (maternal effects) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Conotruncal heart defects (maternal effects) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Conotruncal heart defects (inherited effects) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Conotruncal heart defects (inherited effects) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Body mass index (joint analysis main effects and physical activity interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (joint analysis main effects and physical activity interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Body mass index (joint analysis main effects and smoking interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (joint analysis main effects and smoking interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Food allergy (maternal genetic effects) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Food allergy (maternal genetic effects) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Peanut allergy (maternal genetic effects) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Peanut allergy (maternal genetic effects) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Milk allergy (maternal genetic effects) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Milk allergy (maternal genetic effects) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Egg allergy (maternal genetic effects) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Egg allergy (maternal genetic effects) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to ketamine in bipolar disorder or major depression (antidepressant effects) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to ketamine in bipolar disorder or major depression (antidepressant effects) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to ketamine in bipolar disorder or major depression (dissociation effects) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to ketamine in bipolar disorder or major depression (dissociation effects) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
central gray substance of midbrain, right Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in central gray substance of midbrain, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
central glial substance Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in central glial substance relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
central gray substance of midbrain, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in central gray substance of midbrain, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
periaqueductal gray substance, ventral portion Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in periaqueductal gray substance, ventral portion relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
periaqueductal gray substance, dorsolateral portion Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in periaqueductal gray substance, dorsolateral portion relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
lipid mobilizing substance Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical lipid mobilizing substance from the curated CTD Gene-Chemical Interactions dataset.
substance P-saporin Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical substance P-saporin from the curated CTD Gene-Chemical Interactions dataset.
substance P (6-11), Tyr(6)-D-Phe(7)-D-His(9)- Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical substance P (6-11), Tyr(6)-D-Phe(7)-D-His(9)- from the curated CTD Gene-Chemical Interactions dataset.
Psychoses, Substance-Induced Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Psychoses, Substance-Induced from the curated CTD Gene-Disease Associations dataset.
Substance Withdrawal Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Substance Withdrawal Syndrome from the curated CTD Gene-Disease Associations dataset.
substance-induced psychosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease substance-induced psychosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
substance dependence Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease substance dependence in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
substance abuse Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease substance abuse in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
substance P Gene Set From DrugBank Drug Targets interacting proteins for the substance P drug from the curated DrugBank Drug Targets dataset.
antisocial substance dependence. Gene Set From GAD Gene-Disease Associations genes associated with the disease antisocial substance dependence. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
flushing; substance withdrawal syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease flushing; substance withdrawal syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
early onset alcoholism/substance abuse. Gene Set From GAD Gene-Disease Associations genes associated with the disease early onset alcoholism/substance abuse. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
substance dependence Gene Set From GAD Gene-Disease Associations genes associated with the disease substance dependence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
substance abuse Gene Set From GAD Gene-Disease Associations genes associated with the disease substance abuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hepatitis c; hepatitis c, chronic; substance abuse, intravenous; viremia Gene Set From GAD Gene-Disease Associations genes associated with the disease hepatitis c; hepatitis c, chronic; substance abuse, intravenous; viremia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hepatitis c; hepatitis c, chronic; substance abuse, intravenous Gene Set From GAD Gene-Disease Associations genes associated with the disease hepatitis c; hepatitis c, chronic; substance abuse, intravenous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemophilia a; hepatitis c, chronic; substance abuse, intravenous Gene Set From GAD Gene-Disease Associations genes associated with the disease hemophilia a; hepatitis c, chronic; substance abuse, intravenous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild and severe substance abuse Gene Set From GAD Gene-Disease Associations genes associated with the disease mild and severe substance abuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
marijuana abuse; psychoses, substance-induced Gene Set From GAD Gene-Disease Associations genes associated with the disease marijuana abuse; psychoses, substance-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
substance use Gene Set From GAD Gene-Disease Associations genes associated with the disease substance use in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hiv infections; substance abuse, intravenous; [x]human immunodeficiency virus disease Gene Set From GAD Gene-Disease Associations genes associated with the disease hiv infections; substance abuse, intravenous; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia; bipolar disorder; suicide; anorexia nervosa; bulimia; substance abuse Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; bipolar disorder; suicide; anorexia nervosa; bulimia; substance abuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
methamphetamine abuse; substance abuse Gene Set From GAD Gene-Disease Associations genes associated with the disease methamphetamine abuse; substance abuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hepatitis c; substance abuse, intravenous Gene Set From GAD Gene-Disease Associations genes associated with the disease hepatitis c; substance abuse, intravenous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acquired immunodeficiency syndrome; substance abuse, intravenous Gene Set From GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; substance abuse, intravenous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy; hyperhomocysteinemia; recurrence; substance withdrawal syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy; hyperhomocysteinemia; recurrence; substance withdrawal syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
substance dependence, antisocial Gene Set From GAD Gene-Disease Associations genes associated with the disease substance dependence, antisocial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recurrence; substance withdrawal syndrome; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease recurrence; substance withdrawal syndrome; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hiv infections; substance abuse, intravenous Gene Set From GAD Gene-Disease Associations genes associated with the disease hiv infections; substance abuse, intravenous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
substance withdrawal syndrome; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease substance withdrawal syndrome; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
marijuana abuse; substance withdrawal syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease marijuana abuse; substance withdrawal syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
substance withdrawal syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease substance withdrawal syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; kidney failure, chronic; substance withdrawal syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; kidney failure, chronic; substance withdrawal syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholism; substance withdrawal syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholism; substance withdrawal syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
psychoses, substance-induced Gene Set From GAD Gene-Disease Associations genes associated with the disease psychoses, substance-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
substance Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term substance in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
response to organic substance Gene Set From GO Biological Process Annotations 2015 genes participating in the response to organic substance biological process from the curated GO Biological Process Annotations 2015 dataset.
organic substance biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the organic substance biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
substance p catabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the substance p catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
organic substance transport Gene Set From GO Biological Process Annotations 2015 genes participating in the organic substance transport biological process from the curated GO Biological Process Annotations 2015 dataset.
organic substance catabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the organic substance catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
cellular response to organic substance Gene Set From GO Biological Process Annotations 2015 genes participating in the cellular response to organic substance biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of transcription from rna polymerase ii promoter in response to arsenic-containing substance Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of transcription from rna polymerase ii promoter in response to arsenic-containing substance biological process from the curated GO Biological Process Annotations 2015 dataset.
cellular response to toxic substance Gene Set From GO Biological Process Annotations 2015 genes participating in the cellular response to toxic substance biological process from the curated GO Biological Process Annotations 2015 dataset.
organic substance metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the organic substance metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
response to inorganic substance Gene Set From GO Biological Process Annotations 2015 genes participating in the response to inorganic substance biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of transcription from rna polymerase ii promoter in response to arsenic-containing substance Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of transcription from rna polymerase ii promoter in response to arsenic-containing substance biological process from the curated GO Biological Process Annotations 2015 dataset.
cellular response to arsenic-containing substance Gene Set From GO Biological Process Annotations 2015 genes participating in the cellular response to arsenic-containing substance biological process from the curated GO Biological Process Annotations 2015 dataset.
response to toxic substance Gene Set From GO Biological Process Annotations 2015 genes participating in the response to toxic substance biological process from the curated GO Biological Process Annotations 2015 dataset.
cellular response to inorganic substance Gene Set From GO Biological Process Annotations 2015 genes participating in the cellular response to inorganic substance biological process from the curated GO Biological Process Annotations 2015 dataset.
response to arsenic-containing substance Gene Set From GO Biological Process Annotations 2015 genes participating in the response to arsenic-containing substance biological process from the curated GO Biological Process Annotations 2015 dataset.
substance p receptor activity Gene Set From GO Molecular Function Annotations 2015 genes performing the substance p receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
toxic substance binding Gene Set From GO Molecular Function Annotations 2015 genes performing the toxic substance binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
substance p receptor binding Gene Set From GO Molecular Function Annotations 2015 genes performing the substance p receptor binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
substance k receptor activity Gene Set From GO Molecular Function Annotations 2015 genes performing the substance k receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
[D-Arg¹ D-Trp^{7 9} Leu¹¹]substance P Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [D-Arg¹ D-Trp^{7 9} Leu¹¹]substance P ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[D-Pro⁴ D-Trp^{7 9 10}]substance P (4-11) Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [D-Pro⁴ D-Trp^{7 9 10}]substance P (4-11) ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
substance P-(4-11) Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the substance P-(4-11) ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
substance P-OMe Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the substance P-OMe ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
[D-Arg¹ D-Phe⁵ D-Trp^{7 9} Leu¹¹]substance P Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [D-Arg¹ D-Phe⁵ D-Trp^{7 9} Leu¹¹]substance P ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
substance P-(6-11) Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the substance P-(6-11) ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
Substance dependence Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Substance dependence phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
substance dependence Gene Set From GWASdb SNP-Disease Associations genes associated with the disease substance dependence in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
substance abuse Gene Set From GWASdb SNP-Disease Associations genes associated with the disease substance abuse in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
substance-induced psychosis Gene Set From GWASdb SNP-Disease Associations genes associated with the disease substance-induced psychosis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
Substance P Gene Set From HMDB Metabolites of Enzymes interacting proteins for the Substance P metabolite from the curated HMDB Metabolites of Enzymes dataset.
Substance Abuse, Intravenous Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Substance Abuse, Intravenous phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Psychoses, Substance-Induced Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Psychoses, Substance-Induced phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Substance Withdrawal Syndrome Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Substance Withdrawal Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
BRD-A56245458_reichstein/C,Aeos substance/C-s_HEPG2_6.0_h_10.0_um Gene Set From LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules* genes differentially expressed following the BRD-A56245458_reichstein/C,Aeos substance/C-*s_HEPG2_6.0_h_10.0_um small molecule perturbation from the LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.
aversion to addictive substance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the aversion to addictive substance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal behavioral response to addictive substance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal behavioral response to addictive substance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
enhanced behavioral response to addictive substance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the enhanced behavioral response to addictive substance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
preference for addictive substance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the preference for addictive substance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
impaired behavioral response to addictive substance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the impaired behavioral response to addictive substance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Substance Abuse Problem Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Substance Abuse Problem in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Substance Withdrawal Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Substance Withdrawal Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Substance Dependence Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Substance Dependence in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Psychoses, Substance-Induced Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Psychoses, Substance-Induced in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hangover From Any Alcohol Or Other Drugs Substance Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hangover From Any Alcohol Or Other Drugs Substance in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
cellular response to arsenic-containing substance Gene Set From GO Biological Process Annotations 2023 genes participating in the cellular response to arsenic-containing substance biological process from the curated GO Biological Process Annotations 2023 dataset.
cellular response to toxic substance Gene Set From GO Biological Process Annotations 2023 genes participating in the cellular response to toxic substance biological process from the curated GO Biological Process Annotations 2023 dataset.
cellular response to organic substance Gene Set From GO Biological Process Annotations 2023 genes participating in the cellular response to organic substance biological process from the curated GO Biological Process Annotations 2023 dataset.
substance P catabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the substance P catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
cellular response to inorganic substance Gene Set From GO Biological Process Annotations 2023 genes participating in the cellular response to inorganic substance biological process from the curated GO Biological Process Annotations 2023 dataset.
organic substance transport Gene Set From GO Biological Process Annotations 2023 genes participating in the organic substance transport biological process from the curated GO Biological Process Annotations 2023 dataset.
substance P receptor activity Gene Set From GO Molecular Function Annotations 2023 genes performing the substance P receptor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
substance K receptor activity Gene Set From GO Molecular Function Annotations 2023 genes performing the substance K receptor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
abnormal behavioral response to addictive substance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal behavioral response to addictive substance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
enhanced behavioral response to addictive substance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the enhanced behavioral response to addictive substance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
impaired behavioral response to addictive substance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the impaired behavioral response to addictive substance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
low preference for an addictive substance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the low preference for an addictive substance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
high preference for an addictive substance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the high preference for an addictive substance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cellular response to arsenic-containing substance Gene Set From GO Biological Process Annotations 2025 genes participating in the cellular response to arsenic-containing substance biological process from the curated GO Biological Process Annotations 2025 dataset.
cellular response to toxic substance Gene Set From GO Biological Process Annotations 2025 genes participating in the cellular response to toxic substance biological process from the curated GO Biological Process Annotations 2025 dataset.
substance P catabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the substance P catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
substance P receptor binding Gene Set From GO Molecular Function Annotations 2025 genes performing the substance P receptor binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
substance K receptor binding Gene Set From GO Molecular Function Annotations 2025 genes performing the substance K receptor binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
substance P receptor activity Gene Set From GO Molecular Function Annotations 2025 genes performing the substance P receptor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
substance K receptor activity Gene Set From GO Molecular Function Annotations 2025 genes performing the substance K receptor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Substance abuse Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Substance abuse from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Substance dependence Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Substance dependence from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Substance dependence Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Substance dependence in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Substance abuse Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Substance abuse in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Substance abuse Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Substance abuse in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Substance dependence Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Substance dependence in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
substance-induced psychosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease substance-induced psychosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
T-substance anomaly Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the T-substance anomaly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Substance dependence Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Substance dependence phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
[D-ARG1,D-PHE5,D-TRP7,9,LEU11]SUBSTANCE P Gene Set From DGIdb Drug Targets 2026 interacting proteins for the [D-ARG1,D-PHE5,D-TRP7,9,LEU11]SUBSTANCE P drug from theDGIdb Drug Targets 2026 dataset.
[D-ARG1,D-TRP7,9,LEU11]SUBSTANCE P Gene Set From DGIdb Drug Targets 2026 interacting proteins for the [D-ARG1,D-TRP7,9,LEU11]SUBSTANCE P drug from theDGIdb Drug Targets 2026 dataset.
[D-PRO4,D-TRP7,9,10]SUBSTANCE P (4-11) Gene Set From DGIdb Drug Targets 2026 interacting proteins for the [D-PRO4,D-TRP7,9,10]SUBSTANCE P (4-11) drug from theDGIdb Drug Targets 2026 dataset.
SUBSTANCE P Gene Set From DGIdb Drug Targets 2026 interacting proteins for the SUBSTANCE P drug from theDGIdb Drug Targets 2026 dataset.
SUBSTANCE P-(4-11) Gene Set From DGIdb Drug Targets 2026 interacting proteins for the SUBSTANCE P-(4-11) drug from theDGIdb Drug Targets 2026 dataset.
SUBSTANCE P-(6-11) Gene Set From DGIdb Drug Targets 2026 interacting proteins for the SUBSTANCE P-(6-11) drug from theDGIdb Drug Targets 2026 dataset.
SUBSTANCE P-OME Gene Set From DGIdb Drug Targets 2026 interacting proteins for the SUBSTANCE P-OME drug from theDGIdb Drug Targets 2026 dataset.
SCID due to ADA deficiency, delayed onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the SCID due to ADA deficiency, delayed onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Delayed puberty Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Delayed puberty phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypersensitivity, Delayed Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypersensitivity, Delayed from the curated CTD Gene-Disease Associations dataset.
Delayed Emergence from Anesthesia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Delayed Emergence from Anesthesia from the curated CTD Gene-Disease Associations dataset.
Puberty, Delayed Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Puberty, Delayed from the curated CTD Gene-Disease Associations dataset.
menarch; natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious Gene Set From GAD Gene-Disease Associations genes associated with the disease menarch; natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
delayed sleep phase syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease delayed sleep phase syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
delayed onset of glycogenosis type ii. Gene Set From GAD Gene-Disease Associations genes associated with the disease delayed onset of glycogenosis type ii. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
delayed renal graft function Gene Set From GAD Gene-Disease Associations genes associated with the disease delayed renal graft function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
delayed graft function; diabetes mellitus Gene Set From GAD Gene-Disease Associations genes associated with the disease delayed graft function; diabetes mellitus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; puberty, delayed Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; puberty, delayed in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
delayed sleep phase syndrome. Gene Set From GAD Gene-Disease Associations genes associated with the disease delayed sleep phase syndrome. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
delayed graft function Gene Set From GAD Gene-Disease Associations genes associated with the disease delayed graft function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
delayed graft function acute rejection episodes and long-term graft dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease delayed graft function acute rejection episodes and long-term graft dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
delayed graft function; inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease delayed graft function; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
puberty, delayed Gene Set From GAD Gene-Disease Associations genes associated with the disease puberty, delayed in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; delayed graft function; kidney diseases; postoperative complications Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; delayed graft function; kidney diseases; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
menarch; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious Gene Set From GAD Gene-Disease Associations genes associated with the disease menarch; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hiv infections; hypersensitivity, delayed; [x]human immunodeficiency virus disease Gene Set From GAD Gene-Disease Associations genes associated with the disease hiv infections; hypersensitivity, delayed; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
delayed Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term delayed in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
regulation of delayed rectifier potassium channel activity Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of delayed rectifier potassium channel activity biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of delayed rectifier potassium channel activity Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of delayed rectifier potassium channel activity biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of delayed rectifier potassium channel activity Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of delayed rectifier potassium channel activity biological process from the curated GO Biological Process Annotations 2015 dataset.
delayed rectifier potassium channel activity Gene Set From GO Molecular Function Annotations 2015 genes performing the delayed rectifier potassium channel activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
delayed eruption of primary teeth Gene Set From GWASdb SNP-Phenotype Associations genes associated with the delayed eruption of primary teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
delayed eruption of permanent teeth Gene Set From GWASdb SNP-Phenotype Associations genes associated with the delayed eruption of permanent teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
delayed eruption of teeth Gene Set From GWASdb SNP-Phenotype Associations genes associated with the delayed eruption of teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
delayed puberty Gene Set From HPO Gene-Disease Associations genes associated with the delayed puberty phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal delayed hypersensitivity skin test Gene Set From HPO Gene-Disease Associations genes associated with the abnormal delayed hypersensitivity skin test phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed tarsal ossification Gene Set From HPO Gene-Disease Associations genes associated with the delayed tarsal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed myelination Gene Set From HPO Gene-Disease Associations genes associated with the delayed myelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed cranial suture closure Gene Set From HPO Gene-Disease Associations genes associated with the delayed cranial suture closure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed speech and language development Gene Set From HPO Gene-Disease Associations genes associated with the delayed speech and language development phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed patellar ossification Gene Set From HPO Gene-Disease Associations genes associated with the delayed patellar ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed femoral head ossification Gene Set From HPO Gene-Disease Associations genes associated with the delayed femoral head ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed gross motor development Gene Set From HPO Gene-Disease Associations genes associated with the delayed gross motor development phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed phalangeal epiphyseal ossification Gene Set From HPO Gene-Disease Associations genes associated with the delayed phalangeal epiphyseal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed ossification of pubic rami Gene Set From HPO Gene-Disease Associations genes associated with the delayed ossification of pubic rami phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed eruption of permanent teeth Gene Set From HPO Gene-Disease Associations genes associated with the delayed eruption of permanent teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed peripheral myelination Gene Set From HPO Gene-Disease Associations genes associated with the delayed peripheral myelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed pubic bone ossification Gene Set From HPO Gene-Disease Associations genes associated with the delayed pubic bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed closure of the anterior fontanelle Gene Set From HPO Gene-Disease Associations genes associated with the delayed closure of the anterior fontanelle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed eruption of teeth Gene Set From HPO Gene-Disease Associations genes associated with the delayed eruption of teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed oxidation of acetaldehyde Gene Set From HPO Gene-Disease Associations genes associated with the delayed oxidation of acetaldehyde phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
reduced delayed hypersensitivity Gene Set From HPO Gene-Disease Associations genes associated with the reduced delayed hypersensitivity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed menarche Gene Set From HPO Gene-Disease Associations genes associated with the delayed menarche phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed ossification of carpal bones Gene Set From HPO Gene-Disease Associations genes associated with the delayed ossification of carpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed calcaneal ossification Gene Set From HPO Gene-Disease Associations genes associated with the delayed calcaneal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed cns myelination Gene Set From HPO Gene-Disease Associations genes associated with the delayed cns myelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed eruption of primary teeth Gene Set From HPO Gene-Disease Associations genes associated with the delayed eruption of primary teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed skeletal maturation Gene Set From HPO Gene-Disease Associations genes associated with the delayed skeletal maturation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed epiphyseal ossification Gene Set From HPO Gene-Disease Associations genes associated with the delayed epiphyseal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Hypersensitivity, Delayed Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hypersensitivity, Delayed phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Delayed Graft Function Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Delayed Graft Function phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Puberty, Delayed Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Puberty, Delayed phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
delayed axon extension Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed axon extension phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed hepatic development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed hepatic development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed heart looping Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed heart looping phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed bone ossification Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed gastrulation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed gastrulation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed dark adaptation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed dark adaptation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed somite formation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed somite formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed eyelid opening Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed eyelid opening phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed brain development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed brain development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed heart development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed heart development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed male fertility Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed male fertility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed embryo turning Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed embryo turning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed sexual maturation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed sexual maturation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed inner ear development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed inner ear development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed embryo implantation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed embryo implantation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed muscle development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed muscle development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed vaginal opening Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed vaginal opening phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed caudal neuropore closure Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed caudal neuropore closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed wound healing Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed wound healing phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed head development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed head development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed skin barrier formation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed skin barrier formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed allantois development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed allantois development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed blastocyst hatching from the zona pellucida Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed blastocyst hatching from the zona pellucida phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed fertilization Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed fertilization phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed kidney development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed kidney development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed tooth eruption Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed tooth eruption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed optic fissure closure Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed optic fissure closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed ear emergence Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed ear emergence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed rostral neuropore closure Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed rostral neuropore closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed eyelid fusion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed eyelid fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed endochondral bone ossification Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed endochondral bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed fertility Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed fertility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed suture closure Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed suture closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed balanopreputial separation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed balanopreputial separation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed limb development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed limb development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed chorioallantoic fusion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed chorioallantoic fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed neural tube closure Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed neural tube closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed hair regrowth Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed hair regrowth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed female fertility Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed female fertility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed circadian phase Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed circadian phase phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed intestine development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed intestine development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed cellular replicative senescence Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed cellular replicative senescence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed estrous cycle Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed estrous cycle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed cns synapse formation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed cns synapse formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed intramembranous bone ossification Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed intramembranous bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed hair appearance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed hair appearance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed parturition Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed parturition phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
{hiv-1 disease, delayed progression of} Gene Set From OMIM Gene-Disease Associations genes associated with the {hiv-1 disease, delayed progression of} phenotype from the curated OMIM Gene-Disease Associations dataset.
{delayed sleep phase syndrome, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {delayed sleep phase syndrome, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{aids, delayed/rapid progression to} Gene Set From OMIM Gene-Disease Associations genes associated with the {aids, delayed/rapid progression to} phenotype from the curated OMIM Gene-Disease Associations dataset.
Delayed Sleep Phase Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Delayed Sleep Phase Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Delayed Cns Myelination Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Delayed Cns Myelination in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Delayed Delivery Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Delayed Delivery in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Delayed Adrenarche Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Delayed Adrenarche in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Delayed Ischaemic Neurological Deficit Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Delayed Ischaemic Neurological Deficit in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Delayed Sleep Phase Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Delayed Sleep Phase in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Delayed Menarche Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Delayed Menarche in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Delayed Dark Adaptation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Delayed Dark Adaptation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Delayed Bone Age Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Bone Age in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Speech And Language Development Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Speech And Language Development in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Puberty Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Puberty in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Eruption Of Permanent Teeth Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Eruption Of Permanent Teeth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Myelination Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Myelination in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Developmentally Delayed Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Developmentally Delayed in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Ability To Walk Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Ability To Walk in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Hypersensitivity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Hypersensitivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Eruption Of Primary Teeth Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Eruption Of Primary Teeth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Fine Motor Development Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Fine Motor Development in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Peripheral Myelination Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Peripheral Myelination in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Proximal Femoral Epiphyseal Ossification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Proximal Femoral Epiphyseal Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Social Development Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Social Development in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Graft Function Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Graft Function in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Ossification Of Carpal Bones Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Ossification Of Carpal Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Emergence From Anesthesia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Emergence From Anesthesia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Reduced Delayed Hypersensitivity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Delayed Hypersensitivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Epiphyseal Ossification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Epiphyseal Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Calcaneal Ossification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Calcaneal Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Pubic Bone Ossification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Pubic Bone Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Sleep Phase Disorder, Susceptibility To Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Sleep Phase Disorder, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Femoral Head Ossification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Femoral Head Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absent Or Delayed Speech Development Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Or Delayed Speech Development in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Onset Bleeding Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Onset Bleeding in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Ossification Of Pubic Rami Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Ossification Of Pubic Rami in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Tarsal Ossification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Tarsal Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Patellar Ossification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Patellar Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Phalangeal Epiphyseal Ossification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Phalangeal Epiphyseal Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Female Puberty Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Female Puberty in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Ability To Sit Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Ability To Sit in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Ability To Stand Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Ability To Stand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Separation Of Umbilical Cord Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Separation Of Umbilical Cord in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Developmental Milestones Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Developmental Milestones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Delayed Hypersensitivity Skin Test Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Delayed Hypersensitivity Skin Test in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
positive regulation of delayed rectifier potassium channel activity Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of delayed rectifier potassium channel activity biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of delayed rectifier potassium channel activity Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of delayed rectifier potassium channel activity biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of delayed rectifier potassium channel activity Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of delayed rectifier potassium channel activity biological process from the curated GO Biological Process Annotations 2023 dataset.
delayed rectifier potassium channel activity Gene Set From GO Molecular Function Annotations 2023 genes performing the delayed rectifier potassium channel activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
delayed cellular replicative senescence Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed cellular replicative senescence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed kidney development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed kidney development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed embryo turning Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed embryo turning phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed heart development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed heart development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed optic fissure closure Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed optic fissure closure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed somite formation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed somite formation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed eyelid fusion Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed eyelid fusion phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed eyelid opening Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed eyelid opening phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed endochondral bone ossification Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed endochondral bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed heart looping Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed heart looping phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed tooth eruption Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed tooth eruption phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed peripheral nervous system regeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed peripheral nervous system regeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed neural tube closure Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed neural tube closure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed bone ossification Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed hepatic development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed hepatic development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed muscle development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed muscle development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed fertility Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed fertility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed hair appearance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed hair appearance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed sexual maturation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed sexual maturation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed intramembranous bone ossification Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed intramembranous bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed wound healing Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed wound healing phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed parturition Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed parturition phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed ear emergence Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed ear emergence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed vaginal opening Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed vaginal opening phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed chorioallantoic fusion Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed chorioallantoic fusion phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed skeletal muscle regeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed skeletal muscle regeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed estrus Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed estrus phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed fertilization Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed fertilization phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed circadian behavior phase Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed circadian behavior phase phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed male fertility Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed male fertility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed brain development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed brain development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed allantois development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed allantois development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed female fertility Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed female fertility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed estrous cycle Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed estrous cycle phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed dark adaptation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed dark adaptation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed inner ear development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed inner ear development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed hair regrowth Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed hair regrowth phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed cranial suture closure Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed cranial suture closure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed intestine development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed intestine development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed axon extension Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed axon extension phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed fontanelle closure Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed fontanelle closure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed CNS synapse formation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed CNS synapse formation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed gastrulation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed gastrulation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed chondrocyte differentiation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed chondrocyte differentiation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed pancreas regeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed pancreas regeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed palatal shelf elevation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed palatal shelf elevation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed embryo implantation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed embryo implantation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed liver regeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed liver regeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed rostral neuropore closure Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed rostral neuropore closure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed limb development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed limb development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed caudal neuropore closure Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed caudal neuropore closure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed blastocyst hatching from the zona pellucida Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed blastocyst hatching from the zona pellucida phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed balanopreputial separation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed balanopreputial separation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed exit from anagen phase Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed exit from anagen phase phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed bone mineralization Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed bone mineralization phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed skin barrier formation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed skin barrier formation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed suckling reflex loss Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed suckling reflex loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed head development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed head development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed reproductive senescence Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed reproductive senescence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed sagittal suture closure Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed sagittal suture closure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed skin pigmentation appearance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed skin pigmentation appearance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed emergence of vibrissae Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed emergence of vibrissae phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
positive regulation of delayed rectifier potassium channel activity Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of delayed rectifier potassium channel activity biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of delayed rectifier potassium channel activity Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of delayed rectifier potassium channel activity biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of delayed rectifier potassium channel activity Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of delayed rectifier potassium channel activity biological process from the curated GO Biological Process Annotations 2025 dataset.
delayed rectifier potassium channel activity Gene Set From GO Molecular Function Annotations 2025 genes performing the delayed rectifier potassium channel activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
hypotonia, ataxia, and delayed development syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease hypotonia, ataxia, and delayed development syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Delayed sleep phase syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Delayed sleep phase syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
organophosphate-induced delayed polyneuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease organophosphate-induced delayed polyneuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Delayed gross motor development Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Delayed gross motor development phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Delayed speech and language development Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Delayed speech and language development phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Delayed puberty Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Delayed puberty phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Reduced delayed hypersensitivity Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Reduced delayed hypersensitivity phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Choanal atresia-athelia-hypothyroidism-delayed puberty-short stature syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Choanal atresia-athelia-hypothyroidism-delayed puberty-short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Absent or delayed speech development Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Absent or delayed speech development phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Delayed fine motor development Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Delayed fine motor development phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Delayed CNS myelination Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Delayed CNS myelination phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Verbal memory performance (residualized delayed recall level) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Verbal memory performance (residualized delayed recall level) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Long-term memory (delayed word recall task) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Long-term memory (delayed word recall task) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Delayed reward discounting Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Delayed reward discounting phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Logical memory (delayed recall) in mild cognitive impairment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Logical memory (delayed recall) in mild cognitive impairment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Logical memory (delayed recall) in Alzheimer's disease dementia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Logical memory (delayed recall) in Alzheimer's disease dementia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Logical memory (delayed recall) in normal cognition Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Logical memory (delayed recall) in normal cognition phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Logical memory (delayed recall) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Logical memory (delayed recall) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Bosch-boonstra-schaaf optic atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bosch-boonstra-schaaf optic atrophy syndrome 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.
Optic atrophy 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Optic atrophy 7 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.
Dominant hereditary optic atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dominant hereditary optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinal muscular atrophy, type II Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distal spinal muscular atrophy, X-linked 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal spinal muscular atrophy, X-linked 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked myopathy with postural muscle atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked myopathy with postural muscle atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Optic atrophy and cataract, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Optic atrophy and cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Optic Atrophy Type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Optic Atrophy Type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinal muscular atrophy, lower extremity predominant 1, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy, lower extremity predominant 1, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary motor and sensory neuropathy with optic atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary motor and sensory neuropathy with optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcornea, myopic chorioretinal atrophy, and telecanthus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcornea, myopic chorioretinal atrophy, and telecanthus 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.
Congenital microvillous atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital microvillous atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, postnatal progressive, with seizures and brain atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, postnatal progressive, with seizures and brain atrophy 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.
Distal spinal muscular atrophy, autosomal recessive 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal spinal muscular atrophy, autosomal recessive 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sveinsson Chorioretinal Atrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sveinsson Chorioretinal Atrophy from the curated CTD Gene-Disease Associations dataset.
Optic Atrophy, Hereditary, Leber Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy, Hereditary, Leber from the curated CTD Gene-Disease Associations dataset.
Spinal muscular atrophy, Jerash type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal muscular atrophy, Jerash type from the curated CTD Gene-Disease Associations dataset.
Optic atrophy 1 and deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy 1 and deafness from the curated CTD Gene-Disease Associations dataset.
Optic Atrophy 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy 7 from the curated CTD Gene-Disease Associations dataset.
Optic Atrophy 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy 4 from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Spinal muscular atrophy 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal muscular atrophy 4 from the curated CTD Gene-Disease Associations dataset.
Optic atrophy 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy 5 from the curated CTD Gene-Disease Associations dataset.
MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY from the curated CTD Gene-Disease Associations dataset.
Spinal muscular atrophy with respiratory distress 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal muscular atrophy with respiratory distress 1 from the curated CTD Gene-Disease Associations dataset.
Atrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrophy from the curated CTD Gene-Disease Associations dataset.
Muscular Atrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Atrophy from the curated CTD Gene-Disease Associations dataset.
Myopathy, X-Linked, With Postural Muscle Atrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, X-Linked, With Postural Muscle Atrophy from the curated CTD Gene-Disease Associations dataset.
Costeff optic atrophy syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Costeff optic atrophy syndrome from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 from the curated CTD Gene-Disease Associations dataset.
Optic atrophy polyneuropathy deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy polyneuropathy deafness from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia, Optic Atrophy, and Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia, Optic Atrophy, and Neuropathy from the curated CTD Gene-Disease Associations dataset.
Chorioretinal atrophy, progressive bifocal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Chorioretinal atrophy, progressive bifocal from the curated CTD Gene-Disease Associations dataset.
Optic atrophy 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy 6 from the curated CTD Gene-Disease Associations dataset.
Optic atrophy and cataract, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy and cataract, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Gyrate Atrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gyrate Atrophy from the curated CTD Gene-Disease Associations dataset.
Optic Atrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy from the curated CTD Gene-Disease Associations dataset.
Pigmented Paravenous Chorioretinal Atrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pigmented Paravenous Chorioretinal Atrophy from the curated CTD Gene-Disease Associations dataset.
OPTIC ATROPHY 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease OPTIC ATROPHY 2 from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Distal, Congenital Nonprogressive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Congenital Nonprogressive from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Distal, X-Linked 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, X-Linked 3 from the curated CTD Gene-Disease Associations dataset.
SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY from the curated CTD Gene-Disease Associations dataset.
Optic Atrophy, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Muscular Atrophy, Spinal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Atrophy, Spinal from the curated CTD Gene-Disease Associations dataset.
spinal muscular atrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease spinal muscular atrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
dentatorubral-pallidoluysian atrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease dentatorubral-pallidoluysian atrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
multiple system atrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease multiple system atrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
adult spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease adult spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
atrophy of prostate Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease atrophy of prostate in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
juvenile spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease juvenile spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
intermediate spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease intermediate spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
primary optic atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary optic atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
skin atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease skin atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
atrophy of testis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease atrophy of testis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple system atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple system atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hereditary choroidal atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary choroidal atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
dentatorubral-pallidoluysian atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dentatorubral-pallidoluysian atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
partial optic atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease partial optic atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
progressive muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease progressive muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
olivopontocerebellar atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease olivopontocerebellar atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
optic atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease optic atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
survival motor neuron spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease survival motor neuron spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
gyrate atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gyrate atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
choroidal neovascularization; geographic atrophy; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; geographic atrophy; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; atrophy; dementia; Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy; dementia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular atrophy; pulmonary disease, chronic obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular atrophy; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; gastritis; helicobacter infections; metaplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; gastritis; helicobacter infections; metaplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroidal neovascularization; geographic atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; geographic atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
posterior cortical atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease posterior cortical atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
geographic atrophy; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease geographic atrophy; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; helicobacter infections; stomach neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; helicobacter infections; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; helicobacter infections Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; helicobacter infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease brain atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic disc atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease optic disc atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease optic atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gyrate atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease gyrate atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
geographic atrophy; macular degeneration; retinal drusen Gene Set From GAD Gene-Disease Associations genes associated with the disease geographic atrophy; macular degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; dementia Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; dementia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; peptic ulcer Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; peptic ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blindness; optic atrophy, hereditary, leber Gene Set From GAD Gene-Disease Associations genes associated with the disease blindness; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; dyspepsia; gastritis; helicobacter infections; peptic ulcer Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; dyspepsia; gastritis; helicobacter infections; peptic ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; gastritis; helicobacter infections; precancerous conditions; stomach neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; gastritis; helicobacter infections; precancerous conditions; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenocarcinoma; atrophy; esophageal neoplasms; gastroesophageal reflux; helicobacter infections; oesophageal neoplasm Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; atrophy; esophageal neoplasms; gastroesophageal reflux; helicobacter infections; oesophageal neoplasm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; atrophy; Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple system atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; brain diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; brain diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; choroidal neovascularization; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; choroidal neovascularization; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; gastritis; inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; gastritis; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular atrophy, spinal Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular atrophy, spinal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; duodenal ulcer; helicobacter infections; peptic ulcer; stomach ulcer; stomach; ulcer Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; duodenal ulcer; helicobacter infections; peptic ulcer; stomach ulcer; stomach; ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; aphasia; atrophy; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; aphasia; atrophy; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; parkinson's disease; multiple system atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease; multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinal muscular atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; dna damage; gastritis, atrophic; metaplasia; stomach neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; dna damage; gastritis, atrophic; metaplasia; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; multiple sclerosis, relapsing-remitting Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; multiple sclerosis, relapsing-remitting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
als/amyotrophic lateral sclerosis; progressive muscular atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease als/amyotrophic lateral sclerosis; progressive muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gastric atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease gastric atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic atrophy, hereditary, leber Gene Set From GAD Gene-Disease Associations genes associated with the disease optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinal muscular atrophy phenotype Gene Set From GAD Gene-Disease Associations genes associated with the disease spinal muscular atrophy phenotype in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; amnesia; atrophy; Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; amnesia; atrophy; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stomach cancer; stomach atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease stomach cancer; stomach atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholism; atrophy; brain diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholism; atrophy; brain diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; epilepsy; hyperhomocysteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; epilepsy; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic atrophy and moderate deafness Gene Set From GAD Gene-Disease Associations genes associated with the disease optic atrophy and moderate deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; atrophy; disease progression Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; gastritis; helicobacter infections; stomach neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; gastritis; helicobacter infections; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia; brain atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; brain atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; huntington disease Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; huntington disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hippocampal atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease hippocampal atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term atrophy in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Spinal Muscular Atrophy, Infantile_CNS - Spinal Cord (MMHCC)_GSE3075 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Spinal Muscular Atrophy, Infantile_CNS - Spinal Cord (MMHCC)_GSE3075 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
skeletal muscle atrophy Gene Set From GO Biological Process Annotations 2015 genes participating in the skeletal muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of muscle atrophy Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of muscle atrophy Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset.
striated muscle atrophy Gene Set From GO Biological Process Annotations 2015 genes participating in the striated muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset.
muscle atrophy Gene Set From GO Biological Process Annotations 2015 genes participating in the muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset.
MRI atrophy measures Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the MRI atrophy measures phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Hippocampal atrophy Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Hippocampal atrophy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
muscular atrophy Gene Set From GWASdb SNP-Disease Associations genes associated with the disease muscular atrophy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
motor neuron atrophy Gene Set From GWASdb SNP-Phenotype Associations genes associated with the motor neuron atrophy phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
atrophy/degeneration affecting the central nervous system Gene Set From GWASdb SNP-Phenotype Associations genes associated with the atrophy/degeneration affecting the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
type 2 muscle fiber atrophy Gene Set From HPO Gene-Disease Associations genes associated with the type 2 muscle fiber atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
levator palpebrae superioris atrophy Gene Set From HPO Gene-Disease Associations genes associated with the levator palpebrae superioris atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral white matter atrophy Gene Set From HPO Gene-Disease Associations genes associated with the cerebral white matter atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy/degeneration affecting the central nervous system Gene Set From HPO Gene-Disease Associations genes associated with the atrophy/degeneration affecting the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar cortical atrophy Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy/degeneration involving the corticospinal tracts Gene Set From HPO Gene-Disease Associations genes associated with the atrophy/degeneration involving the corticospinal tracts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized limb muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the generalized limb muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
global brain atrophy Gene Set From HPO Gene-Disease Associations genes associated with the global brain atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peripheral retinal atrophy Gene Set From HPO Gene-Disease Associations genes associated with the peripheral retinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
caudate atrophy Gene Set From HPO Gene-Disease Associations genes associated with the caudate atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
corpus callosum atrophy Gene Set From HPO Gene-Disease Associations genes associated with the corpus callosum atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
tubular atrophy Gene Set From HPO Gene-Disease Associations genes associated with the tubular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
thenar muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the thenar muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral atrophy Gene Set From HPO Gene-Disease Associations genes associated with the cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pontocerebellar atrophy Gene Set From HPO Gene-Disease Associations genes associated with the pontocerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
diffuse cerebellar atrophy Gene Set From HPO Gene-Disease Associations genes associated with the diffuse cerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
brain atrophy Gene Set From HPO Gene-Disease Associations genes associated with the brain atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
skeletal muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the skeletal muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
tongue atrophy Gene Set From HPO Gene-Disease Associations genes associated with the tongue atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
olivopontocerebellar atrophy Gene Set From HPO Gene-Disease Associations genes associated with the olivopontocerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
optic atrophy Gene Set From HPO Gene-Disease Associations genes associated with the optic atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
dermal atrophy Gene Set From HPO Gene-Disease Associations genes associated with the dermal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peripapillary chorioretinal atrophy Gene Set From HPO Gene-Disease Associations genes associated with the peripapillary chorioretinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
frontal cortical atrophy Gene Set From HPO Gene-Disease Associations genes associated with the frontal cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
subcortical cerebral atrophy Gene Set From HPO Gene-Disease Associations genes associated with the subcortical cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
muscle fiber atrophy Gene Set From HPO Gene-Disease Associations genes associated with the muscle fiber atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
diffuse skin atrophy Gene Set From HPO Gene-Disease Associations genes associated with the diffuse skin atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hand muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the hand muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
motor neuron atrophy Gene Set From HPO Gene-Disease Associations genes associated with the motor neuron atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pelvic girdle muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the pelvic girdle muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive distal muscular atrophy Gene Set From HPO Gene-Disease Associations genes associated with the progressive distal muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar atrophy Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
leber optic atrophy Gene Set From HPO Gene-Disease Associations genes associated with the leber optic atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peripheral axonal atrophy Gene Set From HPO Gene-Disease Associations genes associated with the peripheral axonal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal pigment epithelial atrophy Gene Set From HPO Gene-Disease Associations genes associated with the retinal pigment epithelial atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
fundus atrophy Gene Set From HPO Gene-Disease Associations genes associated with the fundus atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
scapular muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the scapular muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy/degeneration affecting the cerebrum Gene Set From HPO Gene-Disease Associations genes associated with the atrophy/degeneration affecting the cerebrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
first dorsal interossei muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the first dorsal interossei muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
nonprogressive muscular atrophy Gene Set From HPO Gene-Disease Associations genes associated with the nonprogressive muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy/degeneration affecting the brainstem Gene Set From HPO Gene-Disease Associations genes associated with the atrophy/degeneration affecting the brainstem phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy/degeneration involving the caudate nucleus Gene Set From HPO Gene-Disease Associations genes associated with the atrophy/degeneration involving the caudate nucleus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
optic atrophy from cranial nerve compression Gene Set From HPO Gene-Disease Associations genes associated with the optic atrophy from cranial nerve compression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar vermis atrophy Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar vermis atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
villous atrophy Gene Set From HPO Gene-Disease Associations genes associated with the villous atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
iris atrophy Gene Set From HPO Gene-Disease Associations genes associated with the iris atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy of alveolar ridges Gene Set From HPO Gene-Disease Associations genes associated with the atrophy of alveolar ridges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal atrophy Gene Set From HPO Gene-Disease Associations genes associated with the renal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spinal muscular atrophy Gene Set From HPO Gene-Disease Associations genes associated with the spinal muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
interosseus muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the interosseus muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy/degeneration involving the spinal cord Gene Set From HPO Gene-Disease Associations genes associated with the atrophy/degeneration involving the spinal cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
type 1 muscle fiber atrophy Gene Set From HPO Gene-Disease Associations genes associated with the type 1 muscle fiber atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral cortical atrophy Gene Set From HPO Gene-Disease Associations genes associated with the cerebral cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
superior rectus atrophy Gene Set From HPO Gene-Disease Associations genes associated with the superior rectus atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
noninflammatory macular atrophy Gene Set From HPO Gene-Disease Associations genes associated with the noninflammatory macular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized cerebral atrophy/hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the generalized cerebral atrophy/hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
diffuse cerebral atrophy Gene Set From HPO Gene-Disease Associations genes associated with the diffuse cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limb-girdle muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the limb-girdle muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
testicular atrophy Gene Set From HPO Gene-Disease Associations genes associated with the testicular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
shoulder girdle muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the shoulder girdle muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pigmented paravenous chorioretinal atrophy Gene Set From HPO Gene-Disease Associations genes associated with the pigmented paravenous chorioretinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal cortical atrophy Gene Set From HPO Gene-Disease Associations genes associated with the renal cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peroneal muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the peroneal muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy of the spinal cord Gene Set From HPO Gene-Disease Associations genes associated with the atrophy of the spinal cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
chorioretinal atrophy Gene Set From HPO Gene-Disease Associations genes associated with the chorioretinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
frontotemporal cerebral atrophy Gene Set From HPO Gene-Disease Associations genes associated with the frontotemporal cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy of the dentate nucleus Gene Set From HPO Gene-Disease Associations genes associated with the atrophy of the dentate nucleus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
quadriceps muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the quadriceps muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spinocerebellar atrophy Gene Set From HPO Gene-Disease Associations genes associated with the spinocerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal atrophy Gene Set From HPO Gene-Disease Associations genes associated with the retinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
temporal cortical atrophy Gene Set From HPO Gene-Disease Associations genes associated with the temporal cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Atrophy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Multiple System Atrophy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple System Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Optic Atrophy, Hereditary, Leber Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Atrophy, Hereditary, Leber phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Optic Atrophy, Autosomal Dominant Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Atrophy, Autosomal Dominant phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Muscular Atrophy, Spinal Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Atrophy, Spinal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Optic Atrophy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Muscular Atrophy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Geographic Atrophy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Geographic Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Optic atrophy 3-like Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Optic atrophy 3-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.
dentatorubropallidoluysian atrophy Gene Set From KEGG Pathways proteins participating in the dentatorubropallidoluysian atrophy pathway from the KEGG Pathways dataset.
ovary atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ovary atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
skeletal muscle fiber atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the skeletal muscle fiber atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
kidney cortex atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the kidney cortex atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
kidney atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the kidney atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
testicular atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the testicular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
kidney collecting duct atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the kidney collecting duct atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
thymus atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the thymus atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
brain atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the brain atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
skeletal muscle atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the skeletal muscle atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
optic nerve atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the optic nerve atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal pigment epithelium atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal pigment epithelium atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
sebaceous gland atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the sebaceous gland atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
midbrain atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the midbrain atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
renal tubule atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the renal tubule atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
seminal vesicle atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the seminal vesicle atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
renal glomerulus atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the renal glomerulus atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
meibomian gland atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the meibomian gland atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
uterus atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the uterus atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pancreatic acinar cell atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pancreatic acinar cell atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
endometrium atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the endometrium atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
epidermal atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the epidermal atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
exocrine pancreas atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the exocrine pancreas atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
spleen atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the spleen atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
iris atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the iris atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
vagina atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the vagina atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to induced muscular atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased susceptibility to induced muscular atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
vulva atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the vulva atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
muscular atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pancreas atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pancreas atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
oviduct atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the oviduct atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
external male genitalia atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the external male genitalia atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
kidney medulla atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the kidney medulla atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
kidney papillary atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the kidney papillary atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
spinal muscular atrophy, distal, autosomal recessive, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, autosomal recessive, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, distal, autosomal recessive, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, autosomal recessive, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
optic atrophy 6 Gene Set From OMIM Gene-Disease Associations genes associated with the optic atrophy 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
optic atrophy 5 Gene Set From OMIM Gene-Disease Associations genes associated with the optic atrophy 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
optic atrophy 1 Gene Set From OMIM Gene-Disease Associations genes associated with the optic atrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
optic atrophy-4 Gene Set From OMIM Gene-Disease Associations genes associated with the optic atrophy-4 phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, postnatal progressive, with seizures and brain atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy with progressive myoclonic epilepsy Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy with progressive myoclonic epilepsy phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, x-linked 2, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, x-linked 2, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy-2 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-2 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy-3 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-3 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy-1 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-1 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy-4 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-4 phenotype from the curated OMIM Gene-Disease Associations dataset.
{multiple system atrophy, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {multiple system atrophy, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, x-linked, with postural muscle atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, x-linked, with postural muscle atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, chronic distal, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, chronic distal, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, jokela type Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, jokela type phenotype from the curated OMIM Gene-Disease Associations dataset.
sveinsson choreoretinal atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the sveinsson choreoretinal atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
scapuloperoneal spinal muscular atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the scapuloperoneal spinal muscular atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, late-onset, finkel type Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, late-onset, finkel type phenotype from the curated OMIM Gene-Disease Associations dataset.
dentatorubro-pallidoluysian atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the dentatorubro-pallidoluysian atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
{spinal muscular atrophy, type iii, modifier of} Gene Set From OMIM Gene-Disease Associations genes associated with the {spinal muscular atrophy, type iii, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.
optic atrophy-7 Gene Set From OMIM Gene-Disease Associations genes associated with the optic atrophy-7 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, lower extremity-predominant 1, ad Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, lower extremity-predominant 1, ad phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia, optic atrophy, and neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia, optic atrophy, and neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
bosch-boonstra-schaaf optic atrophy syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the bosch-boonstra-schaaf optic atrophy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
optic atrophy 2, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the optic atrophy 2, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
gyrate atrophy of choroid and retina with or without ornithinemia Gene Set From OMIM Gene-Disease Associations genes associated with the gyrate atrophy of choroid and retina with or without ornithinemia phenotype from the curated OMIM Gene-Disease Associations dataset.
optic atrophy 3 with cataract Gene Set From OMIM Gene-Disease Associations genes associated with the optic atrophy 3 with cataract phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, lower extremity-predominant, 2, ad Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, lower extremity-predominant, 2, ad phenotype from the curated OMIM Gene-Disease Associations dataset.
microcornea, myopic chorioretinal atrophy, and telecanthus Gene Set From OMIM Gene-Disease Associations genes associated with the microcornea, myopic chorioretinal atrophy, and telecanthus phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, distal, x-linked 3 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, x-linked 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set From OMIM Gene-Disease Associations genes associated with the short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated OMIM Gene-Disease Associations dataset.
pigmented paravenous chorioretinal atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the pigmented paravenous chorioretinal atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
?neurodegeneration with optic atrophy, childhood onset Gene Set From OMIM Gene-Disease Associations genes associated with the ?neurodegeneration with optic atrophy, childhood onset phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal and bulbar muscular atrophy of kennedy Gene Set From OMIM Gene-Disease Associations genes associated with the spinal and bulbar muscular atrophy of kennedy phenotype from the curated OMIM Gene-Disease Associations dataset.
optic atrophy plus syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the optic atrophy plus syndrome 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.
spinal muscular atrophy, distal, congenital nonprogressive Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, congenital nonprogressive phenotype from the curated OMIM Gene-Disease Associations dataset.
{leber optic atrophy, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {leber optic atrophy, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
Optic Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Optic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Geographic Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Geographic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bulbo-Spinal Atrophy, X-Linked Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bulbo-Spinal Atrophy, X-Linked in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chorioretinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chorioretinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Pigment Epithelium Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Pigment Epithelium Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Cortical Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Linear Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Linear Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Brain Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Brain Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Testis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Testis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Olivopontocerebellar Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Olivopontocerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Infantile Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Infantile Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Limb Muscle Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Limb Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Muscle Fiber Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Muscle Fiber Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple System Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple System Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Motor Neuron Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Motor Neuron Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Subcortical Cerebral Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Subcortical Cerebral Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sveinsson Chorioretinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sveinsson Chorioretinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Kidney Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Kidney in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Villous Atrophy Of Intestine Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Villous Atrophy Of Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Progressive Retinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Progressive Retinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Frontotemporal Cerebral Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Frontotemporal Cerebral Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Cerebral Atrophy/Hypoplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Cerebral Atrophy/Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dentatorubral-Pallidoluysian Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dentatorubral-Pallidoluysian Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy, Disuse Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy, Disuse in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of The Spinal Cord Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of The Spinal Cord in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Corpus Callosum Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Corpus Callosum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral White Matter Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral White Matter Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Prostate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Prostate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pelvic Girdle Muscle Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pelvic Girdle Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Growth Retardation, Alopecia, Pseudoanodontia And Optic Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Growth Retardation, Alopecia, Pseudoanodontia And Optic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Proximal Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Proximal Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy, Muscular, Spinobulbar Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy, Muscular, Spinobulbar in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Proliferative Inflammatory Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Proliferative Inflammatory Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Gyrate Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Gyrate Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Distal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Distal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy/Degeneration Affecting The Brainstem Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy/Degeneration Affecting The Brainstem in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Frontal Cortical Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Frontal Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple System Atrophy, Cerebellar Variant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple System Atrophy, Cerebellar Variant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Temporal Cortical Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Temporal Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Optic Disc Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Optic Disc in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Cortical Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dominant Hereditary Optic Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dominant Hereditary Optic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Retinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Retinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Encephalopathy With Edema, Hypsarrhythmia, And Optic Atrophy-Like Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Encephalopathy With Edema, Hypsarrhythmia, And Optic Atrophy-Like Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Liver Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Liver in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Atrophy Of Ovary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Atrophy Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Pancreas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Tongue Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Tongue in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peroneal Muscular Atrophy (Axonal Type) (Hypertrophic Type) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peroneal Muscular Atrophy (Axonal Type) (Hypertrophic Type) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Paravenous Chorioretinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Paravenous Chorioretinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pigmented Paravenous Chorioretinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pigmented Paravenous Chorioretinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Limb-Girdle Muscle Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Limb-Girdle Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Posterior Cortical Atrophy Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Posterior Cortical Atrophy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Vagina Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Vagina in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Urogenital Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Urogenital Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peroneal Muscle Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peroneal Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Juvenile Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Juvenile Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chorioretinal Atrophy, Progressive Bifocal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chorioretinal Atrophy, Progressive Bifocal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Auditory Neuropathy And Optic Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Auditory Neuropathy And Optic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Diffuse Skin Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Diffuse Skin Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cervical Spinal Cord Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cervical Spinal Cord Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Splenic Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Splenic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Atrophy Of Thyroid Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Atrophy Of Thyroid in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sporadic Olivopontocerebellar Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sporadic Olivopontocerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Axonal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Axonal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Tongue Papillae Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Tongue Papillae in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pancreatic Acinar Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pancreatic Acinar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Retinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Retinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Renal Tubular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Renal Tubular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Renal Cortical Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Renal Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Glaucomatous Atrophy Of Optic Disc Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Glaucomatous Atrophy Of Optic Disc in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Leber Optic Atrophy And Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Leber Optic Atrophy And Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Seminal Vesicle Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Seminal Vesicle in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripapillary Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripapillary Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Gyrate Atrophy Of Choroid And Retina With Pyridoxine-Responsive Ornithinemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Gyrate Atrophy Of Choroid And Retina With Pyridoxine-Responsive Ornithinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Optic Atrophy Plus Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Optic Atrophy Plus Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late Cortical Cerebellar Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late Cortical Cerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rectus Femoris Muscle Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rectus Femoris Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Parietal Cortical Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Parietal Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myelopathic Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myelopathic Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Oculopharyngeal Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Oculopharyngeal Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Proximal Myelopathic Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Proximal Myelopathic Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Scapuloperoneal Form Of Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Scapuloperoneal Form Of Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Cerebral Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Cerebral Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nonprogressive Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nonprogressive Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Periodontal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Periodontal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Skeletal Muscle Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Skeletal Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Foveal Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Foveal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Pigment Epithelial Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Pigment Epithelial Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hippocampal Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hippocampal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Distal Muscle Atrophy Due To Neurologic Disease Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Muscle Atrophy Due To Neurologic Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hand Muscle Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hand Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Shoulder Girdle Muscle Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Shoulder Girdle Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Global Brain Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Global Brain Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Choriocapillaris Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Choriocapillaris Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mucosal Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mucosal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Villous Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Villous Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy/Degeneration Involving The Caudate Nucleus Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy/Degeneration Involving The Caudate Nucleus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy Of Quadriceps Femoris Muscle Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy Of Quadriceps Femoris Muscle in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Muscle Fiber Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscle Fiber Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Muscular Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neurogenic Muscular Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neurogenic Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multiple System Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple System Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Diffuse Cerebral Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Diffuse Cerebral Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy Of The Dentate Nucleus Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy Of The Dentate Nucleus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Corticospinal Tract Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Corticospinal Tract Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Purkinje Layer Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Purkinje Layer Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Vermis Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Vermis Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy/Degeneration Involving The Corticospinal Tracts Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy/Degeneration Involving The Corticospinal Tracts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Extremity Muscle Atrophy, Lower Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Extremity Muscle Atrophy, Lower in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Caudate Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Caudate Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
First Dorsal Interossei Muscle Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype First Dorsal Interossei Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Thenar Muscle Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thenar Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Diffuse Cerebellar Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Diffuse Cerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy Of Alveolar Ridges Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy Of Alveolar Ridges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Optic Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Optic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Scapular Muscle Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Scapular Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Intrinsic Hand Muscle Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intrinsic Hand Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Pontocerebellar Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pontocerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Tubular Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tubular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Tubular Atrophy Assessment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tubular Atrophy Assessment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Peripapillary Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripapillary Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Tibialis Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tibialis Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fundus Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fundus Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Levator Palpebrae Superioris Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Levator Palpebrae Superioris Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Superior Rectus Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Superior Rectus Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Frontal Lobe Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Frontal Lobe Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Axial Muscle Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Axial Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy/Degeneration Involving The Spinal Cord Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy/Degeneration Involving The Spinal Cord in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy Of Vas Deferens Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy Of Vas Deferens in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy/Degeneration Affecting The Central Nervous System Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy/Degeneration Affecting The Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy/Degeneration Affecting The Cerebrum Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy/Degeneration Affecting The Cerebrum in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
skeletal muscle atrophy Gene Set From GO Biological Process Annotations 2023 genes participating in the skeletal muscle atrophy biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of muscle atrophy Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of muscle atrophy biological process from the curated GO Biological Process Annotations 2023 dataset.
striated muscle atrophy Gene Set From GO Biological Process Annotations 2023 genes participating in the striated muscle atrophy biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of muscle atrophy Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of muscle atrophy biological process from the curated GO Biological Process Annotations 2023 dataset.
muscular atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the muscular atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Meibomian gland atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the Meibomian gland atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
renal glomerulus atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the renal glomerulus atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
temporal lobe atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the temporal lobe atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
alveolar process atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the alveolar process atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
kidney atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the kidney atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
testicular atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the testicular atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
thymus atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the thymus atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

Harmonizome 3.0

atrophy; prenatal exposure delayed effects; substance-related disorders Gene Set

folic acid deficiency; pregnancy complications; prenatal exposure delayed effects; psychomotor disorders; vitamin b 12 deficiency Gene Set

memory disorders; prenatal exposure delayed effects Gene Set

alcohol-induced disorders; prenatal exposure delayed effects Gene Set

birth weight; fetal diseases; nutrition disorders; osteoporosis; prenatal exposure delayed effects Gene Set

Prenatal Exposure Delayed Effects Gene Set

asthma; prenatal exposure delayed effects; respiratory sounds Gene Set

pregnancy complications; prenatal exposure delayed effects; serotonin syndrome Gene Set

prenatal exposure delayed effects; respiratory tract diseases Gene Set

inflammation; prenatal exposure delayed effects; recurrence; respiratory sounds Gene Set

leukemia; prenatal exposure delayed effects Gene Set

asthma; prenatal exposure delayed effects Gene Set

abnormalities, drug-induced; epilepsy; prenatal exposure delayed effects Gene Set

birth weight; prenatal exposure delayed effects Gene Set

lead poisoning; prenatal exposure delayed effects Gene Set

dermatitis, atopic; eczema allergic; prenatal exposure delayed effects Gene Set

cleft palate; prenatal exposure delayed effects Gene Set

hiv infections; prenatal exposure delayed effects Gene Set

pregnancy complications; prenatal exposure delayed effects Gene Set

cleft lip; cleft palate; prenatal exposure delayed effects Gene Set

leukemia, lymphocytic, acute, l1; precursor cell lymphoblastic leukemia-lymphoma; prenatal exposure delayed effects Gene Set

birth weight; cerebral palsy; intracranial thrombosis; obstetric labor complications; prenatal exposure delayed effects Gene Set

heart defects, congenital; hyperhomocysteinemia; prenatal exposure delayed effects Gene Set

asthma; prenatal exposure delayed effects; respiratory hypersensitivity; respiratory sounds Gene Set

prenatal exposure delayed effects; starvation Gene Set

acute lymphocytic leukemia; precursor cell lymphoblastic leukemia-lymphoma; prenatal exposure delayed effects Gene Set

birth weight; fetal growth retardation; prenatal exposure delayed effects Gene Set

prenatal exposure delayed effects Gene Set

Prenatal Exposure Delayed Effects Gene Set

Prenatal Exposure Delayed Effects Gene Set

prenatal environment exposure Gene Set

Prenatal Alcohol Exposure Gene Set

Neurobehavioral disorder with prenatal alcohol exposure Gene Set

Motor development (prenatal lead exposure interaction) Gene Set

Mental development (prenatal lead exposure interaction) Gene Set

Organic Mental Disorders, Substance-Induced Gene Set

growth disorders; puberty, delayed Gene Set

muscular atrophy, spinal; spinal muscular atrophy Gene Set

muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy Gene Set

optic atrophy, autosomal dominant; optic atrophy, hereditary, leber Gene Set

optic atrophies, hereditary; optic atrophy, autosomal dominant; optic atrophy, hereditary, leber Gene Set

Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome Gene Set

atrophy; disorders Gene Set

alzheimer disease; atrophy; dementia; memory disorders Gene Set

atrophy; memory disorders Gene Set

alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders Gene Set

optic atrophy, hereditary, leber; vision disorders Gene Set

dystonic disorders; multiple system atrophy 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

fatigue; sleep disorders; sleep initiation and maintenance 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

Prenatal Injuries Gene Set

prenatal viability Gene Set

breast cancer risk and prenatal viability Gene Set

prenatal Gene Set

abnormality of prenatal development or birth Gene Set

prenatal maternal abnormality Gene Set

abnormality of prenatal development or birth Gene Set

multiple prenatal fractures Gene Set

prenatal maternal abnormality Gene Set

prenatal movement abnormality Gene Set

abnormal prenatal growth/weight/body size Gene Set

partial prenatal lethality Gene Set

prenatal growth retardation Gene Set

complete prenatal lethality Gene Set

abnormal prenatal body size Gene Set

prenatal lethality Gene Set

Prenatal Maternal Abnormality Gene Set

Abnormality Of Prenatal Development Or Birth Gene Set