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Alcohol Related Birth Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol Related Birth Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
alcohol-related birth defect Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alcohol-related birth defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
birth weight; fetal alcohol syndrome; fetal growth retardation; intrauterine growth retardation; syndrome; fetal, alcohol (dysmorphic) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; fetal alcohol syndrome; fetal growth retardation; intrauterine growth retardation; syndrome; fetal, alcohol (dysmorphic) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol-related birth defects Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease alcohol-related birth defects in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Alcohol dependence or chronic alcoholic pancreatitis or alcohol-related liver cirrhosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol dependence or chronic alcoholic pancreatitis or alcohol-related liver cirrhosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
birth weight; infant, newborn, diseases; infection; premature birth Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; infant, newborn, diseases; infection; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; premature birth Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Spontaneous preterm birth (preterm birth) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Spontaneous preterm birth (preterm birth) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
alcohol-related disorders; cocaine-related disorders; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol-related disorders; cocaine-related disorders; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cocaine-related disorders; opioid-related disorders; substance-related disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cocaine-related disorders; opioid-related disorders; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fetal alcohol syndrome; syndrome; fetal, alcohol (dysmorphic) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fetal alcohol syndrome; syndrome; fetal, alcohol (dysmorphic) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
delirium tremens, alcohol withdrawal-induced; seizures, alcohol withdrawal-induced Gene SetFrom GAD Gene-Disease Associations genes associated with the disease delirium tremens, alcohol withdrawal-induced; seizures, alcohol withdrawal-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol withdrawal delirium; alcohol withdrawal seizures Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol withdrawal delirium; alcohol withdrawal seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
delirium tremens, alcohol-induced; alcohol withdrawal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease delirium tremens, alcohol-induced; alcohol withdrawal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
MPV17-related mitochondrial DNA maintenance defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the MPV17-related mitochondrial DNA maintenance defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Alcohol-Related Disorders Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alcohol-Related Disorders from the curated CTD Gene-Disease Associations dataset. |
alcohol-related neurodevelopmental disorder Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alcohol-related neurodevelopmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
alcohol-related disorders; neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol-related disorders; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol-related disorders; carcinoma, squamous cell; head and neck neoplasms; squamous cell carcinoma; tobacco use disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol-related disorders; carcinoma, squamous cell; head and neck neoplasms; squamous cell carcinoma; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol-related polyneuropathy; alcoholic neuropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol-related polyneuropathy; alcoholic neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol-related disorders; alcoholism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol-related disorders; alcoholism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol-related disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Alcohol-Related Disorders Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Alcohol-Related Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
{aerodigestive tract cancer, squamous cell, alcohol-related, protection against} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {aerodigestive tract cancer, squamous cell, alcohol-related, protection against} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{esophageal cancer, alcohol-related, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {esophageal cancer, alcohol-related, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
Alcohol-Related Liver Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol-Related Liver Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alcohol Related Neurodevelopmental Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol Related Neurodevelopmental Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Esophageal Cancer, Alcohol-Related, Susceptibility To Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Esophageal Cancer, Alcohol-Related, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aerodigestive Tract Cancer, Squamous Cell, Alcohol-Related, Protection Against Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aerodigestive Tract Cancer, Squamous Cell, Alcohol-Related, Protection Against in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
alcohol-related neurodevelopmental disorder Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease alcohol-related neurodevelopmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Cirrhosis (alcohol related) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cirrhosis (alcohol related) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol-related hepatocellular carcinoma Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol-related hepatocellular carcinoma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
alcoholism; opioid-related disorders; substance-related disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcoholism; opioid-related disorders; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcoholism; cocaine-related disorders; heroin dependence; substance-related disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcoholism; cocaine-related disorders; heroin dependence; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anticoagulant complications; bleeding events, warfarin therapy-related; overanticoagulation, warfarin therapy-related Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anticoagulant complications; bleeding events, warfarin therapy-related; overanticoagulation, warfarin therapy-related in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Actin-related protein 8/Plant actin-related protein 9 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Actin-related protein 8/Plant actin-related protein 9 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Hepatitis B virus-related hepatocellular carcinoma vs hepatitis B virus-related decompensated cirrhosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hepatitis B virus-related hepatocellular carcinoma vs hepatitis B virus-related decompensated cirrhosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Premature Birth Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Premature Birth from the curated CTD Gene-Disease Associations dataset. |
Birth Weight Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Birth Weight from the curated CTD Gene-Disease Associations dataset. |
Birth Weight Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Birth Weight in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
birth weight; hemochromatosis; precursor cell lymphoblastic leukemia-lymphoma; pregnancy complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; hemochromatosis; precursor cell lymphoblastic leukemia-lymphoma; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; growth disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; growth disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, spontaneous; premature birth Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, spontaneous; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
premature birth; vaginosis, bacterial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease premature birth; vaginosis, bacterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; insulin resistance; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; hyperbilirubinemia, neonatal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; hyperbilirubinemia, neonatal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chorioamnionitis; inflammation; premature birth Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chorioamnionitis; inflammation; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; respiratory distress syndrome, newborn Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; respiratory distress syndrome, newborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; growth disorders; insulin resistance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; growth disorders; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; hemorrhage; pregnancy complications, cardiovascular; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; hemorrhage; pregnancy complications, cardiovascular; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; diabetes mellitus, type 2; insulin resistance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; diabetes mellitus, type 2; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; fetal growth retardation; intrauterine growth retardation; vitamin d deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; fetal growth retardation; intrauterine growth retardation; vitamin d deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; pregnancy complications, cardiovascular; premature birth; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; pregnancy complications, cardiovascular; premature birth; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
insulin; obesity; birth weight Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin; obesity; birth weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
premature birth; uterine cervical incompetence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease premature birth; uterine cervical incompetence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fetal membranes, premature rupture; premature birth; uterine prolapse Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fetal membranes, premature rupture; premature birth; uterine prolapse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; diabetes, type 2; leukemia; breast cancer; glucose; cytogenetic studies; birth weight; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; diabetes, type 2; leukemia; breast cancer; glucose; cytogenetic studies; birth weight; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
inflammation; premature birth Gene SetFrom GAD Gene-Disease Associations genes associated with the disease inflammation; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
muscle testing; birth weight Gene SetFrom GAD Gene-Disease Associations genes associated with the disease muscle testing; birth weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight preterm delivery Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight preterm delivery in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
spontaneous preterm birth Gene SetFrom GAD Gene-Disease Associations genes associated with the disease spontaneous preterm birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; leukemia; leukemia, myeloid, acute; precursor cell lymphoblastic leukemia-lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; leukemia; leukemia, myeloid, acute; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; sudden infant death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; diabetes mellitus type ii; diabetes mellitus, type 2 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; chorioamnionitis; infection; inflammation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; chorioamnionitis; infection; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; pregnancy complications, hematologic; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; diabetes mellitus, type 1 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; diabetes mellitus, type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; insulin resistance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fetal death; pre-eclampsia; pregnancy complications; premature birth Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fetal death; pre-eclampsia; pregnancy complications; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; weight gain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth defects Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; pre-eclampsia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; pre-eclampsia; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; pre-eclampsia; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
premature birth; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease premature birth; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
size at birth Gene SetFrom GAD Gene-Disease Associations genes associated with the disease size at birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chorioamnionitis; premature birth Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chorioamnionitis; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; hyperglycemia; pregnancy complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; hyperglycemia; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; fetal growth retardation; placental insufficiency; pre-eclampsia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; fetal growth retardation; placental insufficiency; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; cardiovascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; cardiovascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infection; inflammation; premature birth Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infection; inflammation; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glucose; birth weight Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glucose; birth weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; hemochromatosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; hemochromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
premature birth Gene SetFrom GAD Gene-Disease Associations genes associated with the disease premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; post-partum bleeding; postpartum hemorrhage; pregnancy complications, hematologic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; post-partum bleeding; postpartum hemorrhage; pregnancy complications, hematologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; prenatal exposure delayed effects Gene SetFrom 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. |
birth weight; diabetes mellitus, type 1; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; diabetes mellitus, type 1; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; retinopathy of prematurity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; retinopathy of prematurity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hemorrhage; placenta diseases; premature birth; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hemorrhage; placenta diseases; premature birth; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bacterial vaginosis; premature birth; vaginosis, bacterial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bacterial vaginosis; premature birth; vaginosis, bacterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; diabetes mellitus type ii; diabetes mellitus, type 2; thinness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; diabetes mellitus type ii; diabetes mellitus, type 2; thinness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; fetal growth retardation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; fetal growth retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infection; premature birth Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infection; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; diabetes mellitus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; diabetes mellitus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth height growth to adolescence and adult stature Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth height growth to adolescence and adult stature in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; cord blood igf-ii levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; cord blood igf-ii levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy complications, hematologic; premature birth; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy complications, hematologic; premature birth; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; birth weight; height Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; birth weight; height in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight and serum triglyceride concentration Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight and serum triglyceride concentration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; preterm delivery Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; preterm delivery in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; cardiovascular diseases; metabolic syndrome x; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; cardiovascular diseases; metabolic syndrome x; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dental plaque; periodontitis; pregnancy complications; premature birth Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dental plaque; periodontitis; pregnancy complications; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; critical illness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; critical illness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; body weight Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; body weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; lipid metabolism, inborn errors Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; lipid metabolism, inborn errors 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 SetFrom 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. |
connective tissue diseases; fetal diseases; inflammation; musculoskeletal diseases; pregnancy complications, hematologic; premature birth; skin diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease connective tissue diseases; fetal diseases; inflammation; musculoskeletal diseases; pregnancy complications, hematologic; premature birth; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; vitamin d deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; vitamin d deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 2; cardiovascular disease; birth weight Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 2; cardiovascular disease; birth weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; placental weight Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; placental weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chorioamnionitis; infection of amniotic sac and membranes; premature birth Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chorioamnionitis; infection of amniotic sac and membranes; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; spinal osteophytosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; spinal osteophytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; diabetes, gestational; gestational diabetes mellitus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; diabetes, gestational; gestational diabetes mellitus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ductus arteriosus, patent; patent ductus arteriosus; premature birth Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ductus arteriosus, patent; patent ductus arteriosus; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 2; obesity; birth weight Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 2; obesity; birth weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
preterm birth Gene SetFrom GAD Gene-Disease Associations genes associated with the disease preterm birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; diabetes, type 2; glucose; birth weight Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; diabetes, type 2; glucose; birth weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fetal membranes, premature rupture; premature birth Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fetal membranes, premature rupture; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; cystic fibrosis; ileus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; cystic fibrosis; ileus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; hyperglycemia; pregnancy complications; pregnancy in diabetics Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; hyperglycemia; pregnancy complications; pregnancy in diabetics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; hellp syndrome; pre-eclampsia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; hellp syndrome; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; fetal growth retardation; intrauterine growth retardation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; fetal growth retardation; intrauterine growth retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chorioamnionitis; fetal membranes, premature rupture; infection of amniotic sac and membranes; obstetric labor, premature; pre-eclampsia; premature birth Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chorioamnionitis; fetal membranes, premature rupture; infection of amniotic sac and membranes; obstetric labor, premature; pre-eclampsia; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; fetal growth retardation; prenatal exposure delayed effects Gene SetFrom 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. |
obesity; birth weight Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obesity; birth weight 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 SetFrom 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. |
birth weight; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term birth in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
embryo development ending in birth or egg hatching Gene SetFrom GO Biological Process Annotations 2015 genes participating in the embryo development ending in birth or egg hatching biological process from the curated GO Biological Process Annotations 2015 dataset. |
Birth weight Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Birth weight phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
abnormality of prenatal development or birth Gene SetFrom 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. |
birth length less than 3rd percentile Gene SetFrom HPO Gene-Disease Associations genes associated with the birth length less than 3rd percentile phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
two carpal ossification centers present at birth Gene SetFrom HPO Gene-Disease Associations genes associated with the two carpal ossification centers present at birth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of prenatal development or birth Gene SetFrom 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. |
premature birth following premature rupture of fetal membranes Gene SetFrom HPO Gene-Disease Associations genes associated with the premature birth following premature rupture of fetal membranes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
birth length greater than 97th percentile Gene SetFrom HPO Gene-Disease Associations genes associated with the birth length greater than 97th percentile phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
premature birth Gene SetFrom HPO Gene-Disease Associations genes associated with the premature birth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
desquamation of skin soon after birth Gene SetFrom HPO Gene-Disease Associations genes associated with the desquamation of skin soon after birth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
femoral bowing present at birth, straightening with time Gene SetFrom HPO Gene-Disease Associations genes associated with the femoral bowing present at birth, straightening with time phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
generalized muscular appearance from birth Gene SetFrom HPO Gene-Disease Associations genes associated with the generalized muscular appearance from birth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Premature Birth Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Premature Birth phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Birth Weight Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Birth Weight phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
increased birth body size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased birth body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
eyelids open at birth Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the eyelids open at birth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal birth body size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal birth body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased birth weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased birth weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased birth body size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased birth body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal birth weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal birth weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased birth weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased birth weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
[birth weight qtl 2] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [birth weight qtl 2] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[birth weight qtl 3] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [birth weight qtl 3] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[birth weight qtl 1] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [birth weight qtl 1] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[birth weight qtl4] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [birth weight qtl4] phenotype from the curated OMIM Gene-Disease Associations dataset. |
Infant, Very Low Birth Weight Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Infant, Very Low Birth Weight in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of Prenatal Development Or Birth Gene SetFrom 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. |
Patent Ductus Arteriosus After Birth At Term Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Patent Ductus Arteriosus After Birth At Term in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Premature Birth Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Premature Birth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Birth Weight Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Birth Weight in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Very Low Birth Weight Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Very Low Birth Weight in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Desquamation Of Skin Soon After Birth Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Desquamation Of Skin Soon After Birth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Birth Length Less Than 3Rd Percentile Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Birth Length Less Than 3Rd Percentile in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Generalized Muscular Appearance From Birth Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Muscular Appearance From Birth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Infant, Extremely Low Birth Weight Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infant, Extremely Low Birth Weight in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cephalhematoma Due To Birth Trauma Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cephalhematoma Due To Birth Trauma in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Premature Birth Following Premature Rupture Of Fetal Membranes Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Premature Birth Following Premature Rupture Of Fetal Membranes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Femoral Bowing Present At Birth, Straightening With Time Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Femoral Bowing Present At Birth, Straightening With Time in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Birth Length Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Birth Length in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Birth Length Greater Than 97Th Percentile Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Birth Length Greater Than 97Th Percentile in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Two Carpal Ossification Centers Present At Birth Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Two Carpal Ossification Centers Present At Birth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Red, Cracking, Peeling Skin At Birth Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Red, Cracking, Peeling Skin At Birth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
embryo development ending in birth or egg hatching Gene SetFrom GO Biological Process Annotations 2023 genes participating in the embryo development ending in birth or egg hatching biological process from the curated GO Biological Process Annotations 2023 dataset. |
decreased birth body size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased birth body size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
eyelids open at birth Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the eyelids open at birth phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased birth weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased birth weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased birth body size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased birth body size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased birth weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased birth weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
embryo development ending in birth or egg hatching Gene SetFrom GO Biological Process Annotations 2025 genes participating in the embryo development ending in birth or egg hatching biological process from the curated GO Biological Process Annotations 2025 dataset. |
Abnormality of prenatal development or birth Gene SetFrom 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. |
Premature birth Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Premature birth phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
spontaneous preterm birth x maternal stress interaction (1df) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the spontaneous preterm birth x maternal stress interaction (1df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Age at first birth Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age at first birth phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Gestational age at birth (maternal effect) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gestational age at birth (maternal effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Gestational age at birth in premature rupture of membrane-initiated deliveries (maternal effect) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gestational age at birth in premature rupture of membrane-initiated deliveries (maternal effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Preterm birth (maternal effect) (maternal pre-pregnancy BMI interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Preterm birth (maternal effect) (maternal pre-pregnancy BMI interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Spontaneous preterm birth (maternal effect) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Spontaneous preterm birth (maternal effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Birth length Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Birth length phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Birth weight Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Birth weight phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Spontaneous preterm birth (preterm delivery) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Spontaneous preterm birth (preterm delivery) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Offspring birth weight Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Offspring birth weight phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Preterm birth (maternal effect) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Preterm birth (maternal effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
BMI at birth Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the BMI at birth phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Moderate-to-late spontaneous preterm birth Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Moderate-to-late spontaneous preterm birth phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Spontaneous preterm birth with premature rupture of membranes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Spontaneous preterm birth with premature rupture of membranes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Spontaneous preterm birth without premature rupture of membranes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Spontaneous preterm birth without premature rupture of membranes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Gestational age at birth (child effect) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gestational age at birth (child effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Early spontaneous preterm birth Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Early spontaneous preterm birth phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Post-term birth Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Post-term birth phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Birth weight variance Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Birth weight variance phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Dandy-Walker like malformation with atrioventricular septal defect Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dandy-Walker like malformation with atrioventricular septal defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Protan defect Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Protan defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cardiac conduction defect, nonspecific Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cardiac conduction defect, nonspecific phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atrial septal defect 7 with or without atrioventricular conduction defects Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atrial septal defect 7 with or without atrioventricular conduction defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Phosphate transport defect Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Phosphate transport defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Neutral 1 amino acid transport defect Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neutral 1 amino acid transport defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ventricular septal defect 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ventricular septal defect 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ventricular septal defect 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ventricular septal defect 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atrial septal defect 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atrial septal defect 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Laron-type isolated somatotropin defect Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Laron-type isolated somatotropin defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Neural tube defect Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neural tube defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atrioventricular septal defect, partial, with heterotaxy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atrioventricular septal defect, partial, with heterotaxy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bile acid synthesis defect, congenital, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bile acid synthesis defect, congenital, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bile acid synthesis defect, congenital, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bile acid synthesis defect, congenital, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glucose-6-phosphate transport defect Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glucose-6-phosphate transport defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Iodotyrosine deiodination defect Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Iodotyrosine deiodination defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thrombophilia due to thrombomodulin defect Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thrombophilia due to thrombomodulin defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal carnitine transport defect Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal carnitine transport defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atrioventricular septal defect 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atrioventricular septal defect 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atrioventricular septal defect 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atrioventricular septal defect 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Immunodeficiency due to defect in cd3-zeta Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Immunodeficiency due to defect in cd3-zeta phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Erythrocyte lactate transporter defect Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Erythrocyte lactate transporter defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atrial septal defect 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atrial septal defect 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atrial septal defect 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atrial septal defect 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Atrial septal defect 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Atrial septal defect 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital defect of folate absorption Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital defect of folate absorption phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Oocyte maturation defect Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Oocyte maturation defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Immune dysfunction with T-cell inactivation due to calcium entry defect 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Immune dysfunction with T-cell inactivation due to calcium entry defect 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Immune dysfunction with T-cell inactivation due to calcium entry defect 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Immune dysfunction with T-cell inactivation due to calcium entry defect 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Iodotyrosyl coupling defect Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Iodotyrosyl coupling defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thrombophilia, X-Linked, Due To Factor Ix Defect Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Thrombophilia, X-Linked, Due To Factor Ix Defect from the curated CTD Gene-Disease Associations dataset. |
Sacral defect and anterior sacral meningocele Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sacral defect and anterior sacral meningocele from the curated CTD Gene-Disease Associations dataset. |
Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type from the curated CTD Gene-Disease Associations dataset. |
Cardiac Conduction Defect Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiac Conduction Defect from the curated CTD Gene-Disease Associations dataset. |
Atrial septal defect 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Atrial septal defect 2 from the curated CTD Gene-Disease Associations dataset. |
ATRIOVENTRICULAR SEPTAL DEFECT 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease ATRIOVENTRICULAR SEPTAL DEFECT 3 from the curated CTD Gene-Disease Associations dataset. |
Atrioventricular Septal Defect, Partial, with Heterotaxy Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Atrioventricular Septal Defect, Partial, with Heterotaxy Syndrome from the curated CTD Gene-Disease Associations dataset. |
Bile acid synthesis defect, congenital, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bile acid synthesis defect, congenital, 2 from the curated CTD Gene-Disease Associations dataset. |
Bile acid synthesis defect, congenital, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bile acid synthesis defect, congenital, 4 from the curated CTD Gene-Disease Associations dataset. |
METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT from the curated CTD Gene-Disease Associations dataset. |
Atrial Septal Defect 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Septal Defect 4 from the curated CTD Gene-Disease Associations dataset. |
Atrioventricular Canal Defect Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Atrioventricular Canal Defect from the curated CTD Gene-Disease Associations dataset. |
Bile acid synthesis defect, congenital, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bile acid synthesis defect, congenital, 1 from the curated CTD Gene-Disease Associations dataset. |
Neural tube defect, folate-sensitive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neural tube defect, folate-sensitive from the curated CTD Gene-Disease Associations dataset. |
Atrial Septal Defect 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Septal Defect 6 from the curated CTD Gene-Disease Associations dataset. |
NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT from the curated CTD Gene-Disease Associations dataset. |
Immunodeficiency due to Defect in CD3-Zeta Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Immunodeficiency due to Defect in CD3-Zeta from the curated CTD Gene-Disease Associations dataset. |
Atrial Septal Defect 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Septal Defect 5 from the curated CTD Gene-Disease Associations dataset. |
Atrial Septal Defect 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Septal Defect 1 from the curated CTD Gene-Disease Associations dataset. |
Erythrocyte Lactate Transporter Defect Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Erythrocyte Lactate Transporter Defect from the curated CTD Gene-Disease Associations dataset. |
Immunodeficiency due to Defect in MAPBP-Interacting Protein Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Immunodeficiency due to Defect in MAPBP-Interacting Protein from the curated CTD Gene-Disease Associations dataset. |
Immune dysfunction with T-cell inactivation due to calcium entry defect 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Immune dysfunction with T-cell inactivation due to calcium entry defect 1 from the curated CTD Gene-Disease Associations dataset. |
Immune dysfunction with T-cell inactivation due to calcium entry defect 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Immune dysfunction with T-cell inactivation due to calcium entry defect 2 from the curated CTD Gene-Disease Associations dataset. |
ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS from the curated CTD Gene-Disease Associations dataset. |
atrial heart septal defect Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease atrial heart septal defect from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
heart septal defect Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease heart septal defect from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
heart septal defect Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease heart septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
ventricular septal defect Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ventricular septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
atrioventricular septal defect Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease atrioventricular septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
congenital bile acid synthesis defect Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital bile acid synthesis defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
atrial heart septal defect Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease atrial heart septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
qualitative platelet defect Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease qualitative platelet defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
human spermatogenic defect Gene SetFrom GAD Gene-Disease Associations genes associated with the disease human spermatogenic defect in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
defect Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term defect in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
conotruncal defect Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the conotruncal defect phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
thyroid hormone receptor defect Gene SetFrom HPO Gene-Disease Associations genes associated with the thyroid hormone receptor defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
ventricular septal defect Gene SetFrom HPO Gene-Disease Associations genes associated with the ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
midline defect of mandible Gene SetFrom HPO Gene-Disease Associations genes associated with the midline defect of mandible phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
vertebral segmentation defect Gene SetFrom HPO Gene-Disease Associations genes associated with the vertebral segmentation defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
electron transfer flavoprotein-ubiquinone oxidoreductase defect Gene SetFrom HPO Gene-Disease Associations genes associated with the electron transfer flavoprotein-ubiquinone oxidoreductase defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
secundum atrial septal defect Gene SetFrom HPO Gene-Disease Associations genes associated with the secundum atrial septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
dynein arm defect of respiratory motile cilia Gene SetFrom HPO Gene-Disease Associations genes associated with the dynein arm defect of respiratory motile cilia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
inlet ventricular septal defect Gene SetFrom HPO Gene-Disease Associations genes associated with the inlet ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thyroid defect in oxidation and organification of iodide Gene SetFrom HPO Gene-Disease Associations genes associated with the thyroid defect in oxidation and organification of iodide phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
adrenocorticotropin (acth) receptor (acthr) defect Gene SetFrom HPO Gene-Disease Associations genes associated with the adrenocorticotropin (acth) receptor (acthr) defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
sacral segmentation defect Gene SetFrom HPO Gene-Disease Associations genes associated with the sacral segmentation defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abdominal wall defect Gene SetFrom HPO Gene-Disease Associations genes associated with the abdominal wall defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
visual field defect Gene SetFrom HPO Gene-Disease Associations genes associated with the visual field defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atrioventricular canal defect with right ventricle aorta and pulmonary atresia Gene SetFrom HPO Gene-Disease Associations genes associated with the atrioventricular canal defect with right ventricle aorta and pulmonary atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
muscular ventricular septal defect Gene SetFrom HPO Gene-Disease Associations genes associated with the muscular ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
defect in the atrial septum Gene SetFrom HPO Gene-Disease Associations genes associated with the defect in the atrial septum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
congenital septal defect Gene SetFrom HPO Gene-Disease Associations genes associated with the congenital septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
skull defect Gene SetFrom HPO Gene-Disease Associations genes associated with the skull defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
generalized hypotonia due to defect at the neuromuscular junction Gene SetFrom HPO Gene-Disease Associations genes associated with the generalized hypotonia due to defect at the neuromuscular junction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cervical segmentation defect Gene SetFrom HPO Gene-Disease Associations genes associated with the cervical segmentation defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atrioventricular canal defect Gene SetFrom HPO Gene-Disease Associations genes associated with the atrioventricular canal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
perimembranous ventricular septal defect Gene SetFrom HPO Gene-Disease Associations genes associated with the perimembranous ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
midline defect of the nose Gene SetFrom HPO Gene-Disease Associations genes associated with the midline defect of the nose phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
complete atrioventricular canal defect Gene SetFrom HPO Gene-Disease Associations genes associated with the complete atrioventricular canal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
large central visual field defect Gene SetFrom HPO Gene-Disease Associations genes associated with the large central visual field defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
conotruncal defect Gene SetFrom HPO Gene-Disease Associations genes associated with the conotruncal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
primum atrial septal defect Gene SetFrom HPO Gene-Disease Associations genes associated with the primum atrial septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Mannose-P-dolichol utilization defect 1 protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Mannose-P-dolichol utilization defect 1 protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
atrial septal defect Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the atrial septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ventricular septal defect Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
perimembraneous ventricular septal defect Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the perimembraneous ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
partial atrioventricular septal defect Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the partial atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
inlet ventricular septal defect Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the inlet ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
double outlet right ventricle with atrioventricular septal defect Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the double outlet right ventricle with atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
iodide oxidation defect Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the iodide oxidation defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
aorticopulmonary septal defect Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the aorticopulmonary septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
double outlet right ventricle, ventricular defect committed to aorta Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the double outlet right ventricle, ventricular defect committed to aorta phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
muscular ventricular septal defect Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the muscular ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ostium primum atrial septal defect Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ostium primum atrial septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
complete atrioventricular septal defect Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the complete atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ostium secundum atrial septal defect Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ostium secundum atrial septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
atrioventricular septal defect Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thrombophilia due to thrombomodulin defect Gene SetFrom OMIM Gene-Disease Associations genes associated with the thrombophilia due to thrombomodulin defect phenotype from the curated OMIM Gene-Disease Associations dataset. |
bleeding disorder due to p2rx1 defect Gene SetFrom OMIM Gene-Disease Associations genes associated with the bleeding disorder due to p2rx1 defect phenotype from the curated OMIM Gene-Disease Associations dataset. |
schizophrenia, neurophysiologic defect in Gene SetFrom OMIM Gene-Disease Associations genes associated with the schizophrenia, neurophysiologic defect in phenotype from the curated OMIM Gene-Disease Associations dataset. |
{atrioventricular septal defect, susceptibility to, 1} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {atrioventricular septal defect, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset. |
?isolated growth hormone deficiency due to defect in ghrf Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?isolated growth hormone deficiency due to defect in ghrf phenotype from the curated OMIM Gene-Disease Associations dataset. |
erythrocyte lactate transporter defect Gene SetFrom OMIM Gene-Disease Associations genes associated with the erythrocyte lactate transporter defect phenotype from the curated OMIM Gene-Disease Associations dataset. |
natural killer cell and glucocorticoid deficiency with dna repair defect Gene SetFrom OMIM Gene-Disease Associations genes associated with the natural killer cell and glucocorticoid deficiency with dna repair defect phenotype from the curated OMIM Gene-Disease Associations dataset. |
ventricular septal defect 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ventricular septal defect 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
ventricular septal defect 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ventricular septal defect 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
selective t-cell defect Gene SetFrom OMIM Gene-Disease Associations genes associated with the selective t-cell defect phenotype from the curated OMIM Gene-Disease Associations dataset. |
{hypercholesterolemia, familial, due to ldlr defect, modifier of} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {hypercholesterolemia, familial, due to ldlr defect, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset. |
atrial septal defect 6 Gene SetFrom OMIM Gene-Disease Associations genes associated with the atrial septal defect 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
atrial septal defect 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the atrial septal defect 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
atrial septal defect 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the atrial septal defect 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
atrial septal defect 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the atrial septal defect 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
atrial septal defect 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the atrial septal defect 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
atrial septal defect 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the atrial septal defect 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
atrial septal defect 9 Gene SetFrom OMIM Gene-Disease Associations genes associated with the atrial septal defect 9 phenotype from the curated OMIM Gene-Disease Associations dataset. |
atrial septal defect 8 Gene SetFrom OMIM Gene-Disease Associations genes associated with the atrial septal defect 8 phenotype from the curated OMIM Gene-Disease Associations dataset. |
atrioventricular septal defect, partial, with heterotaxy syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the atrioventricular septal defect, partial, with heterotaxy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
bile acid synthesis defect, congenital, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the bile acid synthesis defect, congenital, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
bile acid synthesis defect, congenital, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the bile acid synthesis defect, congenital, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
bile acid synthesis defect, congenital, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the bile acid synthesis defect, congenital, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
bile acid synthesis defect, congenital, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the bile acid synthesis defect, congenital, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
ventricular septal defect 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ventricular septal defect 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cardiac conduction defect, nonspecific Gene SetFrom OMIM Gene-Disease Associations genes associated with the cardiac conduction defect, nonspecific phenotype from the curated OMIM Gene-Disease Associations dataset. |
rickets due to defect in vitamin d 25-hydroxylation Gene SetFrom OMIM Gene-Disease Associations genes associated with the rickets due to defect in vitamin d 25-hydroxylation phenotype from the curated OMIM Gene-Disease Associations dataset. |
{atrioventricular septal defect, susceptibility to, 2} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {atrioventricular septal defect, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset. |
oocyte maturation defect Gene SetFrom OMIM Gene-Disease Associations genes associated with the oocyte maturation defect phenotype from the curated OMIM Gene-Disease Associations dataset. |
methylmalonic aciduria due to transcobalamin receptor defect Gene SetFrom OMIM Gene-Disease Associations genes associated with the methylmalonic aciduria due to transcobalamin receptor defect phenotype from the curated OMIM Gene-Disease Associations dataset. |
atrioventricular septal defect 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the atrioventricular septal defect 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
atrioventricular septal defect 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the atrioventricular septal defect 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
atrioventricular septal defect 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the atrioventricular septal defect 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
thrombophilia, x-linked, due to factor ix defect Gene SetFrom OMIM Gene-Disease Associations genes associated with the thrombophilia, x-linked, due to factor ix defect phenotype from the curated OMIM Gene-Disease Associations dataset. |
atrial septal defect 7, with or without av conduction defects Gene SetFrom OMIM Gene-Disease Associations genes associated with the atrial septal defect 7, with or without av conduction defects phenotype from the curated OMIM Gene-Disease Associations dataset. |
immunodeficiency due to defect in mapbp-interacting protein Gene SetFrom OMIM Gene-Disease Associations genes associated with the immunodeficiency due to defect in mapbp-interacting protein phenotype from the curated OMIM Gene-Disease Associations dataset. |
goiter, familial, due to ttf-1 defect Gene SetFrom OMIM Gene-Disease Associations genes associated with the goiter, familial, due to ttf-1 defect phenotype from the curated OMIM Gene-Disease Associations dataset. |
immunodeficiency, x-linked, with magnesium defect, epstein-barr virus infection and neoplasia Gene SetFrom OMIM Gene-Disease Associations genes associated with the immunodeficiency, x-linked, with magnesium defect, epstein-barr virus infection and neoplasia phenotype from the curated OMIM Gene-Disease Associations dataset. |
thrombophilia due to thrombin defect Gene SetFrom OMIM Gene-Disease Associations genes associated with the thrombophilia due to thrombin defect phenotype from the curated OMIM Gene-Disease Associations dataset. |
{cardiac conduction defect, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {cardiac conduction defect, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
methylmalonic aciduria, vitamin b12-responsive, due to defect in synthesis of adenosylcobalamin, cblb complementation type Gene SetFrom OMIM Gene-Disease Associations genes associated with the methylmalonic aciduria, vitamin b12-responsive, due to defect in synthesis of adenosylcobalamin, cblb complementation type phenotype from the curated OMIM Gene-Disease Associations dataset. |
Defective CYP7B1 causes Spastic paraplegia 5A, autosomal recessive (SPG5A) and Congenital bile acid synthesis defect 3 (CBAS3) Gene Setproteins participating in the Defective CYP7B1 causes Spastic paraplegia 5A, autosomal recessive (SPG5A) and Congenital bile acid synthesis defect 3 (CBAS3) pathway from the Reactome Pathways dataset. |
Histidinuria Renal Tubular Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Histidinuria Renal Tubular Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bile Acid Synthesis Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bile Acid Synthesis Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Renal Carnitine Transport Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Renal Carnitine Transport Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrioventricular Canal Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrioventricular Canal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrioventricular Septal Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrioventricular Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortopulmonary Septal Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortopulmonary Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrial Septal Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrial Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ostium Secundum Atrial Septal Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ostium Secundum Atrial Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Glucose-6-Phosphate Transport Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Glucose-6-Phosphate Transport Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ventilatory Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ventilatory Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Calvarial Skull Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Calvarial Skull Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Single Ventricle Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Single Ventricle Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Defect Of Skull And Scalp Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Defect Of Skull And Scalp in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Coronary Sinus Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Coronary Sinus Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Muscular Ventricular Septum Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Muscular Ventricular Septum Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Perimembranous Ventricular Septal Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Perimembranous Ventricular Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Triple Gene Defect Alpha Thalassemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Triple Gene Defect Alpha Thalassemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Defect Of Vertebral Segmentation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Defect Of Vertebral Segmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Glycosylphosphatidylinositol Biosynthesis Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Glycosylphosphatidylinositol Biosynthesis Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cardiac Conduction Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cardiac Conduction Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Patent Or Persistent Ostium Secundum Defect (Type Ii) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Patent Or Persistent Ostium Secundum Defect (Type Ii) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Patent Or Persistent Sinus Venosus Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Patent Or Persistent Sinus Venosus Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Antibody Deficiency Due To Defect In Cd19 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Antibody Deficiency Due To Defect In Cd19 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Conotruncal Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Conotruncal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ventricular Septal Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ventricular Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Obstructive Ventilatory Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Obstructive Ventilatory Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrioventricular Septal Defect, Partial, With Heterotaxy Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrioventricular Septal Defect, Partial, With Heterotaxy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Partial Defect Of Atrioventricular Canal Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Partial Defect Of Atrioventricular Canal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Synthetic Defect Of Bile Acids Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Synthetic Defect Of Bile Acids in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Bile Acid Synthesis Defect Type 3 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Bile Acid Synthesis Defect Type 3 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Transitional Atrioventricular Canal Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Transitional Atrioventricular Canal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Bundle Branch System Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Bundle Branch System Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Midline Defect Of The Nose Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Midline Defect Of The Nose in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thyroid Hormone Plasma Membrane Transport Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thyroid Hormone Plasma Membrane Transport Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Defect Of Articular Cartilage Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Defect Of Articular Cartilage in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thoracoabdominal Wall Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thoracoabdominal Wall Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pulmonary Atresia With Ventricular Septal Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Atresia With Ventricular Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Membranous Ventricular Septum Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Membranous Ventricular Septum Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Defect Of The Pericardium Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Defect Of The Pericardium in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Insulin Receptor, Defect In Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Insulin Receptor, Defect In in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Iodide Transport Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Iodide Transport Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Neural Tube Defect, Folate-Sensitive Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Neural Tube Defect, Folate-Sensitive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Double Outlet Right Ventricle With Doubly Committed Ventricular Septal Defect And Pulmonary Stenosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Double Outlet Right Ventricle With Doubly Committed Ventricular Septal Defect And Pulmonary Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adenosylcobalamin Synthesis Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adenosylcobalamin Synthesis Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Oocyte Maturation Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Oocyte Maturation Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sacral Defect And Anterior Sacral Meningocele Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sacral Defect And Anterior Sacral Meningocele in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Renal Tubular Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Renal Tubular Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenitally Corrected Transposition Of The Great Arteries With Ventricular Septal Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenitally Corrected Transposition Of The Great Arteries With Ventricular Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cardiac Valvular Defect, Developmental Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cardiac Valvular Defect, Developmental in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ulnar-Fibular Ray Defect And Brachydactyly Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ulnar-Fibular Ray Defect And Brachydactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cardiac Conduction Defect, Nonprogressive Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cardiac Conduction Defect, Nonprogressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Corneal Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Corneal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fibrinolytic Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fibrinolytic Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Erythrocyte Lactate Transporter Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Erythrocyte Lactate Transporter Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mondini Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mondini Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Heart Defect, Tongue Hamartoma And Polysyndactyly Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Heart Defect, Tongue Hamartoma And Polysyndactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mucociliary Clearance Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mucociliary Clearance Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adrenocorticotropin Receptor Defect Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Adrenocorticotropin Receptor Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Color Vision Defect Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Color Vision Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Maturation Defect Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Maturation Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Restrictive Ventilatory Defect Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Restrictive Ventilatory Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Heart Defect (In Some Patients) Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Heart Defect (In Some Patients) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cardiac Conduction Defect Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cardiac Conduction Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Retinal Defect Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Glaucomatous Visual Field Defect Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Glaucomatous Visual Field Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Dynein Arm Defect Of Respiratory Motile Cilia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dynein Arm Defect Of Respiratory Motile Cilia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Generalized Hypotonia Due To Defect At The Neuromuscular Junction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Hypotonia Due To Defect At The Neuromuscular Junction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Iris Transillumination Defect Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Iris Transillumination Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Iodide Organification Defect Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Iodide Organification Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Electron Transfer Flavoprotein-Ubiquinone Oxidoreductase Defect Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Electron Transfer Flavoprotein-Ubiquinone Oxidoreductase Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cervical Segmentation Defect Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cervical Segmentation Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Lacrimal Duct Defect Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Lacrimal Duct Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Large Central Visual Field Defect Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Central Visual Field Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Unbalanced Atrioventricular Canal Defect Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Unbalanced Atrioventricular Canal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Afferent Pupillary Defect Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Afferent Pupillary Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Ventral Septal Defect Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ventral Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Thyroid Defect In Oxidation And Organification Of Iodide Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thyroid Defect In Oxidation And Organification Of Iodide in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Activating Thyroid-Stimulating Hormone Receptor Defect Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Activating Thyroid-Stimulating Hormone Receptor Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
perimembraneous ventricular septal defect Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the perimembraneous ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
ventricular septal defect Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
double outlet right ventricle with atrioventricular septal defect Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the double outlet right ventricle with atrioventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
atrial septal defect Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the atrial septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
atrioventricular septal defect Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the atrioventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
ostium secundum atrial septal defect Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the ostium secundum atrial septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
complete atrioventricular septal defect Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the complete atrioventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
muscular ventricular septal defect Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the muscular ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
ostium primum atrial septal defect Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the ostium primum atrial septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
inlet ventricular septal defect Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the inlet ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
aorticopulmonary septal defect Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the aorticopulmonary septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
iodide oxidation defect Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the iodide oxidation defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
partial atrioventricular septal defect Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the partial atrioventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
double outlet right ventricle, ventricular defect committed to aorta Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the double outlet right ventricle, ventricular defect committed to aorta phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
double outlet right ventricle, noncommitted ventricular septal defect Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the double outlet right ventricle, noncommitted ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
subarterial ventricular septal defect Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the subarterial ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
repair of mitotic kinetochore microtubule attachment defect Gene SetFrom GO Biological Process Annotations 2025 genes participating in the repair of mitotic kinetochore microtubule attachment defect biological process from the curated GO Biological Process Annotations 2025 dataset. |
Atrial heart septal defect Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Atrial heart septal defect from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Heart septal defect Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Heart septal defect from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Neural tube defect Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Neural tube defect from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Congenital bile acid synthesis defect Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital bile acid synthesis defect from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Congenital bile acid synthesis defect 2 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital bile acid synthesis defect 2 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Neural tube defect Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neural tube defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Heart septal defect Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Heart septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Ventricular septal defect Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ventricular septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Atrial heart septal defect Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrial heart septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Atrioventricular septal defect Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrioventricular septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital bile acid synthesis defect Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital bile acid synthesis defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital bile acid synthesis defect 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital bile acid synthesis defect 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Atrial heart septal defect 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrial heart septal defect 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Atrial heart septal defect 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrial heart septal defect 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Atrial heart septal defect 9 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrial heart septal defect 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Atrial heart septal defect 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrial heart septal defect 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Glycosylphosphatidylinositol biosynthesis defect 16 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Glycosylphosphatidylinositol biosynthesis defect 16 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Atrial heart septal defect 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrial heart septal defect 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Atrial heart septal defect 6 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrial heart septal defect 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Atrial heart septal defect 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrial heart septal defect 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Thrombophilia due to thrombin defect Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thrombophilia due to thrombin defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Qualitative platelet defect Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Qualitative platelet defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital bile acid synthesis defect 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital bile acid synthesis defect 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital bile acid synthesis defect 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital bile acid synthesis defect 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Joubert syndrome with orofaciodigital defect Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Joubert syndrome with orofaciodigital defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
X-linked thrombophilia due to factor IX defect Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked thrombophilia due to factor IX defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Atrial heart septal defect 8 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrial heart septal defect 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Developmental cardiac valvular defect Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental cardiac valvular defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital bile acid synthesis defect 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital bile acid synthesis defect 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
hypotrichosis-lymphedema-telangiectasia-renal defect syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease hypotrichosis-lymphedema-telangiectasia-renal defect syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Thrombophilia due to thrombomodulin defect Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thrombophilia due to thrombomodulin defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Nerve fibre bundle defect Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nerve fibre bundle defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Combined oxidative phosphorylation defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Combined oxidative phosphorylation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Thyroglobulin synthesis defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Thyroglobulin synthesis defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Iodotyrosine deiodination defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Iodotyrosine deiodination defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital defect of folate absorption Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital defect of folate absorption phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Neutral 1 amino acid transport defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Neutral 1 amino acid transport defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital bile acid synthesis defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital bile acid synthesis defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Atrioventricular septal defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Atrioventricular septal defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Thrombophilia due to thrombin defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Thrombophilia due to thrombin defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Iris transillumination defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Iris transillumination defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hepatoencephalopathy due to combined oxidative phosphorylation defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hepatoencephalopathy due to combined oxidative phosphorylation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Atrial septal defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Atrial septal defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Fatal mitochondrial disease due to combined oxidative phosphorylation defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Fatal mitochondrial disease due to combined oxidative phosphorylation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Renal carnitine transport defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Renal carnitine transport defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Ventricular septal defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Ventricular septal defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Glucose-6-phosphate transport defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Glucose-6-phosphate transport defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Phosphate transport defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Phosphate transport defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Peroxisome biogenesis disorder due to PEX1 defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Peroxisome biogenesis disorder due to PEX1 defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Laron- somatotropin defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Laron- somatotropin defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Color vision defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Color vision defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Protan defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Protan defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Iodotyrosyl coupling defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Iodotyrosyl coupling defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Neural tube defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Neural tube defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Gastrointestinal defect and immunodeficiency syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Gastrointestinal defect and immunodeficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Familial atrioventricular septal defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial atrioventricular septal defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Single Ventricle Defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Single Ventricle Defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Heart defect - tongue hamartoma - polysyndactyly syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Heart defect - tongue hamartoma - polysyndactyly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Metabolic myopathy due to lactate transporter defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Metabolic myopathy due to lactate transporter defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Methylmalonic acidemia due to transcobalamin receptor defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Methylmalonic acidemia due to transcobalamin receptor defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Sacral defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Sacral defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Bile acid conjugation defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Bile acid conjugation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Ulnar/fibula ray defect-brachydactyly syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Ulnar/fibula ray defect-brachydactyly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Immunodeficiency due to defect in CD3-gamma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Immunodeficiency due to defect in CD3-gamma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Thyroid Hormonogenesis Defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Thyroid Hormonogenesis Defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Oocyte maturation defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Oocyte maturation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Glycosylphosphatidylinositol biosynthesis defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycosylphosphatidylinositol biosynthesis defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
TRAF7-associated heart defect-digital anomalies-facial dysmorphism-motor and speech delay syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the TRAF7-associated heart defect-digital anomalies-facial dysmorphism-motor and speech delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Inherited oocyte maturation defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Inherited oocyte maturation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Atrioventricular septal defect and common atrioventricular junction Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Atrioventricular septal defect and common atrioventricular junction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Progressive retinal dystrophy due to retinol transport defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive retinal dystrophy due to retinol transport defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cardiac valvular defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cardiac valvular defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Juvenile arthritis due to defect in LA Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Juvenile arthritis due to defect in LA phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Female infertility due to zona pellucida defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Female infertility due to zona pellucida defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Left ventricular obstructive tract defect (inherited effect) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Left ventricular obstructive tract defect (inherited effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Left ventricular obstructive tract defect (maternal effect) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Left ventricular obstructive tract defect (maternal effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
furfuryl alcohol Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical furfuryl alcohol from the curated CTD Gene-Chemical Interactions dataset. |
3-methylbenzyl alcohol Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical 3-methylbenzyl alcohol from the curated CTD Gene-Chemical Interactions dataset. |
n-decyl alcohol Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical n-decyl alcohol from the curated CTD Gene-Chemical Interactions dataset. |
propargyl alcohol Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical propargyl alcohol from the curated CTD Gene-Chemical Interactions dataset. |
isobutyl alcohol Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical isobutyl alcohol from the curated CTD Gene-Chemical Interactions dataset. |
tert-Butyl Alcohol Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical tert-Butyl Alcohol from the curated CTD Gene-Chemical Interactions dataset. |
crotonyl alcohol Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical crotonyl alcohol from the curated CTD Gene-Chemical Interactions dataset. |
patchouli alcohol Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical patchouli alcohol from the curated CTD Gene-Chemical Interactions dataset. |
isopentyl alcohol Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical isopentyl alcohol from the curated CTD Gene-Chemical Interactions dataset. |
Benzyl Alcohol Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Benzyl Alcohol from the curated CTD Gene-Chemical Interactions dataset. |
2-(N-ethylperfluorooctanesulfonamido)ethyl alcohol Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical 2-(N-ethylperfluorooctanesulfonamido)ethyl alcohol from the curated CTD Gene-Chemical Interactions dataset. |
cinnamyl alcohol Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical cinnamyl alcohol from the curated CTD Gene-Chemical Interactions dataset. |
salicyl alcohol Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical salicyl alcohol from the curated CTD Gene-Chemical Interactions dataset. |
allyl alcohol Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical allyl alcohol from the curated CTD Gene-Chemical Interactions dataset. |
perilla alcohol Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical perilla alcohol from the curated CTD Gene-Chemical Interactions dataset. |
Alcohol-Induced Disorders, Nervous System Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alcohol-Induced Disorders, Nervous System from the curated CTD Gene-Disease Associations dataset. |
Fetal Alcohol Spectrum Disorders Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Fetal Alcohol Spectrum Disorders from the curated CTD Gene-Disease Associations dataset. |
ALCOHOL SENSITIVITY, ACUTE Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease ALCOHOL SENSITIVITY, ACUTE from the curated CTD Gene-Disease Associations dataset. |
Alcohol Withdrawal Seizures Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alcohol Withdrawal Seizures from the curated CTD Gene-Disease Associations dataset. |
Alcohol Drinking Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Alcohol Drinking in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
partial fetal alcohol syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease partial fetal alcohol syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
fetal alcohol syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fetal alcohol syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
fetal alcohol spectrum disorder Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fetal alcohol spectrum disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
alcohol abuse Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alcohol abuse in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
alcohol-induced mental disorder Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alcohol-induced mental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
alcohol dependence Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alcohol dependence in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
2,3,4,5,6-Pentafluorobenzyl Alcohol Gene Setinteracting proteins for the 2,3,4,5,6-Pentafluorobenzyl Alcohol drug from the curated DrugBank Drug Targets dataset. |
Para-Bromobenzyl Alcohol Gene Setinteracting proteins for the Para-Bromobenzyl Alcohol drug from the curated DrugBank Drug Targets dataset. |
2,4-Difluorobenzyl Alcohol 2,4-Difluoro-1-(Hydroxymethyl)Benzene Gene Setinteracting proteins for the 2,4-Difluorobenzyl Alcohol 2,4-Difluoro-1-(Hydroxymethyl)Benzene drug from the curated DrugBank Drug Targets dataset. |
2,3-Difluorobenzyl Alcohol Gene Setinteracting proteins for the 2,3-Difluorobenzyl Alcohol drug from the curated DrugBank Drug Targets dataset. |
Benzyl alcohol Gene Setinteracting proteins for the Benzyl alcohol drug from the curated DrugBank Drug Targets dataset. |
naltrexone response in alcohol-dependent patients Gene SetFrom GAD Gene-Disease Associations genes associated with the disease naltrexone response in alcohol-dependent patients in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol abuse; smoking behavior Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol abuse; smoking behavior in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol abuse; neuroticism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol abuse; neuroticism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
suicide, alcohol-dependent Gene SetFrom GAD Gene-Disease Associations genes associated with the disease suicide, alcohol-dependent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol amnestic disorder; alcoholism; alzheimer disease; alzheimer's disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol amnestic disorder; alcoholism; alzheimer disease; alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol drinking Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol drinking in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol abuse; drug dependence; affective psychoses Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol abuse; drug dependence; affective psychoses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depression; alcohol withdrawal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depression; alcohol withdrawal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol abuse; behavior problems Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol abuse; behavior problems in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol use Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol use in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol dependence; cocaine dependence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol dependence; cocaine dependence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol withdrawal seizures; alcoholism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol withdrawal seizures; alcoholism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol abuse; nicotine dependence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol abuse; nicotine dependence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol dependence; drug dependence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol dependence; drug dependence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol consumption Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol consumption in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol withdrawal seizures; alcoholism; disease models, animal; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol withdrawal seizures; alcoholism; disease models, animal; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol-induced disorders; esophageal neoplasms; liver cirrhosis, alcoholic; oesophageal neoplasm; pancreatitis, alcoholic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol-induced disorders; esophageal neoplasms; liver cirrhosis, alcoholic; oesophageal neoplasm; pancreatitis, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol abuse; cocaine abuse Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol abuse; cocaine abuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol-withdrawal delirium Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol-withdrawal delirium in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol withdrawl seizure and delirium tremens Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol withdrawl seizure and delirium tremens in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol dependency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol dependency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol dependence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol dependence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anxiety disorder; alcohol abuse Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anxiety disorder; alcohol abuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol associated symptoms; alcoholism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol associated symptoms; alcoholism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
schizophrenia; alcohol abuse; depressive disorder, major; dermal erythema; schizoaffective disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease schizophrenia; alcohol abuse; depressive disorder, major; dermal erythema; schizoaffective disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
parkinson's disease; alcohol abuse Gene SetFrom GAD Gene-Disease Associations genes associated with the disease parkinson's disease; alcohol abuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol abuse; impulse control disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol abuse; impulse control disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol abuse Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol abuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol-dependence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol-dependence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol dependence; alcoholic psychosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol dependence; alcoholic psychosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol-induced disorders, nervous system; alcoholism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol-induced disorders, nervous system; alcoholism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol-induced disorders; esophageal neoplasms; laryngeal neoplasms; oropharyngeal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol-induced disorders; esophageal neoplasms; laryngeal neoplasms; oropharyngeal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol effects Gene SetFrom 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. |
alcohol-induced disorders; prenatal exposure delayed effects Gene SetFrom 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. |
alcohol abuse; liver disease, alcoholic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol abuse; liver disease, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol-elimination rates Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol-elimination rates in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
delirium tremens, alcohol withdrawal-induced Gene SetFrom GAD Gene-Disease Associations genes associated with the disease delirium tremens, alcohol withdrawal-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
food and alcohol intake Gene SetFrom GAD Gene-Disease Associations genes associated with the disease food and alcohol intake in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol withdrawal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol withdrawal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol liver disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol liver disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcoholism; delirium tremens, alcohol-induced Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcoholism; delirium tremens, alcohol-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol withdrawal delirium; alcoholism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol withdrawal delirium; alcoholism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
severity of alcohol dependence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease severity of alcohol dependence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol dependence, panic disorder without agoraphobia, generalized anxiety disorder, narcolepsy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol dependence, panic disorder without agoraphobia, generalized anxiety disorder, narcolepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol withdrawal seizures; alcoholism; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol withdrawal seizures; alcoholism; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol elimination Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol elimination in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fetal alcohol syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fetal alcohol syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcoholism; alcohol withdrawal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcoholism; alcohol withdrawal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol abuse; blood pressure, arterial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol abuse; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term alcohol in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Alcohol poisoning_Pancreas_GSE3311 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Alcohol poisoning_Pancreas_GSE3311 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
alcohol catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the alcohol catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
primary alcohol metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the primary alcohol metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
alcohol metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the alcohol metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
primary alcohol catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the primary alcohol catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular alcohol metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular alcohol metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of response to alcohol Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of response to alcohol biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of response to alcohol Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of response to alcohol biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of response to alcohol Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of response to alcohol biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to alcohol Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to alcohol biological process from the curated GO Biological Process Annotations 2015 dataset. |
secondary alcohol metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the secondary alcohol metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
primary alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the primary alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
fatty alcohol metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the fatty alcohol metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular response to alcohol Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular response to alcohol biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
alcohol transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the alcohol transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
alcohol dehydrogenase [nad(p)+] activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the alcohol dehydrogenase [nad(p)+] activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
cdp-alcohol phosphatidyltransferase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the cdp-alcohol phosphatidyltransferase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
alcohol dehydrogenase activity, zinc-dependent Gene SetFrom GO Molecular Function Annotations 2015 genes performing the alcohol dehydrogenase activity, zinc-dependent molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
long-chain-alcohol oxidase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the long-chain-alcohol oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
long-chain-alcohol o-fatty-acyltransferase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the long-chain-alcohol o-fatty-acyltransferase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
alcohol dehydrogenase (nadp+) activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the alcohol dehydrogenase (nadp+) activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
alcohol sulfotransferase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the alcohol sulfotransferase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
fatty-acyl-coa reductase (alcohol-forming) activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the fatty-acyl-coa reductase (alcohol-forming) activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
phosphotransferase activity, alcohol group as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the phosphotransferase activity, alcohol group as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
alcohol binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the alcohol binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
alcohol dehydrogenase (nad) activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the alcohol dehydrogenase (nad) activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Alcoholism (alcohol dependence factor score) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Alcoholism (alcohol dependence factor score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Alcoholism (12-month weekly alcohol consumption) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Alcoholism (12-month weekly alcohol consumption) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Depression and alcohol dependence Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Depression and alcohol dependence phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Alcoholism (alcohol use disorder factor score) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Alcoholism (alcohol use disorder factor score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Diastolic blood pressure (alcohol consumption interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Diastolic blood pressure (alcohol consumption interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Alcohol consumption Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Alcohol consumption phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Alcohol dependence (age at onset) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Alcohol dependence (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Response to alcohol consumption (flushing response) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Response to alcohol consumption (flushing response) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Alcohol consumption (transferrin glycosylation) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Alcohol consumption (transferrin glycosylation) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Alcohol dependence Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Alcohol dependence phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Alcohol and nictotine co-dependence Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Alcohol and nictotine co-dependence phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Systolic blood pressure (alcohol consumption interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Systolic blood pressure (alcohol consumption interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Mean arterial pressure (alcohol consumption interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Mean arterial pressure (alcohol consumption interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Alcohol consumption (maxi-drinks) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Alcohol consumption (maxi-drinks) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Esophageal cancer (alcohol interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Esophageal cancer (alcohol interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
alcohol abuse Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease alcohol abuse in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
alcohol dependence Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease alcohol dependence in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
alcohol-induced mental disorder Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease alcohol-induced mental disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
Decyl alcohol Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Decyl alcohol metabolite from the curated HMDB Metabolites of Enzymes dataset. |
5-Hydroxyconiferyl alcohol Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the 5-Hydroxyconiferyl alcohol metabolite from the curated HMDB Metabolites of Enzymes dataset. |
4-Coumaryl alcohol Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the 4-Coumaryl alcohol metabolite from the curated HMDB Metabolites of Enzymes dataset. |
Propyl alcohol Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Propyl alcohol metabolite from the curated HMDB Metabolites of Enzymes dataset. |
Perillyl alcohol Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Perillyl alcohol metabolite from the curated HMDB Metabolites of Enzymes dataset. |
Coniferyl alcohol Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Coniferyl alcohol metabolite from the curated HMDB Metabolites of Enzymes dataset. |
Isopropyl alcohol Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Isopropyl alcohol metabolite from the curated HMDB Metabolites of Enzymes dataset. |
Sinapyl alcohol Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Sinapyl alcohol metabolite from the curated HMDB Metabolites of Enzymes dataset. |
Chlordecone alcohol Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Chlordecone alcohol metabolite from the curated HMDB Metabolites of Enzymes dataset. |
Arachidyl alcohol Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Arachidyl alcohol metabolite from the curated HMDB Metabolites of Enzymes dataset. |
facial flushing after alcohol intake Gene SetFrom HPO Gene-Disease Associations genes associated with the facial flushing after alcohol intake phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Alcohol-Induced Disorders, Nervous System Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Alcohol-Induced Disorders, Nervous System phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Alcohol-Induced Disorders Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Alcohol-Induced Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Alcohol Withdrawal Seizures Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Alcohol Withdrawal Seizures phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Fetal Alcohol Syndrome Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Fetal Alcohol Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Alcohol Amnestic Disorder Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Alcohol Amnestic Disorder phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Alcohol Withdrawal Delirium Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Alcohol Withdrawal Delirium phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Alcohol dehydrogenase, iron-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Alcohol dehydrogenase, iron-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Alcohol dehydrogenase family, zinc-type, class-V subfamily Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Alcohol dehydrogenase family, zinc-type, class-V subfamily protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Alcohol dehydrogenase, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Alcohol dehydrogenase, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Quinonprotein alcohol dehydrogenase-like superfamily Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Quinonprotein alcohol dehydrogenase-like superfamily protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Quinonprotein alcohol dehydrogenase-like domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Quinonprotein alcohol dehydrogenase-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Alcohol dehydrogenase class III/S-(hydroxymethyl)glutathione dehydrogenase Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Alcohol dehydrogenase class III/S-(hydroxymethyl)glutathione dehydrogenase protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Alcohol dehydrogenase family, zinc-type, class-IV subfamily Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Alcohol dehydrogenase family, zinc-type, class-IV subfamily protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vanillyl-alcohol oxidase, C-terminal subdomain 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vanillyl-alcohol oxidase, C-terminal subdomain 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Alcohol dehydrogenase superfamily, zinc-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Alcohol dehydrogenase superfamily, zinc-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Alcohol dehydrogenase GroES-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Alcohol dehydrogenase GroES-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
CDP-alcohol phosphatidyltransferase Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the CDP-alcohol phosphatidyltransferase protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Alcohol dehydrogenase, zinc-type, conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Alcohol dehydrogenase, zinc-type, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Alcohol dehydrogenase family, zinc-type, class-II subfamily Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Alcohol dehydrogenase family, zinc-type, class-II subfamily protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
enhanced behavioral response to alcohol Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the enhanced behavioral response to alcohol phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal alcohol consumption Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal alcohol consumption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased alcohol consumption Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased alcohol consumption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
alcohol preference Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the alcohol preference phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal behavioral response to alcohol Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal behavioral response to alcohol phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
impaired behavioral response to alcohol Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the impaired behavioral response to alcohol phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased alcohol consumption Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased alcohol consumption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
alcohol aversion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the alcohol aversion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
{alcohol dependence, protection against} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {alcohol dependence, protection against} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{alcohol dependence, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {alcohol dependence, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
alcohol sensitivity, acute Gene SetFrom OMIM Gene-Disease Associations genes associated with the alcohol sensitivity, acute phenotype from the curated OMIM Gene-Disease Associations dataset. |
{alcohol dependence} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {alcohol dependence} phenotype from the curated OMIM Gene-Disease Associations dataset. |
phosphotransferases-alcohol-group-acceptor Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term phosphotransferases-alcohol-group-acceptor in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
Folate-Alcohol and Cancer Pathway(Homo sapiens) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the Folate-Alcohol and Cancer Pathway(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset. |
Alcohol Or Other Drugs Use Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol Or Other Drugs Use in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alcohol Abuse Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol Abuse in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alcohol Use Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol Use Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alcohol Withdrawal Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol Withdrawal Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fetal Alcohol Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fetal Alcohol Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alcohol Abuse Or Dependence Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol Abuse Or Dependence in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fetus Or Newborn Affected By Alcohol Transmitted Via Placenta Or Breast Milk Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fetus Or Newborn Affected By Alcohol Transmitted Via Placenta Or Breast Milk in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alcohol-Induced Disorders, Nervous System Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol-Induced Disorders, Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ketoacidosis Due To Acute Alcohol Intoxication Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ketoacidosis Due To Acute Alcohol Intoxication in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alcohol Withdrawal Delirium Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol Withdrawal Delirium in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chlorpropamide-Alcohol Flushing Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chlorpropamide-Alcohol Flushing in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Partial Fetal Alcohol Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Partial Fetal Alcohol Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acute Alcohol Withdrawal Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acute Alcohol Withdrawal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alcohol Withdrawal Seizures Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol Withdrawal Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alcohol Toxicity Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol Toxicity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alcohol Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Alcohol Dependence Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Alcohol Dependence in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alcohol-Induced Chronic Pancreatitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol-Induced Chronic Pancreatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alcohol Dependence With Withdrawal, Unspecified Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol Dependence With Withdrawal, Unspecified in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Alcohol-Induced Mental Disorders Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Alcohol-Induced Mental Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Uncomplicated Alcohol Withdrawal Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Uncomplicated Alcohol Withdrawal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alcohol Consumption Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Alcohol Consumption in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hangover From Alcohol Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hangover From Alcohol in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hangover From Any Alcohol Or Other Drugs Substance Gene SetFrom 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. |
Alcohol Flush Reaction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Alcohol Flush Reaction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Alcohol Problem Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Alcohol Problem in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Response To Alcohol Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Response To Alcohol in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Alcohol Effect Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Alcohol Effect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Alcohol Sensitivity, Acute Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Alcohol Sensitivity, Acute in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Facial Flushing After Alcohol Intake Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Facial Flushing After Alcohol Intake in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Craving For Alcohol Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Craving For Alcohol in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Alcohol Dependence, Protection Against Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Alcohol Dependence, Protection Against in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Alcohol Sensitivity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Alcohol Sensitivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Prenatal Alcohol Exposure Gene SetFrom 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. |
Alcohol Consumption During Pregnancy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Alcohol Consumption During Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Alcohol Withdrawal-Induced Major Motor Seizure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Alcohol Withdrawal-Induced Major Motor Seizure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Status Epilepticus, Alcohol Withdrawal-Induced Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Status Epilepticus, Alcohol Withdrawal-Induced in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Alcohol Dependence, Susceptibility To Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Alcohol Dependence, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
alcohol catabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the alcohol catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
response to alcohol Gene SetFrom GO Biological Process Annotations 2023 genes participating in the response to alcohol biological process from the curated GO Biological Process Annotations 2023 dataset. |
secondary alcohol metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the secondary alcohol metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
secondary alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the secondary alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
cellular response to alcohol Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cellular response to alcohol biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
primary alcohol catabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the primary alcohol catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
primary alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the primary alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
tertiary alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the tertiary alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
primary alcohol metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the primary alcohol metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
fatty alcohol metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the fatty alcohol metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
tertiary alcohol metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the tertiary alcohol metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
alcohol dehydrogenase (NADP+) activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the alcohol dehydrogenase (NADP+) activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
phosphotransferase activity, alcohol group as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the phosphotransferase activity, alcohol group as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
alcohol dehydrogenase activity, zinc-dependent Gene SetFrom GO Molecular Function Annotations 2023 genes performing the alcohol dehydrogenase activity, zinc-dependent molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
alcohol dehydrogenase (NAD+) activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the alcohol dehydrogenase (NAD+) activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
long-chain-alcohol oxidase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the long-chain-alcohol oxidase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
alcohol sulfotransferase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the alcohol sulfotransferase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
long-chain-alcohol O-fatty-acyltransferase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the long-chain-alcohol O-fatty-acyltransferase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
alcohol-forming very long-chain fatty acyl-CoA reductase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the alcohol-forming very long-chain fatty acyl-CoA reductase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
alcohol dehydrogenase [NAD(P)+] activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the alcohol dehydrogenase [NAD(P)+] activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
CDP-alcohol phosphatidyltransferase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the CDP-alcohol phosphatidyltransferase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
alcohol transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the alcohol transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
enhanced behavioral response to alcohol Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the enhanced behavioral response to alcohol phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
alcohol preference Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the alcohol preference phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal alcohol consumption Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal alcohol consumption phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
impaired behavioral response to alcohol Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the impaired behavioral response to alcohol phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased alcohol consumption Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased alcohol consumption phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
alcohol aversion Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the alcohol aversion phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased alcohol consumption Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased alcohol consumption phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased susceptibility to alcohol-induced hepatic steatosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased susceptibility to alcohol-induced hepatic steatosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal behavioral response to alcohol Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal behavioral response to alcohol phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Coniferyl alcohol Gene SetFrom MW Enzyme Metabolite Associations interacting proteins for Coniferyl alcohol metabolite from the MW Gene Metabolite Associations dataset. |
Sinapyl alcohol Gene SetFrom MW Enzyme Metabolite Associations interacting proteins for Sinapyl alcohol metabolite from the MW Gene Metabolite Associations dataset. |
4-Coumaryl alcohol Gene SetFrom MW Enzyme Metabolite Associations interacting proteins for 4-Coumaryl alcohol metabolite from the MW Gene Metabolite Associations dataset. |
perillyl-alcohol Gene SetFrom LINCS L1000 CMAP Chemical Perturbation Consensus Signatures genes differentially expressed following the perillyl-alcohol small molecule perturbation from the LINCS L1000 CMAP Chemical Perturbation Consensus Signatures dataset. |
salicyl-alcohol Gene SetFrom LINCS L1000 CMAP Chemical Perturbation Consensus Signatures genes differentially expressed following the salicyl-alcohol small molecule perturbation from the LINCS L1000 CMAP Chemical Perturbation Consensus Signatures dataset. |
Folate alcohol and cancer pathway hypotheses Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Folate alcohol and cancer pathway hypotheses pathway from the WikiPathways Pathways 2024 dataset. |
alcohol metabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the alcohol metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
alcohol catabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the alcohol catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
response to alcohol Gene SetFrom GO Biological Process Annotations 2025 genes participating in the response to alcohol biological process from the curated GO Biological Process Annotations 2025 dataset. |
secondary alcohol metabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the secondary alcohol metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
secondary alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the secondary alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
cellular response to alcohol Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cellular response to alcohol biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
primary alcohol metabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the primary alcohol metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
tertiary alcohol metabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the tertiary alcohol metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
primary alcohol catabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the primary alcohol catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
primary alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the primary alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
tertiary alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the tertiary alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
fatty alcohol metabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the fatty alcohol metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
alcohol dehydrogenase (NADP+) activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the alcohol dehydrogenase (NADP+) activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
phosphotransferase activity, alcohol group as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the phosphotransferase activity, alcohol group as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
alcohol dehydrogenase (NAD+) activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the alcohol dehydrogenase (NAD+) activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
long-chain-alcohol oxidase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the long-chain-alcohol oxidase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
alcohol sulfotransferase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the alcohol sulfotransferase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
long-chain-alcohol O-fatty-acyltransferase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the long-chain-alcohol O-fatty-acyltransferase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
alcohol-forming long-chain fatty acyl-CoA reductase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the alcohol-forming long-chain fatty acyl-CoA reductase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
alcohol-forming very long-chain fatty acyl-CoA reductase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the alcohol-forming very long-chain fatty acyl-CoA reductase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
alcohol dehydrogenase [NAD(P)+] activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the alcohol dehydrogenase [NAD(P)+] activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
CDP-alcohol phosphatidyltransferase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the CDP-alcohol phosphatidyltransferase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Alcohol use disorder Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Alcohol use disorder from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Metabolic dysfunction and alcohol associated liver disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Metabolic dysfunction and alcohol associated liver disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Fetal alcohol spectrum disorder Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fetal alcohol spectrum disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Alcohol dependence Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Alcohol dependence in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Alcohol use disorder Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Alcohol use disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Fetal alcohol syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fetal alcohol syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
alcohol-induced mental disorder Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease alcohol-induced mental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Partial fetal alcohol syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Partial fetal alcohol syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Neurobehavioral disorder with prenatal alcohol exposure Gene SetFrom 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. |
Alcohol sensitivity Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Alcohol sensitivity phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Alcohol dependence Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Alcohol dependence phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Problematic alcohol use Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Problematic alcohol use phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol consumption Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol consumption phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol consumption (heavy vs. light/non-drinkers) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol consumption (heavy vs. light/non-drinkers) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol dependence Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol dependence phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Longitudinal alcohol consumption Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Longitudinal alcohol consumption phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol misuse (trauma interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol misuse (trauma interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Spine bone mineral density and alcohol drinking Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Spine bone mineral density and alcohol drinking phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Major depression and alcohol dependence Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Major depression and alcohol dependence phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Problematic alcohol use in trauma-exposed individuals Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Problematic alcohol use in trauma-exposed individuals phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol consumption over the past year Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol consumption over the past year phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol consumption in current drinkers Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol consumption in current drinkers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol consumption (drinks per week) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol consumption (drinks per week) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol consumption (drinkers vs non-drinkers) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol consumption (drinkers vs non-drinkers) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cleft lip with or without cleft palate x maternal periconceptional alcohol use interaction (parent of origin effect) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cleft lip with or without cleft palate x maternal periconceptional alcohol use interaction (parent of origin effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol use disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol use disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pulse pressure (alcohol consumption interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pulse pressure (alcohol consumption interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure (alcohol consumption interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure (alcohol consumption interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure (alcohol consumption interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure (alcohol consumption interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Mean arterial pressure (alcohol consumption interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mean arterial pressure (alcohol consumption interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol dependence (age at onset) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol dependence (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Fibrinogen levels (smoking status, alcohol consumption or body mass index interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Fibrinogen levels (smoking status, alcohol consumption or body mass index interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to alcohol consumption (flushing response) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to alcohol consumption (flushing response) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol consumption (max-drinks) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol consumption (max-drinks) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol and nicotine co-dependence Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol and nicotine co-dependence phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index (alcohol intake interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (alcohol intake interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Waist-to-hip circumference ratio (alcohol intake interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip circumference ratio (alcohol intake interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Depression and alcohol dependence Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Depression and alcohol dependence phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Initial alcohol sensitivity Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Initial alcohol sensitivity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol use disorder (dependence and problematic use scores) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol use disorder (dependence and problematic use scores) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol use disorder (total score) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol use disorder (total score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol use disorder (consumption score) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol use disorder (consumption score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcoholism (12-month weekly alcohol consumption) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcoholism (12-month weekly alcohol consumption) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcoholism (alcohol use disorder factor score) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcoholism (alcohol use disorder factor score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcoholism (alcohol dependence factor score) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcoholism (alcohol dependence factor score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Orofacial clefts (maternal alcohol consumption interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Orofacial clefts (maternal alcohol consumption interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol consumption (transferrin glycosylation) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol consumption (transferrin glycosylation) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Esophageal cancer (alcohol interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Esophageal cancer (alcohol interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Risky sexual behaviors (alcohol dependence interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Risky sexual behaviors (alcohol dependence interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Risky sexual behaviors in alcohol dependence Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Risky sexual behaviors in alcohol dependence phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol dependence symptom count Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol dependence symptom count phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Colorectal cancer (alcohol consumption interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Colorectal cancer (alcohol consumption interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cleft lip with or without cleft palate (maternal periconceptional alcohol intake interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cleft lip with or without cleft palate (maternal periconceptional alcohol intake interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure x alcohol consumption (light vs heavy) interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure x alcohol consumption (light vs heavy) interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure x alcohol consumption interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure x alcohol consumption interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure x alcohol consumption (light vs heavy) interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure x alcohol consumption (light vs heavy) interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pulse pressure x alcohol consumption interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pulse pressure x alcohol consumption interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Mean arterial pressure x alcohol consumption interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mean arterial pressure x alcohol consumption interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Mean arterial pressure x alcohol consumption (light vs heavy) interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mean arterial pressure x alcohol consumption (light vs heavy) interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pulse pressure x alcohol consumption (light vs heavy) interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pulse pressure x alcohol consumption (light vs heavy) interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol dependence (tolerance) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol dependence (tolerance) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol dependence (desire to cut drinking) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol dependence (desire to cut drinking) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol dependence (time spent drinking) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol dependence (time spent drinking) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Orofacial cleft x maternal periconceptional alcohol use interaction (1df) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Orofacial cleft x maternal periconceptional alcohol use interaction (1df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Orofacial cleft x maternal periconceptional alcohol use interaction (2df) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Orofacial cleft x maternal periconceptional alcohol use interaction (2df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Excessive alcohol consumption Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Excessive alcohol consumption phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure x alcohol consumption interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure x alcohol consumption interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
HDL cholesterol levels x alcohol consumption (drinkers vs non-drinkers) interaction (2df) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the HDL cholesterol levels x alcohol consumption (drinkers vs non-drinkers) interaction (2df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
LDL cholesterol levels x alcohol consumption (regular vs non-regular drinkers) interaction (2df) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the LDL cholesterol levels x alcohol consumption (regular vs non-regular drinkers) interaction (2df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol withdrawal symptoms Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol withdrawal symptoms phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Triglyceride levels x alcohol consumption (drinkers vs non-drinkers) interaction (2df) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Triglyceride levels x alcohol consumption (drinkers vs non-drinkers) interaction (2df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
LDL cholesterol levels x alcohol consumption (drinkers vs non-drinkers) interaction (2df) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the LDL cholesterol levels x alcohol consumption (drinkers vs non-drinkers) interaction (2df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Maximum habitual alcohol consumption Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Maximum habitual alcohol consumption phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
HDL cholesterol levels x alcohol consumption (regular vs non-regular drinkers) interaction (2df) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the HDL cholesterol levels x alcohol consumption (regular vs non-regular drinkers) interaction (2df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Triglyceride levels x alcohol consumption (regular vs non-regular drinkers) interaction (2df) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Triglyceride levels x alcohol consumption (regular vs non-regular drinkers) interaction (2df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Epigenetic age acceleration in alcohol use disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Epigenetic age acceleration in alcohol use disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol dependence or heroin dependence or methamphetamine dependence Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol dependence or heroin dependence or methamphetamine dependence phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol drinking status (current drinker vs non-current drinker) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol drinking status (current drinker vs non-current drinker) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
DEHYDRATED ALCOHOL Gene Setinteracting proteins for the DEHYDRATED ALCOHOL drug from theDGIdb Drug Targets 2026 dataset. |
PHENYLETHYL ALCOHOL Gene Setinteracting proteins for the PHENYLETHYL ALCOHOL drug from theDGIdb Drug Targets 2026 dataset. |
ISOPROPYL ALCOHOL Gene Setinteracting proteins for the ISOPROPYL ALCOHOL drug from theDGIdb Drug Targets 2026 dataset. |
LAURYL ALCOHOL DIPHOSPHONIC ACID Gene Setinteracting proteins for the LAURYL ALCOHOL DIPHOSPHONIC ACID drug from theDGIdb Drug Targets 2026 dataset. |
PERILLYL ALCOHOL Gene Setinteracting proteins for the PERILLYL ALCOHOL drug from theDGIdb Drug Targets 2026 dataset. |
METHYL ALCOHOL Gene Setinteracting proteins for the METHYL ALCOHOL drug from theDGIdb Drug Targets 2026 dataset. |
DICHLOROBENZYL ALCOHOL Gene Setinteracting proteins for the DICHLOROBENZYL ALCOHOL drug from theDGIdb Drug Targets 2026 dataset. |
Superior colliculus, motor related, intermediate white layer Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Superior colliculus, motor related, intermediate white layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Midbrain, sensory related Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Midbrain, sensory related relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Thalamus, polymodal association cortex related Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Thalamus, polymodal association cortex related relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Superior colliculus, motor related, deep white layer Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Superior colliculus, motor related, deep white layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Midbrain, behavioral state related Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Midbrain, behavioral state related relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Superior colliculus, sensory related Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Superior colliculus, sensory related relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Midbrain, motor related Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Midbrain, motor related relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Superior colliculus, motor related Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Superior colliculus, motor related relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Superior colliculus, motor related, deep gray layer Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Superior colliculus, motor related, deep gray layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Superior colliculus, motor related, intermediate gray layer, sublayer a Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Superior colliculus, motor related, intermediate gray layer, sublayer a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Superior colliculus, motor related, intermediate gray layer, sublayer c Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Superior colliculus, motor related, intermediate gray layer, sublayer c relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Superior colliculus, motor related, intermediate gray layer, sublayer b Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Superior colliculus, motor related, intermediate gray layer, sublayer b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Pons, motor related Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Pons, motor related relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Thalamus, sensory-motor cortex related Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Thalamus, sensory-motor cortex related relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Pons, behavioral state related Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Pons, behavioral state related relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Superior colliculus, motor related, intermediate gray layer Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Superior colliculus, motor related, intermediate gray layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Pons, sensory related Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Pons, sensory related relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Medulla, motor related Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Medulla, motor related relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Medulla, sensory related Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Medulla, sensory related relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
tnf/stress related signaling Gene SetFrom Biocarta Pathways proteins participating in the tnf/stress related signaling pathway from the Biocarta Pathways dataset. |
Myofibrillar myopathy, ZASP-related Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myofibrillar myopathy, ZASP-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
RRM2B-related mitochondrial disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the RRM2B-related mitochondrial disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thrombophilia, histidine-rich glycoprotein-related Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thrombophilia, histidine-rich glycoprotein-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pulmonary arterial hypertension related to hereditary hemorrhagic telangiectasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pulmonary arterial hypertension related to hereditary hemorrhagic telangiectasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Noonan syndrome and Noonan-related syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome and Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS, TARDBP-RELATED Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS, TARDBP-RELATED phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myofibrillar myopathy, filamin C-related Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myofibrillar myopathy, filamin C-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
FLNB-Related Disorders Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the FLNB-Related Disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
ZNF711-Related X-linked Mental Retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the ZNF711-Related X-linked Mental Retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
CEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the CEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NSDHL-Related Disorders Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NSDHL-Related Disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked mental retardation, with or without seizures, ARX-related Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation, with or without seizures, ARX-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Age-related macular degeneration 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Age-related macular degeneration 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Age-related macular degeneration 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Age-related macular degeneration 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
WFS1-Related Disorders Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the WFS1-Related Disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Age-related macular degeneration 11 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Age-related macular degeneration 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Age-related macular degeneration 14 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Age-related macular degeneration 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
GATA-1-related thrombocytopenia with dyserythropoiesis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the GATA-1-related thrombocytopenia with dyserythropoiesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
MACROTHROMBOCYTOPENIA, AUTOSOMAL DOMINANT, TUBB1-RELATED Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the MACROTHROMBOCYTOPENIA, AUTOSOMAL DOMINANT, TUBB1-RELATED phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
46,XY gonadal dysgenesis, complete, dhh-related Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the 46,XY gonadal dysgenesis, complete, dhh-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
AMYLOIDOSIS, LEPTOMENINGEAL, TRANSTHYRETIN-RELATED Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the AMYLOIDOSIS, LEPTOMENINGEAL, TRANSTHYRETIN-RELATED phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
CATSPER-Related Male Infertility Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the CATSPER-Related Male Infertility phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
MYH9 related disorders Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the MYH9 related disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
BLOC-3 (biogenesis of lysosome-related organelles complex 3) Gene Setproteins in the BLOC-3 (biogenesis of lysosome-related organelles complex 3) protein complex from the CORUM Protein Complexes dataset. |
BLOC-1 (biogenesis of lysosome-related organelles complex 1) Gene Setproteins in the BLOC-1 (biogenesis of lysosome-related organelles complex 1) protein complex from the CORUM Protein Complexes dataset. |
BLOC-2 (biogenesis of lysosome-related organelles complex 2) Gene Setproteins in the BLOC-2 (biogenesis of lysosome-related organelles complex 2) protein complex from the CORUM Protein Complexes dataset. |
SWI-SNF chromatin remodeling-related-BRCA1 complex Gene Setproteins in the SWI-SNF chromatin remodeling-related-BRCA1 complex protein complex from the CORUM Protein Complexes dataset. |
SWI/SNF-related complex Gene Setproteins in the SWI/SNF-related complex protein complex from the CORUM Protein Complexes dataset. |
myristoylated autocamtide-2-related inhibitory peptide Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical myristoylated autocamtide-2-related inhibitory peptide from the curated CTD Gene-Chemical Interactions dataset. |
calcitonin gene-related peptide (8-37) Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical calcitonin gene-related peptide (8-37) from the curated CTD Gene-Chemical Interactions dataset. |
Macular Degeneration, Age-Related, 11 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 11 from the curated CTD Gene-Disease Associations dataset. |
AIDS-Related Opportunistic Infections Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease AIDS-Related Opportunistic Infections from the curated CTD Gene-Disease Associations dataset. |
Macular Degeneration, Age-Related, 10 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 10 from the curated CTD Gene-Disease Associations dataset. |
Opioid-Related Disorders Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Opioid-Related Disorders from the curated CTD Gene-Disease Associations dataset. |
Glaucoma-Related Pigment Dispersion Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glaucoma-Related Pigment Dispersion Syndrome from the curated CTD Gene-Disease Associations dataset. |
Drug Metabolism, Poor, CYP2D6-Related Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Drug Metabolism, Poor, CYP2D6-Related from the curated CTD Gene-Disease Associations dataset. |
ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset. |
Drug Metabolism, Poor, CYP2C19-Related Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Drug Metabolism, Poor, CYP2C19-Related from the curated CTD Gene-Disease Associations dataset. |
AIDS-Related Complex Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease AIDS-Related Complex from the curated CTD Gene-Disease Associations dataset. |
NEVER IN MITOSIS GENE A-RELATED KINASE 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NEVER IN MITOSIS GENE A-RELATED KINASE 1 from the curated CTD Gene-Disease Associations dataset. |
Cerebral Amyloid Angiopathy, App-Related Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral Amyloid Angiopathy, App-Related from the curated CTD Gene-Disease Associations dataset. |
NOG-Related-Symphalangism Spectrum Disorder Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NOG-Related-Symphalangism Spectrum Disorder from the curated CTD Gene-Disease Associations dataset. |
CEREBELLAR DEGENERATION-RELATED AUTOANTIGEN 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease CEREBELLAR DEGENERATION-RELATED AUTOANTIGEN 3 from the curated CTD Gene-Disease Associations dataset. |
Amyloidosis, Hereditary, Transthyretin-Related Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Amyloidosis, Hereditary, Transthyretin-Related from the curated CTD Gene-Disease Associations dataset. |
Macular Degeneration, Age-Related, 9 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 9 from the curated CTD Gene-Disease Associations dataset. |
Macular Degeneration, Age-Related, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 3 from the curated CTD Gene-Disease Associations dataset. |
Macular Degeneration, Age-Related, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 2 from the curated CTD Gene-Disease Associations dataset. |
Macular Degeneration, Age-Related, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 1 from the curated CTD Gene-Disease Associations dataset. |
Macular Degeneration, Age-Related, 7 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 7 from the curated CTD Gene-Disease Associations dataset. |
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED from the curated CTD Gene-Disease Associations dataset. |
ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset. |
ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 7 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 7 from the curated CTD Gene-Disease Associations dataset. |
ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 5 from the curated CTD Gene-Disease Associations dataset. |
ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 8 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 8 from the curated CTD Gene-Disease Associations dataset. |
Mental Retardation, X-Linked, Syndromic, Jarid1c-Related Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic, Jarid1c-Related from the curated CTD Gene-Disease Associations dataset. |
Lymphoma, AIDS-Related Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lymphoma, AIDS-Related from the curated CTD Gene-Disease Associations dataset. |
AIDS-related Kaposi sarcoma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease AIDS-related Kaposi sarcoma from the curated CTD Gene-Disease Associations dataset. |
Cocaine-Related Disorders Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cocaine-Related Disorders from the curated CTD Gene-Disease Associations dataset. |
Substance-Related Disorders Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Substance-Related Disorders from the curated CTD Gene-Disease Associations dataset. |
46,XY Gonadal Dysgenesis, Complete or Partial, DHH-Related Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease 46,XY Gonadal Dysgenesis, Complete or Partial, DHH-Related from the curated CTD Gene-Disease Associations dataset. |
Cataract, Age-Related Cortical, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Age-Related Cortical, 1 from the curated CTD Gene-Disease Associations dataset. |
SCAPULOPERONEAL MYOPATHY, MYH7-RELATED Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease SCAPULOPERONEAL MYOPATHY, MYH7-RELATED from the curated CTD Gene-Disease Associations dataset. |
Macular Degeneration, Age-Related, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 4 from the curated CTD Gene-Disease Associations dataset. |
Macrothrombocytopenia, Autosomal Dominant, Tubb1-Related Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Macrothrombocytopenia, Autosomal Dominant, Tubb1-Related from the curated CTD Gene-Disease Associations dataset. |
Gout, HPRT-Related Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Gout, HPRT-Related from the curated CTD Gene-Disease Associations dataset. |
ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 4 from the curated CTD Gene-Disease Associations dataset. |
Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related from the curated CTD Gene-Disease Associations dataset. |
Age-Related Hearing Impairment 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Age-Related Hearing Impairment 1 from the curated CTD Gene-Disease Associations dataset. |
Cardiac Arrhythmia, Ankyrin-B-Related Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiac Arrhythmia, Ankyrin-B-Related from the curated CTD Gene-Disease Associations dataset. |
MYH9-Related Disorders Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MYH9-Related Disorders from the curated CTD Gene-Disease Associations dataset. |
Amphetamine-Related Disorders Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Amphetamine-Related Disorders from the curated CTD Gene-Disease Associations dataset. |
Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related from the curated CTD Gene-Disease Associations dataset. |
Myostatin-related muscle hypertrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myostatin-related muscle hypertrophy from the curated CTD Gene-Disease Associations dataset. |
Drug-Related Side Effects and Adverse Reactions Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Drug-Related Side Effects and Adverse Reactions from the curated CTD Gene-Disease Associations dataset. |
ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset. |
ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 6 from the curated CTD Gene-Disease Associations dataset. |
Muscular Dystrophy, Congenital, Lmna-Related Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, Lmna-Related from the curated CTD Gene-Disease Associations dataset. |
Substance-Related Disorders Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Substance-Related Disorders in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
sost-related sclerosing bone dysplasia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease sost-related sclerosing bone dysplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
age related macular degeneration Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease age related macular degeneration from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
substance-related disorder Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease substance-related disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
sost-related sclerosing bone dysplasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sost-related sclerosing bone dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |