Name

epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp phenotype from the curated OMIM Gene-Disease Associations dataset.

Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp from the curated CTD Gene-Disease Associations dataset.

writer's cramp Gene Set

From HPO Gene-Disease Associations

genes associated with the writer's cramp phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

exercise-induced muscle cramps Gene Set

From HPO Gene-Disease Associations

genes associated with the exercise-induced muscle cramps phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

epilepsy, absence; epilepsy, generalized; epilepsy, reflex; myoclonic epilepsy, juvenile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy, absence; epilepsy, generalized; epilepsy, reflex; myoclonic epilepsy, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

X-linked rolandic epilepsy with mental retardation and speech dyspraxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked rolandic epilepsy with mental retardation and speech dyspraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked from the curated CTD Gene-Disease Associations dataset.

?rolandic epilepsy, mental retardation, and speech dyspraxia Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?rolandic epilepsy, mental retardation, and speech dyspraxia phenotype from the curated OMIM Gene-Disease Associations dataset.

Epilepsy, Rolandic Gene Set

From CTD Gene-Disease Associations

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

Epilepsy, Rolandic Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Generalized epilepsy and paroxysmal dyskinesia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Generalized epilepsy and paroxysmal dyskinesia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Generalized Epilepsy and Paroxysmal Dyskinesia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Generalized Epilepsy and Paroxysmal Dyskinesia from the curated CTD Gene-Disease Associations dataset.

generalized epilepsy and paroxysmal dyskinesia Gene Set

From OMIM Gene-Disease Associations

genes associated with the generalized epilepsy and paroxysmal dyskinesia phenotype from the curated OMIM Gene-Disease Associations dataset.

Familial paroxysmal dystonia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial paroxysmal dystonia from the curated CTD Gene-Disease Associations dataset.

paroxysmal dystonia Gene Set

From HPO Gene-Disease Associations

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

cold-induced hand cramps Gene Set

From HPO Gene-Disease Associations

genes associated with the cold-induced hand cramps phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cold-induced muscle cramps Gene Set

From HPO Gene-Disease Associations

genes associated with the cold-induced muscle cramps phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Asthma, Exercise-Induced Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Asthma, Exercise-Induced from the curated CTD Gene-Disease Associations dataset.

asthma, exercise-induced Gene Set

From GAD Gene-Disease Associations

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

asthma, exercise-induced; bronchial hyperreactivity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma, exercise-induced; bronchial hyperreactivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

exercise-induced changes in insulin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease exercise-induced changes in insulin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

the extent of exercise-induced left ventricular growth in endurance athletes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease the extent of exercise-induced left ventricular growth in endurance athletes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

exercise-induced rhabdomyolysis Gene Set

From HPO Gene-Disease Associations

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

exercise-induced hemolysis Gene Set

From HPO Gene-Disease Associations

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

exercise-induced lactic acidemia Gene Set

From HPO Gene-Disease Associations

genes associated with the exercise-induced lactic acidemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

exercise-induced myalgia Gene Set

From HPO Gene-Disease Associations

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

exercise-induced myoglobinuria Gene Set

From HPO Gene-Disease Associations

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

exercise-induced muscle fatigue Gene Set

From HPO Gene-Disease Associations

genes associated with the exercise-induced muscle fatigue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

exercise-induced muscle stiffness Gene Set

From HPO Gene-Disease Associations

genes associated with the exercise-induced muscle stiffness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Asthma, Exercise-Induced Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Exercise-induced Circadian Regulation(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Exercise-induced Circadian Regulation(Mus musculus) pathway from the Wikipathways Pathways dataset.

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

From ClinVar Gene-Phenotype Associations

genes associated with the Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From CTD Gene-Disease Associations

genes/proteins associated with the disease Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps from the curated CTD Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

genes associated with the angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps phenotype from the curated OMIM Gene-Disease Associations dataset.

rolandic Gene Set

From GeneRIF Biological Term Annotations

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

akathisia, drug-induced; dystonia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease akathisia, drug-induced; dystonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Infantile convulsions and paroxysmal choreoathetosis, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile convulsions and paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

epilepsy; myoclonic epilepsy, juvenile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy; myoclonic epilepsy, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsy, absence; epilepsy, generalized Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy, absence; epilepsy, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsy, generalized; epilepsy, reflex Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy, generalized; epilepsy, reflex in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsy, generalized; epilepsy, tonic-clonic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy, generalized; epilepsy, tonic-clonic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Muscle Cramp Gene Set

From CTD Gene-Disease Associations

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

cramp Gene Set

From GeneRIF Biological Term Annotations

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

crampkenos Gene Set

From GeneRIF Biological Term Annotations

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

cramps Gene Set

From GeneRIF Biological Term Annotations

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

muscle cramps Gene Set

From HPO Gene-Disease Associations

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

Muscle Cramp Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

CRAMP1L Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for CRAMP1L from the Pathway Commons Protein-Protein Interactions dataset.

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

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, drug-induced; epilepsy; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced liver injury; epilepsy; hepatitis, toxic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; epilepsy; hepatitis, toxic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Death induced signaling complex DISC (FAS, FADD, CASP8, CFLAR), membrane-associated, CD95L induced Gene Set

From CORUM Protein Complexes

proteins in the Death induced signaling complex DISC (FAS, FADD, CASP8, CFLAR), membrane-associated, CD95L induced protein complex from the CORUM Protein Complexes dataset.

Death induced signaling complex II (FADD, CASP8, CFLAR), cytosolic, CD95L induced Gene Set

From CORUM Protein Complexes

proteins in the Death induced signaling complex II (FADD, CASP8, CFLAR), cytosolic, CD95L induced protein complex from the CORUM Protein Complexes dataset.

hypertension induced by pregnancy; hypertension, pregnancy-induced; pregnancy complications, hematologic; thrombophilia; venous thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension induced by pregnancy; hypertension, pregnancy-induced; pregnancy complications, hematologic; thrombophilia; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension induced by pregnancy; hypertension, pregnancy-induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension induced by pregnancy; hypertension, pregnancy-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal diseases; fetal growth retardation; hypertension induced by pregnancy; hypertension, pregnancy-induced; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal diseases; fetal growth retardation; hypertension induced by pregnancy; hypertension, pregnancy-induced; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension induced by pregnancy; hypertension, pregnancy-induced; pre-eclampsia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension induced by pregnancy; hypertension, pregnancy-induced; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

delirium tremens, alcohol withdrawal-induced; seizures, alcohol withdrawal-induced Gene Set

From 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.

Hypermanganesemia with dystonia, polycythemia and cirrhosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypermanganesemia with dystonia, polycythemia and cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY from the curated CTD Gene-Disease Associations dataset.

Hypermanganesemia with Dystonia Polycythemia and Cirrhosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypermanganesemia with Dystonia Polycythemia and Cirrhosis from the curated CTD Gene-Disease Associations dataset.

deafness, dystonia, and cerebral hypomyelination Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, dystonia, and cerebral hypomyelination phenotype from the curated OMIM Gene-Disease Associations dataset.

hypermanganesemia with dystonia, polycythemia, and cirrhosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypermanganesemia with dystonia, polycythemia, and cirrhosis phenotype from the curated OMIM Gene-Disease Associations dataset.

leukoencephalopathy with dystonia and motor neuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukoencephalopathy with dystonia and motor neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

Exercise Gene Set

From dbGAP Gene-Trait Associations

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

Exercise Test Gene Set

From dbGAP Gene-Trait Associations

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

exercise-mediated changes of insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease exercise-mediated changes of insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiorespiratory responses to exercise Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiorespiratory responses to exercise in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

impaired exercise stress response Gene Set

From GAD Gene-Disease Associations

genes associated with the disease impaired exercise stress response in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

exercise test Gene Set

From GAD Gene-Disease Associations

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

exercise efficiency Gene Set

From GAD Gene-Disease Associations

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

exercise (leisure time) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease exercise (leisure time) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; exercise Gene Set

From GAD Gene-Disease Associations

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

atrial natriuretic peptide activity after exercise Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial natriuretic peptide activity after exercise in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

exercise training Gene Set

From GAD Gene-Disease Associations

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

exercise Gene Set

From GAD Gene-Disease Associations

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

cardiac stroke volume to regular exercise Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiac stroke volume to regular exercise in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

exercise treadmill test traits Gene Set

From GAD Gene-Disease Associations

genes associated with the disease exercise treadmill test traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

exercise Gene Set

From GeneRIF Biological Term Annotations

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

Exercise treadmill test traits Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Exercise treadmill test traits phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Exercise (leisure time) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Exercise (leisure time) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

exercise intolerance Gene Set

From HPO Gene-Disease Associations

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

abnormal response to exercise Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal response to exercise phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal exercise endurance Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal exercise endurance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired exercise endurance Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired exercise endurance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

enhanced exercise endurance Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the enhanced exercise endurance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Paroxysmal atrial fibrillation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Paroxysmal atrial fibrillation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Paroxysmal nocturnal hemoglobinuria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Paroxysmal nocturnal hemoglobinuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Paroxysmal familial ventricular fibrillation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Paroxysmal familial ventricular fibrillation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ventricular fibrillation, paroxysmal familial, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ventricular fibrillation, paroxysmal familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Paroxysmal Extreme Pain Disorder Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Paroxysmal Extreme Pain Disorder from the curated CTD Gene-Disease Associations dataset.

Paroxysmal ventricular fibrillation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Paroxysmal ventricular fibrillation from the curated CTD Gene-Disease Associations dataset.

Paroxysmal nonkinesigenic dyskinesia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Paroxysmal nonkinesigenic dyskinesia from the curated CTD Gene-Disease Associations dataset.

Tachycardia, Paroxysmal Gene Set

From CTD Gene-Disease Associations

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

Hemoglobinuria, Paroxysmal Gene Set

From CTD Gene-Disease Associations

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

Paroxysmal Nonkinesigenic Dyskinesia 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Paroxysmal Nonkinesigenic Dyskinesia 2 from the curated CTD Gene-Disease Associations dataset.

Benign Paroxysmal Positional Vertigo Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Benign Paroxysmal Positional Vertigo from the curated CTD Gene-Disease Associations dataset.

benign paroxysmal positional nystagmus Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

anemia, aplastic; aplastic anemia; hemoglobinuria, paroxysmal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, aplastic; aplastic anemia; hemoglobinuria, paroxysmal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemoglobinuria, paroxysmal Gene Set

From GAD Gene-Disease Associations

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

paroxysmal Gene Set

From GeneRIF Biological Term Annotations

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

paroxysmal atrial fibrillation Gene Set

From HPO Gene-Disease Associations

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

paroxysmal choreoathetosis Gene Set

From HPO Gene-Disease Associations

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

paroxysmal ventricular tachycardia Gene Set

From HPO Gene-Disease Associations

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

paroxysmal atrial tachycardia Gene Set

From HPO Gene-Disease Associations

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

paroxysmal supraventricular tachycardia Gene Set

From HPO Gene-Disease Associations

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

paroxysmal lethargy Gene Set

From HPO Gene-Disease Associations

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

paroxysmal bursts of laughter Gene Set

From HPO Gene-Disease Associations

genes associated with the paroxysmal bursts of laughter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

paroxysmal involuntary eye movements Gene Set

From HPO Gene-Disease Associations

genes associated with the paroxysmal involuntary eye movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

paroxysmal drowsiness Gene Set

From HPO Gene-Disease Associations

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

paroxysmal dyskinesia Gene Set

From HPO Gene-Disease Associations

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

paroxysmal nocturnal hemoglobinuria Gene Set

From HPO Gene-Disease Associations

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

Hemoglobinuria, Paroxysmal Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

paroxysmal nonkinesigenic dyskinesia Gene Set

From OMIM Gene-Disease Associations

genes associated with the paroxysmal nonkinesigenic dyskinesia phenotype from the curated OMIM Gene-Disease Associations dataset.

paroxysmal extreme pain disorder, 167400, Gene Set

From OMIM Gene-Disease Associations

genes associated with the paroxysmal extreme pain disorder, 167400, phenotype from the curated OMIM Gene-Disease Associations dataset.

?paroxysmal nocturnal hemoglobinuria 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?paroxysmal nocturnal hemoglobinuria 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

ventricular fibrillation, paroxysmal familial, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ventricular fibrillation, paroxysmal familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

paroxysmal nonkinesigenic dyskinesia 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the paroxysmal nonkinesigenic dyskinesia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

paroxysmal nocturnal hemoglobinuria, somatic Gene Set

From OMIM Gene-Disease Associations

genes associated with the paroxysmal nocturnal hemoglobinuria, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.

convulsions, familial infantile, with paroxysmal choreoathetosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the convulsions, familial infantile, with paroxysmal choreoathetosis phenotype from the curated OMIM Gene-Disease Associations dataset.

Microcephaly, epilepsy, and diabetes syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, epilepsy, and diabetes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, X-linked, with variable learning disabilities and behavior disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Psychomotor retardation, epilepsy, and craniofacial dysmorphism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Psychomotor retardation, epilepsy, and craniofacial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders from the curated CTD Gene-Disease Associations dataset.

Hyperekplexia and Epilepsy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperekplexia and Epilepsy from the curated CTD Gene-Disease Associations dataset.

Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy from the curated CTD Gene-Disease Associations dataset.

epilepsy and mental retardation Gene Set

From GAD Gene-Disease Associations

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

polyhydramnios, megalencephaly, and symptomatic epilepsy Gene Set

From OMIM Gene-Disease Associations

genes associated with the polyhydramnios, megalencephaly, and symptomatic epilepsy phenotype from the curated OMIM Gene-Disease Associations dataset.

psychomotor retardation, epilepsy, and craniofacial dysmorphism Gene Set

From OMIM Gene-Disease Associations

genes associated with the psychomotor retardation, epilepsy, and craniofacial dysmorphism phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, x-linked, with variable learning disabilities and behavior disorders Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, x-linked, with variable learning disabilities and behavior disorders phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly, epilepsy, and diabetes syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, epilepsy, and diabetes syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, focal, with speech disorder and with or without mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, focal, with speech disorder and with or without mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, progressive myoclonic 1a (unverricht and lundborg) Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, progressive myoclonic 1a (unverricht and lundborg) phenotype from the curated OMIM Gene-Disease Associations dataset.

Acute urticaria and angioedema (non-steroidal anti-inflammatory drug-induced) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Acute urticaria and angioedema (non-steroidal anti-inflammatory drug-induced) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Sema4D induced cell migration and growth-cone collapse Gene Set

From Reactome Pathways

proteins participating in the Sema4D induced cell migration and growth-cone collapse pathway from the Reactome Pathways dataset.

Quercetin and Nf-kB/ AP-1 induced cell apoptosis(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Quercetin and Nf-kB/ AP-1 induced cell apoptosis(Homo sapiens) pathway from the Wikipathways Pathways dataset.

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

From Reactome Pathways

proteins participating in the Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways dataset.

Dystonia 24 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dystonia 24 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal dominant torsion dystonia 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal dominant torsion dystonia 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dystonia 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dystonia 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dystonia 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dystonia 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dystonia 16 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dystonia 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dystonia 18 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dystonia 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myoclonic dystonia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myoclonic dystonia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Juvenile-onset dystonia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Juvenile-onset dystonia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dystonia 25 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dystonia 25 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dystonia 6, torsion Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dystonia 6, torsion phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dystonia 5, Dopa-responsive type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dystonia 5, Dopa-responsive type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dystonia 3, torsion, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dystonia 3, torsion, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dystonia 1 Gene Set

From ClinVar Gene-Phenotype Associations

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

Infantile Parkinsonism-dystonia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile Parkinsonism-dystonia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinsonism-Dystonia, Infantile Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinsonism-Dystonia, Infantile from the curated CTD Gene-Disease Associations dataset.

Dystonia musculorum deformans type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dystonia musculorum deformans type 2 from the curated CTD Gene-Disease Associations dataset.

Dystonia 13, Torsion Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dystonia 13, Torsion from the curated CTD Gene-Disease Associations dataset.

Dystonia musculorum deformans type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dystonia musculorum deformans type 1 from the curated CTD Gene-Disease Associations dataset.

Torsion dystonia 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Torsion dystonia 7 from the curated CTD Gene-Disease Associations dataset.

Dystonia 17, Torsion, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dystonia 17, Torsion, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Dystonia 15, myoclonic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dystonia 15, myoclonic from the curated CTD Gene-Disease Associations dataset.

Dystonia 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dystonia 12 from the curated CTD Gene-Disease Associations dataset.

Myoclonic dystonia Gene Set

From CTD Gene-Disease Associations

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

Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency from the curated CTD Gene-Disease Associations dataset.

Juvenile-onset dystonia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Juvenile-onset dystonia from the curated CTD Gene-Disease Associations dataset.

Dystonia 3, Torsion, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dystonia 3, Torsion, X-Linked from the curated CTD Gene-Disease Associations dataset.

Dystonia 6, torsion Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dystonia 6, torsion from the curated CTD Gene-Disease Associations dataset.

Dystonia, Dopa-responsive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dystonia, Dopa-responsive from the curated CTD Gene-Disease Associations dataset.

Cervical Dystonia, Primary Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cervical Dystonia, Primary from the curated CTD Gene-Disease Associations dataset.

Dystonia Gene Set

From CTD Gene-Disease Associations

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

generalized dystonia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

dystonia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

deafness dystonia syndrome Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

dystonia Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

dystonia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cranio-facial dystonia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

focal dystonia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

generalized dystonia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

deafness dystonia syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

dystonia, primary torsion Gene Set

From GAD Gene-Disease Associations

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

complex regional pain syndromes; dystonia; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease complex regional pain syndromes; dystonia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myoclonus dystonia Gene Set

From GAD Gene-Disease Associations

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

dystonia; Gene Set

From GAD Gene-Disease Associations

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

idiopathic torsion dystonia Gene Set

From GAD Gene-Disease Associations

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

dystonia, primary Gene Set

From GAD Gene-Disease Associations

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

chromosome aberrations; chromosome deletion; dystonia; myoclonus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome deletion; dystonia; myoclonus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cervical dystonia Gene Set

From GAD Gene-Disease Associations

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

dystonia, cervical Gene Set

From GAD Gene-Disease Associations

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

dystonia, focal Gene Set

From GAD Gene-Disease Associations

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

blepharospasm; dystonia; dystonic disorders; torticollis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blepharospasm; dystonia; dystonic disorders; torticollis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dystonia Gene Set

From GAD Gene-Disease Associations

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

dystonia, early onset primary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dystonia, early onset primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dystonia; psychomotor disorders; syndrome Gene Set

From GAD Gene-Disease Associations

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

focal dystonia Gene Set

From GAD Gene-Disease Associations

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

dystonia Gene Set

From GeneRIF Biological Term Annotations

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

Musician's dystonia Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Musician's dystonia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

craniofacial dystonia Gene Set

From HPO Gene-Disease Associations

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

limb dystonia Gene Set

From HPO Gene-Disease Associations

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

generalized dystonia Gene Set

From HPO Gene-Disease Associations

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

axial dystonia Gene Set

From HPO Gene-Disease Associations

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

oromandibular dystonia Gene Set

From HPO Gene-Disease Associations

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

dystonia Gene Set

From HPO Gene-Disease Associations

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

laryngeal dystonia Gene Set

From HPO Gene-Disease Associations

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

torsion dystonia Gene Set

From HPO Gene-Disease Associations

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

focal dystonia Gene Set

From HPO Gene-Disease Associations

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

Dystonia Musculorum Deformans Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Dystonia Musculorum Deformans phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Dystonia Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

dystonia Gene Set

From MPO Gene-Phenotype Associations

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

dystonia 6, torsion Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia 6, torsion phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia-17, primary torsion Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia-17, primary torsion phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia-parkinsonism, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia-parkinsonism, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia 4, torsion, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia 4, torsion, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia 13, torsion Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia 13, torsion phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia-12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia-12 phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia 21 Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia 21 phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia 24 Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia 24 phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia 25 Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia 25 phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia, primary cervical Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia, primary cervical phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia, myoclonic Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia, myoclonic phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia-1, torsion Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia-1, torsion phenotype from the curated OMIM Gene-Disease Associations dataset.

{dystonia-1, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {dystonia-1, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

parkinsonism-dystonia, infantile Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinsonism-dystonia, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia-7, torsion Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia-7, torsion phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia-11, myoclonic Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia-11, myoclonic phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia, juvenile-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia, juvenile-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia-15, myoclonic Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia-15, myoclonic phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia 16 Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia 16 phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia, dopa-responsive, due to sepiapterin reductase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia, dopa-responsive, due to sepiapterin reductase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia, early-onset atypical, with myoclonic features Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia, early-onset atypical, with myoclonic features phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia, dopa-responsive, with or without hyperphenylalaninemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia, dopa-responsive, with or without hyperphenylalaninemia phenotype from the curated OMIM Gene-Disease Associations dataset.

Epilepsy, progressive myoclonic 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, progressive myoclonic 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epilepsy, progressive myoclonic 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, progressive myoclonic 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epilepsy, progressive myoclonic 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, progressive myoclonic 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epilepsy, partial, with variable foci Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, partial, with variable foci phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal dominant nocturnal frontal lobe epilepsy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal dominant nocturnal frontal lobe epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epilepsy, progressive myoclonic 4, with or without renal failure Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, progressive myoclonic 4, with or without renal failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epilepsy, nocturnal frontal lobe, 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, nocturnal frontal lobe, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Generalized epilepsy with febrile seizures plus 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Generalized epilepsy with febrile seizures plus 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pyridoxal 5'-phosphate-dependent epilepsy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pyridoxal 5'-phosphate-dependent epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amish infantile epilepsy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amish infantile epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epilepsy, progressive myoclonic 2b Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, progressive myoclonic 2b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Progressive myoclonus epilepsy with ataxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Progressive myoclonus epilepsy with ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Generalized epilepsy with febrile seizures plus, type 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Generalized epilepsy with febrile seizures plus, type 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Generalized epilepsy with febrile seizures plus, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Generalized epilepsy with febrile seizures plus, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Generalized epilepsy with febrile seizures plus, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Generalized epilepsy with febrile seizures plus, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Focal epilepsy with speech disorder with or without mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Focal epilepsy with speech disorder with or without mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epilepsy, lateral temporal lobe, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, lateral temporal lobe, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epilepsy, familial adult myoclonic, 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, familial adult myoclonic, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe myoclonic epilepsy in infancy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe myoclonic epilepsy in infancy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cortical dysplasia-focal epilepsy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cortical dysplasia-focal epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pyridoxine-dependent epilepsy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pyridoxine-dependent epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epilepsy, nocturnal frontal lobe, type 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, nocturnal frontal lobe, type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epilepsy, nocturnal frontal lobe, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, nocturnal frontal lobe, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epilepsy, nocturnal frontal lobe, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, nocturnal frontal lobe, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myoclonic epilepsy, familial infantile Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myoclonic epilepsy, familial infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epilepsy, Generalized Gene Set

From CTD Gene-Disease Associations

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

Generalized Epilepsy With Febrile Seizures Plus, Type 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Generalized Epilepsy With Febrile Seizures Plus, Type 6 from the curated CTD Gene-Disease Associations dataset.

Epilepsy, Frontal Lobe Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, Frontal Lobe from the curated CTD Gene-Disease Associations dataset.

EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS from the curated CTD Gene-Disease Associations dataset.

Epilepsy Gene Set

From CTD Gene-Disease Associations

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

Epilepsy, Idiopathic Generalized Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, Idiopathic Generalized from the curated CTD Gene-Disease Associations dataset.

Amish Infantile Epilepsy Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amish Infantile Epilepsy Syndrome from the curated CTD Gene-Disease Associations dataset.

Epilepsy, Female-Restricted, with Mental Retardation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, Female-Restricted, with Mental Retardation from the curated CTD Gene-Disease Associations dataset.

Cortical Dysplasia-Focal Epilepsy Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cortical Dysplasia-Focal Epilepsy Syndrome from the curated CTD Gene-Disease Associations dataset.

Epilepsy, Progressive Myoclonic, 1b Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, Progressive Myoclonic, 1b from the curated CTD Gene-Disease Associations dataset.

EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, with Epilepsy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, with Epilepsy from the curated CTD Gene-Disease Associations dataset.

Epilepsy, Tonic-Clonic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, Tonic-Clonic from the curated CTD Gene-Disease Associations dataset.

EPILEPSY, FAMILIAL TEMPORAL LOBE, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 3 from the curated CTD Gene-Disease Associations dataset.

EPILEPSY, FAMILIAL TEMPORAL LOBE, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 2 from the curated CTD Gene-Disease Associations dataset.

Epilepsy, Familial Adult Myoclonic, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, Familial Adult Myoclonic, 3 from the curated CTD Gene-Disease Associations dataset.

Generalized Epilepsy With Febrile Seizures Plus, Type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Generalized Epilepsy With Febrile Seizures Plus, Type 1 from the curated CTD Gene-Disease Associations dataset.

Generalized Epilepsy With Febrile Seizures Plus, Type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Generalized Epilepsy With Febrile Seizures Plus, Type 3 from the curated CTD Gene-Disease Associations dataset.

Generalized Epilepsy With Febrile Seizures Plus, Type 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Generalized Epilepsy With Febrile Seizures Plus, Type 4 from the curated CTD Gene-Disease Associations dataset.

Epilepsy, Temporal Lobe Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, Temporal Lobe from the curated CTD Gene-Disease Associations dataset.

Epilepsy, Partial, with Variable Foci Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, Partial, with Variable Foci from the curated CTD Gene-Disease Associations dataset.

EPILEPSY, HOT WATER, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPSY, HOT WATER, 1 from the curated CTD Gene-Disease Associations dataset.

Epilepsy, Benign Neonatal Gene Set

From CTD Gene-Disease Associations

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

EPILEPSY, FAMILIAL TEMPORAL LOBE, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 1 from the curated CTD Gene-Disease Associations dataset.

Epilepsy, Benign Neonatal, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, Benign Neonatal, 3 from the curated CTD Gene-Disease Associations dataset.

EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2 from the curated CTD Gene-Disease Associations dataset.

EPILEPSY, HOT WATER, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPSY, HOT WATER, 2 from the curated CTD Gene-Disease Associations dataset.

Epilepsy, Complex Partial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, Complex Partial from the curated CTD Gene-Disease Associations dataset.

Epilepsy, Myoclonic, Benign Adult Familial, Type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, Myoclonic, Benign Adult Familial, Type 1 from the curated CTD Gene-Disease Associations dataset.

Epilepsy, Absence Gene Set

From CTD Gene-Disease Associations

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

Epilepsy, Nocturnal Frontal Lobe, Type 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, Nocturnal Frontal Lobe, Type 4 from the curated CTD Gene-Disease Associations dataset.

Epilepsy, Nocturnal Frontal Lobe, Type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, Nocturnal Frontal Lobe, Type 2 from the curated CTD Gene-Disease Associations dataset.

Pyridoxine-dependent epilepsy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pyridoxine-dependent epilepsy from the curated CTD Gene-Disease Associations dataset.

Generalized Epilepsy With Febrile Seizures Plus, Type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Generalized Epilepsy With Febrile Seizures Plus, Type 2 from the curated CTD Gene-Disease Associations dataset.

Myoclonic Epilepsy, Juvenile Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myoclonic Epilepsy, Juvenile from the curated CTD Gene-Disease Associations dataset.

Epilepsy, Familial Temporal Lobe, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, Familial Temporal Lobe, 4 from the curated CTD Gene-Disease Associations dataset.

MYOCLONIC EPILEPSY, FAMILIAL INFANTILE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MYOCLONIC EPILEPSY, FAMILIAL INFANTILE from the curated CTD Gene-Disease Associations dataset.

Epilepsy, Nocturnal Frontal Lobe, Type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, Nocturnal Frontal Lobe, Type 3 from the curated CTD Gene-Disease Associations dataset.

Epilepsy, Nocturnal Frontal Lobe, Type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, Nocturnal Frontal Lobe, Type 1 from the curated CTD Gene-Disease Associations dataset.

Epilepsy, Partial, with Pericentral Spikes Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, Partial, with Pericentral Spikes from the curated CTD Gene-Disease Associations dataset.

Epilepsy Gene Set

From dbGAP Gene-Trait Associations

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

progressive myoclonus epilepsy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

juvenile myoclonic epilepsy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

epilepsy syndrome Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

epilepsy syndrome Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

juvenile absence epilepsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

benign familial infantile epilepsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

complex partial epilepsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

visual epilepsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

epilepsy syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

extratemporal epilepsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

epilepsy with generalized tonic-clonic seizures Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease epilepsy with generalized tonic-clonic seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

idiopathic generalized epilepsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

generalized epilepsy with febrile seizures plus Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease generalized epilepsy with febrile seizures plus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

temporal lobe epilepsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

benign epilepsy with centrotemporal spikes Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

benign familial neonatal epilepsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

partial motor epilepsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

progressive myoclonus epilepsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

childhood absence epilepsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

focal epilepsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

early onset absence epilepsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

epilepsy; fragile x syndrome Gene Set

From GAD Gene-Disease Associations

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

epilepsy; mental retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy; mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsy; anticoagulant complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy; anticoagulant complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug toxicity; epilepsy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug toxicity; epilepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsy Gene Set

From GAD Gene-Disease Associations

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

epilepsy; migraine disorders Gene Set

From GAD Gene-Disease Associations

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

myoclonic epilepsy, juvenile Gene Set

From GAD Gene-Disease Associations

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

epilepsy; malnutrition Gene Set

From GAD Gene-Disease Associations

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

epilepsy, temporal lobe; seizures, febrile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy, temporal lobe; seizures, febrile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug eruptions; drug hypersensitivity; epilepsy; stevens-johnson syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug eruptions; drug hypersensitivity; epilepsy; stevens-johnson syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsy; stevens-johnson syndrome; urticaria pigmentosa Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy; stevens-johnson syndrome; urticaria pigmentosa in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsy; rett syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy; rett syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsy, tonic-clonic Gene Set

From GAD Gene-Disease Associations

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

epilepsy, generalized Gene Set

From GAD Gene-Disease Associations

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

epilepsy, temporal lobe Gene Set

From GAD Gene-Disease Associations

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

epilepsy; recurrence Gene Set

From GAD Gene-Disease Associations

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

epilepsies, partial; epilepsy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsies, partial; epilepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsy, post-traumatic; seizures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy, post-traumatic; seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsy, temporal lobe; sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy, temporal lobe; sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

childhood absence epilepsy. Gene Set

From GAD Gene-Disease Associations

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

epilepsy, temporal lobe; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy, temporal lobe; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome deletion; epilepsy, generalized; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome deletion; epilepsy, generalized; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsy, temporal lobe; sclerosis; seizures, febrile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy, temporal lobe; sclerosis; seizures, febrile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug toxicity; epidermal necrolysis, toxic; epilepsy; stevens-johnson syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug toxicity; epidermal necrolysis, toxic; epilepsy; stevens-johnson syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

idiopathic epilepsy Gene Set

From GAD Gene-Disease Associations

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

epilepsy, temporal lobe; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy, temporal lobe; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

temporal lobe epilepsy Gene Set

From GAD Gene-Disease Associations

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

epilepsy, complex partial Gene Set

From GAD Gene-Disease Associations

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

juvenile myoclonic epilepsy Gene Set

From GAD Gene-Disease Associations

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

brain injuries; epilepsy, post-traumatic; seizures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain injuries; epilepsy, post-traumatic; seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cysts; epilepsy; tuberous sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cysts; epilepsy; tuberous sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsy; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

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

epilepsy; hyperhomocysteinemia; recurrence; substance withdrawal syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy; hyperhomocysteinemia; recurrence; substance withdrawal syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

confusion; epilepsy, temporal lobe; sclerosis; seizures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease confusion; epilepsy, temporal lobe; sclerosis; seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsy; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

epilepsy, generalized; seizures, febrile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy, generalized; seizures, febrile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsy; hyperammonemia Gene Set

From GAD Gene-Disease Associations

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

epilepsy, juvenile myoclonic Gene Set

From GAD Gene-Disease Associations

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

carbohydrate metabolism, inborn errors; dyskinesias; dyskinetic syndrome; epilepsy; mental retardation; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carbohydrate metabolism, inborn errors; dyskinesias; dyskinetic syndrome; epilepsy; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

nocturnal frontal lobe epilepsy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease nocturnal frontal lobe epilepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

confusion; epilepsy, temporal lobe Gene Set

From GAD Gene-Disease Associations

genes associated with the disease confusion; epilepsy, temporal lobe in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsy; neurotoxicity syndromes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy; neurotoxicity syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

generalized epilepsy Gene Set

From GAD Gene-Disease Associations

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

epilepsy; neurocysticercosis Gene Set

From GAD Gene-Disease Associations

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

epilepsy; Gene Set

From GAD Gene-Disease Associations

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

epilepsy, idiopathic generalized Gene Set

From GAD Gene-Disease Associations

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

epilepsy; seizures, febrile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy; seizures, febrile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrophy; epilepsy; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrophy; epilepsy; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsy, frontal lobe Gene Set

From GAD Gene-Disease Associations

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

epilepsies, partial; epilepsy, generalized; seizures, febrile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsies, partial; epilepsy, generalized; seizures, febrile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsy; seizures; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy; seizures; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsy; syndrome Gene Set

From GAD Gene-Disease Associations

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

epilepsy, frontal lobe; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy, frontal lobe; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

schizophrenia; epilepsy Gene Set

From GAD Gene-Disease Associations

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

epilepsy Gene Set

From GeneRIF Biological Term Annotations

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

Epilepsy (generalized) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Epilepsy (generalized) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Epilepsy Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Epilepsy (remission after treatment) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Epilepsy (remission after treatment) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

focal epilepsy Gene Set

From GWASdb SNP-Disease Associations

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

temporal lobe epilepsy Gene Set

From GWASdb SNP-Disease Associations

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

epilepsy syndrome Gene Set

From GWASdb SNP-Disease Associations

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

Epilepsy, Generalized Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Epilepsy, Frontal Lobe Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Epilepsy Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Epilepsy, Reflex Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Epilepsy, Tonic-Clonic Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Epilepsy, Post-Traumatic Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Epilepsy, Temporal Lobe Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Epilepsy, Benign Neonatal Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Epilepsy, Complex Partial Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Myoclonic Epilepsy, Juvenile Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Epilepsy, Absence Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

epilepsy, familial focal, with variable foci Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, familial focal, with variable foci phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, progressive myoclonic 3, with or without intracellular inclusions Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, progressive myoclonic 3, with or without intracellular inclusions phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, idiopathic generalized, susceptibility to, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, idiopathic generalized, susceptibility to, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, progressive myoclonic 2b (lafora) Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, progressive myoclonic 2b (lafora) phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, idiopathic generalized, 10} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, idiopathic generalized, 10} phenotype from the curated OMIM Gene-Disease Associations dataset.

centrotemporal epilepsy Gene Set

From OMIM Gene-Disease Associations

genes associated with the centrotemporal epilepsy phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, juvenile myoclonic, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, juvenile myoclonic, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, partial, with pericentral spikes Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, partial, with pericentral spikes phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, familial temporal lobe, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, familial temporal lobe, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, familial temporal lobe, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, familial temporal lobe, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, familial temporal lobe, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, familial temporal lobe, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, familial temporal lobe, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, familial temporal lobe, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, familial temporal lobe, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, familial temporal lobe, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy with progressive myoclonic epilepsy Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy with progressive myoclonic epilepsy phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, nocturnal frontal lobe, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, nocturnal frontal lobe, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, childhood absence, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, childhood absence, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, idiopathic generalized, susceptibility to, 9} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 9} phenotype from the curated OMIM Gene-Disease Associations dataset.

amish infantile epilepsy syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the amish infantile epilepsy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

{myoclonic epilepsy, juvenile, susceptibility to, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {myoclonic epilepsy, juvenile, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, idiopathic generalized, suscpetibility to, 12} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, idiopathic generalized, suscpetibility to, 12} phenotype from the curated OMIM Gene-Disease Associations dataset.

generalized epilepsy with febrile seizures plus, type 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the generalized epilepsy with febrile seizures plus, type 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

?epilepsy, familial adult myoclonic, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?epilepsy, familial adult myoclonic, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, generalized, with febrile seizures plus, type 5, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, generalized, with febrile seizures plus, type 5, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, juvenile myoclonic, susceptibility to, 5} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, juvenile myoclonic, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, childhood absence, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, childhood absence, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, idiopathic generalized, susceptibility to, 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, nocturnal frontal lobe, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, nocturnal frontal lobe, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, nocturnal frontal lobe, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, nocturnal frontal lobe, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

myoclonic epilepsy, juvenile, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the myoclonic epilepsy, juvenile, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, idiopathic generalized, susceptibility to 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, idiopathic generalized, susceptibility to 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, childhood absence, susceptibility to, 6} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, childhood absence, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, generalized, with febrile seizures plus, type 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, generalized, with febrile seizures plus, type 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, generalized, with febrile seizures plus, type 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, generalized, with febrile seizures plus, type 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, generalized, with febrile seizures plus, type 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, generalized, with febrile seizures plus, type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, generalized, with febrile seizures plus, type 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, generalized, with febrile seizures plus, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, generalized, with febrile seizures plus, type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, generalized, with febrile seizures plus, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, generalized, with febrile seizures plus, type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, generalized, with febrile seizures plus, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

cortical dysplasia-focal epilepsy syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the cortical dysplasia-focal epilepsy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, juvenile myoclonic, susceptiblity to, 9} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, juvenile myoclonic, susceptiblity to, 9} phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, childhood absence, susceptibility to, 4} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, childhood absence, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.

ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant Gene Set

From OMIM Gene-Disease Associations

genes associated with the ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, juvenile absence, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, juvenile absence, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, hot water, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, hot water, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, hot water, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, hot water, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, progressive myoclonic 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, progressive myoclonic 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, progressive myoclonic 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, progressive myoclonic 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, idiopathic generalized, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, idiopathic generalized, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, familial adult myoclonic, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, familial adult myoclonic, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, pyridoxine-dependent Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, pyridoxine-dependent phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, juvenile myoclonic, susceptibility to, 8} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, juvenile myoclonic, susceptibility to, 8} phenotype from the curated OMIM Gene-Disease Associations dataset.

myoclonic epilepsy, infantile, familial Gene Set

From OMIM Gene-Disease Associations

genes associated with the myoclonic epilepsy, infantile, familial phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, progressive myoclonic 4, with or without renal failure Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, progressive myoclonic 4, with or without renal failure phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, nocturnal frontal lobe, type 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, nocturnal frontal lobe, type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, nocturnal frontal lobe, type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, nocturnal frontal lobe, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, juvenile myoclonic, susceptibility to, 6} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, juvenile myoclonic, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, juvenile myoclonic 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, juvenile myoclonic 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, idiopathic generalized, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy idiopathic generalized, susceptibility to, 8} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy idiopathic generalized, susceptibility to, 8} phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, myoclonic, familial adult, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, myoclonic, familial adult, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, idiopathic generalized, susceptibility to, 6} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, childhood absence, susceptibility to, 5} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, childhood absence, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, idiopathic generalized, susceptibility to, 11} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 11} phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, juvenile absence, susceptibility to, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, juvenile absence, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, progressive myoclonic 1b Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, progressive myoclonic 1b phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, progressive myoclonic 2a (lafora) Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, progressive myoclonic 2a (lafora) phenotype from the curated OMIM Gene-Disease Associations dataset.

Myoclonic epilepsy of Lafora Gene Set

From Reactome Pathways

proteins participating in the Myoclonic epilepsy of Lafora pathway from the Reactome Pathways dataset.

double stranded rna induced gene expression Gene Set

From Biocarta Pathways

proteins participating in the double stranded rna induced gene expression pathway from the Biocarta Pathways dataset.

lectin induced complement pathway Gene Set

From Biocarta Pathways

proteins participating in the lectin induced complement pathway pathway from the Biocarta Pathways dataset.

cbl mediated ligand-induced downregulation of egf receptors pathway Gene Set

From Biocarta Pathways

proteins participating in the cbl mediated ligand-induced downregulation of egf receptors pathway pathway from the Biocarta Pathways dataset.

fmlp induced chemokine gene expression in hmc-1 cells Gene Set

From Biocarta Pathways

proteins participating in the fmlp induced chemokine gene expression in hmc-1 cells pathway from the Biocarta Pathways dataset.

bioactive peptide induced signaling pathway Gene Set

From Biocarta Pathways

proteins participating in the bioactive peptide induced signaling pathway pathway from the Biocarta Pathways dataset.

tsp-1 induced apoptosis in microvascular endothelial cell Gene Set

From Biocarta Pathways

proteins participating in the tsp-1 induced apoptosis in microvascular endothelial cell pathway from the Biocarta Pathways dataset.

oxidative stress induced gene expression via nrf2 Gene Set

From Biocarta Pathways

proteins participating in the oxidative stress induced gene expression via nrf2 pathway from the Biocarta Pathways dataset.

Cold-induced sweating syndrome 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cold-induced sweating syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

eNOS-HSP90-AKT complex, VEGF induced Gene Set

From CORUM Protein Complexes

proteins in the eNOS-HSP90-AKT complex, VEGF induced protein complex from the CORUM Protein Complexes dataset.

Bcl-xL-p53-PUMA complex, DNA damage induced Gene Set

From CORUM Protein Complexes

proteins in the Bcl-xL-p53-PUMA complex, DNA damage induced protein complex from the CORUM Protein Complexes dataset.

FAK-beta5 integrin complex, VEGF induced Gene Set

From CORUM Protein Complexes

proteins in the FAK-beta5 integrin complex, VEGF induced protein complex from the CORUM Protein Complexes dataset.

Ksr1-Mek-Braf-Erk complex, EGF induced Gene Set

From CORUM Protein Complexes

proteins in the Ksr1-Mek-Braf-Erk complex, EGF induced protein complex from the CORUM Protein Complexes dataset.

RAF1-RAS complex, EGF induced Gene Set

From CORUM Protein Complexes

proteins in the RAF1-RAS complex, EGF induced protein complex from the CORUM Protein Complexes dataset.

RNA-induced silencing complex, RISC Gene Set

From CORUM Protein Complexes

proteins in the RNA-induced silencing complex, RISC protein complex from the CORUM Protein Complexes dataset.

eNOS-HSP90 complex, VEGF induced Gene Set

From CORUM Protein Complexes

proteins in the eNOS-HSP90 complex, VEGF induced protein complex from the CORUM Protein Complexes dataset.

CRMP-MICAL-PlexinA1 complex, induced by SEMA3A Gene Set

From CORUM Protein Complexes

proteins in the CRMP-MICAL-PlexinA1 complex, induced by SEMA3A protein complex from the CORUM Protein Complexes dataset.

Wave1-Bcl-xl-Pancortin-2 complex, focal ischemic stroke induced Gene Set

From CORUM Protein Complexes

proteins in the Wave1-Bcl-xl-Pancortin-2 complex, focal ischemic stroke induced protein complex from the CORUM Protein Complexes dataset.

Ask1-Traf6 complex, LPS induced Gene Set

From CORUM Protein Complexes

proteins in the Ask1-Traf6 complex, LPS induced protein complex from the CORUM Protein Complexes dataset.

Ksr1-Mek-Braf complex, EGF induced Gene Set

From CORUM Protein Complexes

proteins in the Ksr1-Mek-Braf complex, EGF induced protein complex from the CORUM Protein Complexes dataset.

p53-Bcl-xL complex, DNA-damage induced Gene Set

From CORUM Protein Complexes

proteins in the p53-Bcl-xL complex, DNA-damage induced protein complex from the CORUM Protein Complexes dataset.

PUMA-Bcl-xL complex, DNA-damage induced Gene Set

From CORUM Protein Complexes

proteins in the PUMA-Bcl-xL complex, DNA-damage induced protein complex from the CORUM Protein Complexes dataset.

Neoplasms, Radiation-Induced Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neoplasms, Radiation-Induced from the curated CTD Gene-Disease Associations dataset.

Cold-Induced Sweating Syndrome 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cold-Induced Sweating Syndrome 1 from the curated CTD Gene-Disease Associations dataset.

Dyskinesia, Drug-Induced Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dyskinesia, Drug-Induced from the curated CTD Gene-Disease Associations dataset.

HEARING LOSS, CISPLATIN-INDUCED, SUSCEPTIBILITY TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEARING LOSS, CISPLATIN-INDUCED, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.

Alcohol-Induced Disorders, Nervous System Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alcohol-Induced Disorders, Nervous System from the curated CTD Gene-Disease Associations dataset.

Drug-Induced Liver Injury, Chronic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Drug-Induced Liver Injury, Chronic from the curated CTD Gene-Disease Associations dataset.

Deafness, Aminoglycoside-Induced Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, Aminoglycoside-Induced from the curated CTD Gene-Disease Associations dataset.

ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.

Radiation induced meningioma Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Radiation induced meningioma from the curated CTD Gene-Disease Associations dataset.

Drug-Induced Liver Injury Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Drug-Induced Liver Injury from the curated CTD Gene-Disease Associations dataset.

Asthma, Aspirin-Induced Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Asthma, Aspirin-Induced from the curated CTD Gene-Disease Associations dataset.

Psychoses, Substance-Induced Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Psychoses, Substance-Induced from the curated CTD Gene-Disease Associations dataset.

Hypertension, Pregnancy-Induced Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypertension, Pregnancy-Induced from the curated CTD Gene-Disease Associations dataset.

Hypoglycemia, leucine-induced Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypoglycemia, leucine-induced from the curated CTD Gene-Disease Associations dataset.

Hearing Loss, Noise-Induced Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hearing Loss, Noise-Induced from the curated CTD Gene-Disease Associations dataset.

Abnormalities, Drug-Induced Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Abnormalities, Drug-Induced from the curated CTD Gene-Disease Associations dataset.

Akathisia, Drug-Induced Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Akathisia, Drug-Induced from the curated CTD Gene-Disease Associations dataset.

Drug-Induced Liver Injury Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Drug-Induced Liver Injury in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

drug-induced hepatitis Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

drug-induced hepatitis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

substance-induced psychosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

alcohol-induced mental disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation 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.

drug-induced mental disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

steroid-induced glaucoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

tpa-induced apoptosis Gene Set

From GAD Gene-Disease Associations

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

drug-induced liver injury; hematologic diseases; hepatitis, toxic; large-cell lymphomas; lymphoma, large b-cell, diffuse; mucositis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; hematologic diseases; hepatitis, toxic; large-cell lymphomas; lymphoma, large b-cell, diffuse; mucositis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenosine diphosphate-induced platelet aggregation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenosine diphosphate-induced platelet aggregation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced liver injury; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; cocarcinogenesis; neoplasms, radiation-induced; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; cocarcinogenesis; neoplasms, radiation-induced; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dyskinesia, drug-induced Gene Set

From GAD Gene-Disease Associations

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

preeclampsia; hypertension, pregnancy induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease preeclampsia; hypertension, pregnancy induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

risperidone-induced extrapyramidal symptoms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease risperidone-induced extrapyramidal symptoms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

erythropoietin induced hypertension Gene Set

From GAD Gene-Disease Associations

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

eclampsia; hypertension, pregnancy-induced; pre-eclampsia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eclampsia; hypertension, pregnancy-induced; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced liver injury, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dyskinesia, drug-induced; movement disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dyskinesia, drug-induced; movement disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, papillary; lymphatic metastasis; neoplasms, radiation-induced; thyroid neoplasm; thyroid neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, papillary; lymphatic metastasis; neoplasms, radiation-induced; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neoplasms, radiation-induced; thyroid neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neoplasms, radiation-induced; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma, aspirin-induced; urticaria, aspirin-intolerant Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma, aspirin-induced; urticaria, aspirin-intolerant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

psychoses, substance-induced; substance-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease psychoses, substance-induced; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

phenytoin-induced congenital malformations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease phenytoin-induced congenital malformations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lupus erythematosus; nephrotic syndrome; agranulocytosis, drug induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lupus erythematosus; nephrotic syndrome; agranulocytosis, drug induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chemotherapy-induced pulmonary fibrosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chemotherapy-induced pulmonary fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

akathisia, drug-induced; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease akathisia, drug-induced; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

antipsychotic-induced adverse reactions Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antipsychotic-induced adverse reactions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy-induced chylomicronemia Gene Set

From GAD Gene-Disease Associations

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

bipolar disorder; mania, antidepressant-induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bipolar disorder; mania, antidepressant-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced liver injury (flucloxacillin) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury (flucloxacillin) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

basal ganglia diseases; dyskinesia, drug-induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease basal ganglia diseases; dyskinesia, drug-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension, pregnancy-induced; pre-eclampsia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension, pregnancy-induced; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma (toluene diisocyanate-induced) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma (toluene diisocyanate-induced) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, papillary; dna damage; neoplasms, radiation-induced; thyroid neoplasm; thyroid neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, papillary; dna damage; neoplasms, radiation-induced; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

agitation; dyskinesia, drug-induced; psychomotor agitation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease agitation; dyskinesia, drug-induced; psychomotor agitation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

weight gain (antipsychotic-drug induced) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease weight gain (antipsychotic-drug induced) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced liver injury; graft vs host disease; inflammation; leukemia; liver diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; graft vs host disease; inflammation; leukemia; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

radiation-induced ocular telangiectasia Gene Set

From GAD Gene-Disease Associations

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

amphetamine-related disorders; psychoses, substance-induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amphetamine-related disorders; psychoses, substance-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heparin-induced thrombocytopenia Gene Set

From GAD Gene-Disease Associations

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

caffeine-induced anxiety. Gene Set

From GAD Gene-Disease Associations

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

hdac inhibitor-induced growth arrest. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hdac inhibitor-induced growth arrest. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced long-qt syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced long-qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcohol-induced disorders; esophageal neoplasms; liver cirrhosis, alcoholic; oesophageal neoplasm; pancreatitis, alcoholic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcohol-induced disorders; esophageal neoplasms; liver cirrhosis, alcoholic; oesophageal neoplasm; pancreatitis, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension, pregnancy-induced; pre-eclampsia; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension, pregnancy-induced; pre-eclampsia; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

antipsychotic agent-induced weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antipsychotic agent-induced weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced liver injury; latent tuberculosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; latent tuberculosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neoplasms, radiation-induced; occupational diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neoplasms, radiation-induced; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiotoxicity, anthracycline-induced Gene Set

From GAD Gene-Disease Associations

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

marijuana abuse; psychoses, substance-induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease marijuana abuse; psychoses, substance-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

antibiotic-induced cutaneous allergic reactions Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antibiotic-induced cutaneous allergic reactions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dyskinesias, levodopa-induced Gene Set

From GAD Gene-Disease Associations

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

methamphetamine induced psychosis Gene Set

From GAD Gene-Disease Associations

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

gingival overgrowth, drug induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gingival overgrowth, drug induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

nevirapine-induced rash-hiv Gene Set

From GAD Gene-Disease Associations

genes associated with the disease nevirapine-induced rash-hiv in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced liver injury; gastrointestinal diseases; psoriasis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; gastrointestinal diseases; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anticholinergic challenge-induced memory impairment Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anticholinergic challenge-induced memory impairment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced liver injury; hepatitis, toxic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; hepatitis, toxic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced liver injury Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

preeclampsia; hypertension, pregnancy induced; eclampsia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease preeclampsia; hypertension, pregnancy induced; eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mania, antidepressant-induced Gene Set

From GAD Gene-Disease Associations

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

arsenic-induced hyperkeratosis Gene Set

From GAD Gene-Disease Associations

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

morphine-induced adverse drug reactions Gene Set

From GAD Gene-Disease Associations

genes associated with the disease morphine-induced adverse drug reactions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced liver injury; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

helicobacter pylori infection; gastritis, helicobacter pylori-induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease helicobacter pylori infection; gastritis, helicobacter pylori-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

inflammatory response, trauma induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease inflammatory response, trauma induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

akathisia, drug-induced Gene Set

From GAD Gene-Disease Associations

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

hodgkin disease; neoplasms, radiation-induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hodgkin disease; neoplasms, radiation-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

agranulocytosis, drug induced Gene Set

From GAD Gene-Disease Associations

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

drug-induced liver injury; liver diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced liver injury; hepatitis, toxic; tuberculosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; hepatitis, toxic; tuberculosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced liver injury; liver diseases; tuberculosis, pulmonary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; liver diseases; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing impairment; hearing loss; hearing loss, noise-induced; occupational diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing impairment; hearing loss; hearing loss, noise-induced; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dyskinesia, drug-induced; parkinsonian disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dyskinesia, drug-induced; parkinsonian disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, papillary; neoplasms, radiation-induced; thyroid neoplasm; thyroid neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, papillary; neoplasms, radiation-induced; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcohol-induced disorders, nervous system; alcoholism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcohol-induced disorders, nervous system; alcoholism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcohol-induced disorders; esophageal neoplasms; laryngeal neoplasms; oropharyngeal neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcohol-induced disorders; esophageal neoplasms; laryngeal neoplasms; oropharyngeal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced liver injury; tuberculosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; tuberculosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fluvastatin induced cholesterol changes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fluvastatin induced cholesterol changes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lupus erythematosus; agranulocytosis, drug induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lupus erythematosus; agranulocytosis, drug induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcohol-induced disorders; prenatal exposure delayed effects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcohol-induced disorders; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

delirium tremens, alcohol withdrawal-induced Gene Set

From 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.

hypertension, pregnancy-induced Gene Set

From GAD Gene-Disease Associations

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

drug-induced liver injury; hematologic diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; hematologic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aspirin-induced asthma Gene Set

From GAD Gene-Disease Associations

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

pollen-induced allergic rhinitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pollen-induced allergic rhinitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neoplasms, radiation-induced; thyroid neoplasm; thyroid neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neoplasms, radiation-induced; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, noise-induced; occupational diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, noise-induced; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcoholism; delirium tremens, alcohol-induced Gene Set

From 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.

hearing loss, noise-induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, noise-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension, pregnancy-induced; proteinuria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension, pregnancy-induced; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

radiation-induced damage to normal tissues Gene Set

From GAD Gene-Disease Associations

genes associated with the disease radiation-induced damage to normal tissues in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hcv-induced liver fibrosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hcv-induced liver fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

delirium tremens, alcohol-induced; alcohol withdrawal Gene Set

From 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.

carcinoma, basal cell; carcinoma, squamous cell; neoplasms, radiation-induced; skin neoplasms; sunburn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; neoplasms, radiation-induced; skin neoplasms; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

clozapine-induced agranulocytosis Gene Set

From GAD Gene-Disease Associations

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

weight gain, antipsychotic drug-induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease weight gain, antipsychotic drug-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dyskinesia, drug-induced; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dyskinesia, drug-induced; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, drug-induced; cleft lip; cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, drug-induced; cleft lip; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chemotherapy-induced leukemia Gene Set

From GAD Gene-Disease Associations

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

drug-induced liver injury; hepatitis, toxic; tuberculosis, pulmonary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; hepatitis, toxic; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension, pregnancy induced Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease; drug-induced liver injury; liver diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; drug-induced liver injury; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced liver injury; tuberculosis, pulmonary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brill-symmers disease; lymphoma, follicular; lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; neoplasms, radiation-induced; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brill-symmers disease; lymphoma, follicular; lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; neoplasms, radiation-induced; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced liver injury; liver failure, acute Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; liver failure, acute in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dyskinesia, drug-induced; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dyskinesia, drug-induced; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

psychoses, substance-induced Gene Set

From GAD Gene-Disease Associations

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

induced Gene Set

From GeneRIF Biological Term Annotations

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

E2F3_KD_GDS4094_448_mouse_Mammary tumors (Myc-induced) Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the E2F3_KD_GDS4094_448_mouse_Mammary tumors (Myc-induced) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

TGM2_KD_GSE23702_716_human_NB4 cells, 72h ATRA-induced differentiation Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the TGM2_KD_GSE23702_716_human_NB4 cells, 72h ATRA-induced differentiation gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

E2F2_KD_GDS4094_447_mouse_Mammary tumors (Myc-induced) Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the E2F2_KD_GDS4094_447_mouse_Mammary tumors (Myc-induced) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

negative regulation of oxidative stress-induced cell death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations dataset.

regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

histamine-induced gastric acid secretion Gene Set

From GO Biological Process Annotations

genes participating in the histamine-induced gastric acid secretion biological process from the curated GO Biological Process Annotations dataset.

regulation of viral-induced cytoplasmic pattern recognition receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of viral-induced cytoplasmic pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of oxidative stress-induced intrinsic apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of oxidative stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

activation-induced cell death of t cells Gene Set

From GO Biological Process Annotations

genes participating in the activation-induced cell death of t cells biological process from the curated GO Biological Process Annotations dataset.

gastrin-induced gastric acid secretion Gene Set

From GO Biological Process Annotations

genes participating in the gastrin-induced gastric acid secretion biological process from the curated GO Biological Process Annotations dataset.

regulation of hypoxia-induced intrinsic apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of hypoxia-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

mitochondrion degradation by induced vacuole formation Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrion degradation by induced vacuole formation biological process from the curated GO Biological Process Annotations dataset.

negative regulation of viral-induced cytoplasmic pattern recognition receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of viral-induced cytoplasmic pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

dna damage induced protein phosphorylation Gene Set

From GO Biological Process Annotations

genes participating in the dna damage induced protein phosphorylation biological process from the curated GO Biological Process Annotations dataset.

positive regulation of oxidative stress-induced neuron death Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of oxidative stress-induced neuron death biological process from the curated GO Biological Process Annotations dataset.

positive regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of oxidative stress-induced intrinsic apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of oxidative stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

negative regulation of hydrogen peroxide-induced neuron intrinsic apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of hydrogen peroxide-induced neuron intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of oxidative stress-induced cell death Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations dataset.

negative regulation of oxidative stress-induced neuron death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of oxidative stress-induced neuron death biological process from the curated GO Biological Process Annotations dataset.

negative regulation of hydrogen peroxide-induced cell death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of hydrogen peroxide-induced cell death biological process from the curated GO Biological Process Annotations dataset.

negative regulation of activation-induced cell death of t cells Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of activation-induced cell death of t cells biological process from the curated GO Biological Process Annotations dataset.

oncogene-induced cell senescence Gene Set

From GO Biological Process Annotations

genes participating in the oncogene-induced cell senescence biological process from the curated GO Biological Process Annotations dataset.

regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

negative regulation of oxidative stress-induced intrinsic apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of oxidative stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

diet induced thermogenesis Gene Set

From GO Biological Process Annotations

genes participating in the diet induced thermogenesis biological process from the curated GO Biological Process Annotations dataset.

negative regulation of hypoxia-induced intrinsic apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of hypoxia-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

stress-induced mitochondrial fusion Gene Set

From GO Biological Process Annotations

genes participating in the stress-induced mitochondrial fusion biological process from the curated GO Biological Process Annotations dataset.

stress-induced premature senescence Gene Set

From GO Biological Process Annotations

genes participating in the stress-induced premature senescence biological process from the curated GO Biological Process Annotations dataset.

regulation of activation-induced cell death of t cells Gene Set

From GO Biological Process Annotations

genes participating in the regulation of activation-induced cell death of t cells biological process from the curated GO Biological Process Annotations dataset.

positive regulation of activation-induced cell death of t cells Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of activation-induced cell death of t cells biological process from the curated GO Biological Process Annotations dataset.

regulation of endoplasmic reticulum stress-induced neuron intrinsic apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of endoplasmic reticulum stress-induced neuron intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

negative regulation of transcription from rna polymerase ii promoter in response to uv-induced dna damage Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of transcription from rna polymerase ii promoter in response to uv-induced dna damage biological process from the curated GO Biological Process Annotations dataset.

regulation of transcription from rna polymerase ii promoter in response to uv-induced dna damage Gene Set

From GO Biological Process Annotations

genes participating in the regulation of transcription from rna polymerase ii promoter in response to uv-induced dna damage biological process from the curated GO Biological Process Annotations dataset.

negative regulation of hydrogen peroxide-induced neuron death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of hydrogen peroxide-induced neuron death biological process from the curated GO Biological Process Annotations dataset.

regulation of oxidative stress-induced cell death Gene Set

From GO Biological Process Annotations

genes participating in the regulation of oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations dataset.

oxidative stress-induced premature senescence Gene Set

From GO Biological Process Annotations

genes participating in the oxidative stress-induced premature senescence biological process from the curated GO Biological Process Annotations dataset.

negative regulation of endoplasmic reticulum stress-induced neuron intrinsic apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of endoplasmic reticulum stress-induced neuron intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of hydrogen peroxide-induced neuron death Gene Set

From GO Biological Process Annotations

genes participating in the regulation of hydrogen peroxide-induced neuron death biological process from the curated GO Biological Process Annotations dataset.

regulation of hydrogen peroxide-induced cell death Gene Set

From GO Biological Process Annotations

genes participating in the regulation of hydrogen peroxide-induced cell death biological process from the curated GO Biological Process Annotations dataset.

host programmed cell death induced by symbiont Gene Set

From GO Biological Process Annotations

genes participating in the host programmed cell death induced by symbiont biological process from the curated GO Biological Process Annotations dataset.

regulation of oxidative stress-induced neuron death Gene Set

From GO Biological Process Annotations

genes participating in the regulation of oxidative stress-induced neuron death biological process from the curated GO Biological Process Annotations dataset.

negative regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

negative regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

double-strand break repair via break-induced replication Gene Set

From GO Biological Process Annotations

genes participating in the double-strand break repair via break-induced replication biological process from the curated GO Biological Process Annotations dataset.

regulation of hydrogen peroxide-induced neuron intrinsic apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of hydrogen peroxide-induced neuron intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

calcium-induced calcium release activity Gene Set

From GO Molecular Function Annotations

genes performing the calcium-induced calcium release activity molecular function from the curated GO Molecular Function Annotations dataset.

Drug-induced liver injury Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Drug-induced liver injury phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Asthma (toluene diisocyanate-induced) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Asthma (toluene diisocyanate-induced) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Antipsychotic-induced QTc interval prolongation Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Antipsychotic-induced QTc interval prolongation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Nevirapine-induced rash Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Nevirapine-induced rash phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Drug-induced liver injury (amoxicillin-clavulanate) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Drug-induced liver injury (amoxicillin-clavulanate) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Paclitaxel-induced neuropathy Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Paclitaxel-induced neuropathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Epirubicin-induced leukopenia Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Epirubicin-induced leukopenia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Insomnia (caffeine-induced) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Insomnia (caffeine-induced) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Drug-induced torsades de pointes Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Drug-induced torsades de pointes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Psychosis (methamphetamine induced) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Psychosis (methamphetamine induced) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Thiazide-induced adverse metabolic effects in hypertensive patients Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Thiazide-induced adverse metabolic effects in hypertensive patients phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Ribavirin-induced anemia Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Ribavirin-induced anemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Hepatitis C induced liver cirrhosis Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Hepatitis C induced liver cirrhosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Drug-induced liver injury (flucloxacillin) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Drug-induced liver injury (flucloxacillin) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Hepatitis C induced liver fibrosis Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Hepatitis C induced liver fibrosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

drug-induced hepatitis Gene Set

From GWASdb SNP-Disease Associations

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

drug-induced mental disorder Gene Set

From GWASdb SNP-Disease Associations

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

substance-induced psychosis Gene Set

From GWASdb SNP-Disease Associations

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

alcohol-induced mental disorder Gene Set

From 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.

aspirin-induced asthma Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the aspirin-induced asthma phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

impaired collagen-induced platelet aggregation Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired collagen-induced platelet aggregation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired adp-induced platelet aggregation Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired adp-induced platelet aggregation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

nystagmus-induced head nodding Gene Set

From HPO Gene-Disease Associations

genes associated with the nystagmus-induced head nodding phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

fava bean-induced hemolytic anemia Gene Set

From HPO Gene-Disease Associations

genes associated with the fava bean-induced hemolytic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

chromosomal breakage induced by crosslinking agents Gene Set

From HPO Gene-Disease Associations

genes associated with the chromosomal breakage induced by crosslinking agents phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

chromosomal breakage induced by ionizing radiation Gene Set

From HPO Gene-Disease Associations

genes associated with the chromosomal breakage induced by ionizing radiation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired thrombin-induced platelet aggregation Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired thrombin-induced platelet aggregation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

percussion-induced rapid rolling muscle contractions (pirc) Gene Set

From HPO Gene-Disease Associations

genes associated with the percussion-induced rapid rolling muscle contractions (pirc) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

warfarin-induced skin necrosis Gene Set

From HPO Gene-Disease Associations

genes associated with the warfarin-induced skin necrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

deficient excision of uv-induced pyrimidine dimers in dna Gene Set

From HPO Gene-Disease Associations

genes associated with the deficient excision of uv-induced pyrimidine dimers in dna phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aspirin-induced asthma Gene Set

From HPO Gene-Disease Associations

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

stress/infection-induced lactic acidosis Gene Set

From HPO Gene-Disease Associations

genes associated with the stress/infection-induced lactic acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired epinephrine-induced platelet aggregation Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired epinephrine-induced platelet aggregation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

effort-induced polymorphic ventricular tachycardias Gene Set

From HPO Gene-Disease Associations

genes associated with the effort-induced polymorphic ventricular tachycardias phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Neoplasms, Radiation-Induced Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Dyskinesia, Drug-Induced Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Alcohol-Induced Disorders, Nervous System Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Alcohol-Induced Disorders, Nervous System phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Alcohol-Induced Disorders Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Drug-Induced Liver Injury Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Drug-Induced Liver Injury phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Asthma, Aspirin-Induced Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Psychoses, Substance-Induced Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Hypertension, Pregnancy-Induced Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Leukemia, Radiation-Induced Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Hearing Loss, Noise-Induced Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hearing Loss, Noise-Induced phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Drug-Induced Liver Injury, Chronic Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Drug-Induced Liver Injury, Chronic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Abnormalities, Drug-Induced Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Akathisia, Drug-Induced Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Signal-induced proliferation-associated 1-like protein, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Signal-induced proliferation-associated 1-like protein, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

TGF beta-induced protein bIGH3/osteoblast-specific factor 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the TGF beta-induced protein bIGH3/osteoblast-specific factor 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Insulin-induced gene 1 protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Insulin-induced gene 1 protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

LPS-induced tumour necrosis factor alpha factor Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the LPS-induced tumour necrosis factor alpha factor protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Phorbol-12-myristate-13-acetate-induced protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Phorbol-12-myristate-13-acetate-induced protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

P53-induced protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the P53-induced protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Dexamethasone-induced protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Dexamethasone-induced protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Hypoxia induced protein, domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Hypoxia induced protein, domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Etoposide-induced 2.4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Etoposide-induced 2.4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Drought induced 19 protein-like, zinc-binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Drought induced 19 protein-like, zinc-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

RNA-induced silencing complex, nuclease component Tudor-SN Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the RNA-induced silencing complex, nuclease component Tudor-SN protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Interferon-induced protein with tetratricopeptide repeats 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Interferon-induced protein with tetratricopeptide repeats 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Interferon-induced protein with tetratricopeptide repeats 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Interferon-induced protein with tetratricopeptide repeats 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Interferon-induced protein with tetratricopeptide repeats 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Interferon-induced protein with tetratricopeptide repeats 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transforming growth factor beta-1-induced transcript 1 protein/Leupaxin Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transforming growth factor beta-1-induced transcript 1 protein/Leupaxin protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Interferon-induced protein 44 family Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Interferon-induced protein 44 family protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Insulin-induced protein family Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Insulin-induced protein family protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Oxidative stress-induced growth inhibitor 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Oxidative stress-induced growth inhibitor 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Oxidative stress-induced growth inhibitor 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Oxidative stress-induced growth inhibitor 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucocorticoid-induced transcript 1 protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucocorticoid-induced transcript 1 protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Interferon-induced protein with tetratricopeptide repeat 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Interferon-induced protein with tetratricopeptide repeat 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Arginine vasopressin-induced protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Arginine vasopressin-induced protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Retinoic acid-induced protein 2/sine oculis-binding protein homologue Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Retinoic acid-induced protein 2/sine oculis-binding protein homologue protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Progesterone-induced-blocking factor 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Progesterone-induced-blocking factor 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Retinoic acid induced 16-like protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Retinoic acid induced 16-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Decidual protein, progesterone induced Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Decidual protein, progesterone induced protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Caffeine-induced death protein 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Caffeine-induced death protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucocorticoid-induced transcript 1/FAM117 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucocorticoid-induced transcript 1/FAM117 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal xenobiotic induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal xenobiotic induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased mortality induced by gamma-irradiation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased mortality induced by gamma-irradiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to induced joint inflammation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to induced joint inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased response of heart to induced stress Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased response of heart to induced stress phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased mortality induced by ionizing radiation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased mortality induced by ionizing radiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to induced choroid neovascularization Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to induced choroid neovascularization phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased activation-induced b cell apoptosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased activation-induced b cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased sensitivity to induced cell death Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased sensitivity to induced cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to ototoxicity-induced hearing loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to ototoxicity-induced hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased sensitivity to xenobiotic induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased sensitivity to xenobiotic induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased sensitivity to induced cell death Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased sensitivity to induced cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to bacterial infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to bacterial infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased incidence of induced tumors Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased incidence of induced tumors phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased response of heart to induced stress Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased response of heart to induced stress phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to induced pancreatitis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to induced pancreatitis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased sensitivity to induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased sensitivity to induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

environmentally induced seizures Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the environmentally induced seizures phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal induced retinal neovascularization Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal induced retinal neovascularization phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal induced cell death Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal induced cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to bacterial infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to bacterial infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal response to stress-induced hyperthermia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal response to stress-induced hyperthermia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased activation-induced cell death of t cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased activation-induced cell death of t cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to induced colitis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to induced colitis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased response to stress-induced hyperthermia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased response to stress-induced hyperthermia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to viral infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to viral infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased sensitivity to induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased sensitivity to induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased mortality induced by ionizing radiation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased mortality induced by ionizing radiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to induced colitis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to induced colitis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

altered response of heart to induced stress Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the altered response of heart to induced stress phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to induced arthritis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to induced arthritis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased activation-induced b cell apoptosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased activation-induced b cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to noise-induced hearing loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to noise-induced hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to parasitic infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to parasitic infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to induced muscular atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to pharmacologically induced seizures Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to pharmacologically induced seizures phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to induced retinal damage Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to induced retinal damage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to induced pancreatitis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to induced pancreatitis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to induced muscular atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal activation-induced b cell apoptosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal activation-induced b cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to diet-induced obesity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to diet-induced obesity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to viral infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to viral infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to induced choroidal neovascularization Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to induced choroidal neovascularization phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to parasitic infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to parasitic infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to induced arthritis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to induced arthritis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to noise-induced hearing loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to noise-induced hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal incidence of induced tumors Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal incidence of induced tumors phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal mortality induced by ionizing radiation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal mortality induced by ionizing radiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

altered susceptibility to infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the altered susceptibility to infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased incidence of induced tumors Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased incidence of induced tumors phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to diet-induced obesity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to diet-induced obesity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to pharmacologically induced seizures Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to pharmacologically induced seizures phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal activation-induced cell death of t cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal activation-induced cell death of t cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased sensitivity to xenobiotic induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased sensitivity to xenobiotic induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

induced hyperactivity Gene Set

From MPO Gene-Phenotype Associations

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

induced chromosome breakage Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the induced chromosome breakage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal susceptibility to induced colitis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal susceptibility to induced colitis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal sensitivity to induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal sensitivity to induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased response to stress-induced hyperthermia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased response to stress-induced hyperthermia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

{encephalopathy, acute, infection-induced, susceptibility to, 6} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {encephalopathy, acute, infection-induced, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.

rhabdomyolysis, cerivastatin-induced Gene Set

From OMIM Gene-Disease Associations

genes associated with the rhabdomyolysis, cerivastatin-induced phenotype from the curated OMIM Gene-Disease Associations dataset.

familial cold-induced inflammatory syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the familial cold-induced inflammatory syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

{encephalopathy, acute, infection-induced, 3, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {encephalopathy, acute, infection-induced, 3, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{angioedema induced by ace inhibitors, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {angioedema induced by ace inhibitors, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{encephalopathy, acute, infection-induced, 4, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {encephalopathy, acute, infection-induced, 4, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hypersensitivity syndrome, carbamazepine-induced, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hypersensitivity syndrome, carbamazepine-induced, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{asthma, aspirin-induced, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {asthma, aspirin-induced, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{?hearing loss, cisplatin-induced, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {?hearing loss, cisplatin-induced, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{drug-induced liver injury due to flucloxacillin} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {drug-induced liver injury due to flucloxacillin} phenotype from the curated OMIM Gene-Disease Associations dataset.

osteomalacia, tumor-induced Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteomalacia, tumor-induced phenotype from the curated OMIM Gene-Disease Associations dataset.

{uv-induced skin damage} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {uv-induced skin damage} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hypertension, pregnancy-induced} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hypertension, pregnancy-induced} phenotype from the curated OMIM Gene-Disease Associations dataset.

cold-induced sweating syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cold-induced sweating syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

cold-induced sweating syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cold-induced sweating syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

meningioma, radiation-induced Gene Set

From OMIM Gene-Disease Associations

genes associated with the meningioma, radiation-induced phenotype from the curated OMIM Gene-Disease Associations dataset.

agonist-induced Gene Set

From Phosphosite Textmining Biological Term Annotations

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

egf-induced Gene Set

From Phosphosite Textmining Biological Term Annotations

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

DNA Damage/Telomere Stress Induced Senescence Gene Set

From Reactome Pathways

proteins participating in the DNA Damage/Telomere Stress Induced Senescence pathway from the Reactome Pathways dataset.

Oncogene Induced Senescence Gene Set

From Reactome Pathways

proteins participating in the Oncogene Induced Senescence pathway from the Reactome Pathways dataset.

Influenza Virus Induced Apoptosis Gene Set

From Reactome Pathways

proteins participating in the Influenza Virus Induced Apoptosis pathway from the Reactome Pathways dataset.

Calmodulin induced events Gene Set

From Reactome Pathways

proteins participating in the Calmodulin induced events pathway from the Reactome Pathways dataset.

Apoptosis induced DNA fragmentation Gene Set

From Reactome Pathways

proteins participating in the Apoptosis induced DNA fragmentation pathway from the Reactome Pathways dataset.

Oxidative Stress Induced Senescence Gene Set

From Reactome Pathways

proteins participating in the Oxidative Stress Induced Senescence pathway from the Reactome Pathways dataset.

Butyrate-induced histone acetylation(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Butyrate-induced histone acetylation(Homo sapiens) pathway from the Wikipathways Pathways dataset.

basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression Gene Set

From Biocarta Pathways

proteins participating in the basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression pathway from the Biocarta Pathways dataset.

BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Coloboma, uveal, with cleft lip and palate and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Coloboma, uveal, with cleft lip and palate and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diabetes mellitus AND insipidus with optic atrophy AND deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset.

Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation from the curated CTD Gene-Disease Associations dataset.

Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities from the curated CTD Gene-Disease Associations dataset.

Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia from the curated CTD Gene-Disease Associations dataset.

Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux from the curated CTD Gene-Disease Associations dataset.

Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations from the curated CTD Gene-Disease Associations dataset.

postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anxiety and hostility and depression Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

genes associated with the disease charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

frontotemporal dementia and pick-like 3r and 4r tauopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease frontotemporal dementia and pick-like 3r and 4r tauopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

squamous cell carcinomas of the head and neck (scchn) and breast cancer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease squamous cell carcinomas of the head and neck (scchn) and breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

vitamins and metabolites in pregnant women and neonates Gene Set

From GAD Gene-Disease Associations

genes associated with the disease vitamins and metabolites in pregnant women and neonates in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

racemase and epimerase activity, acting on amino acids and derivatives Gene Set

From GO Molecular Function Annotations

genes performing the racemase and epimerase activity, acting on amino acids and derivatives molecular function from the curated GO Molecular Function Annotations dataset.

racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set

From GO Molecular Function Annotations

genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations dataset.

leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation phenotype from the curated OMIM Gene-Disease Associations dataset.

microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma Gene Set

From OMIM Gene-Disease Associations

genes associated with the microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset.

hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Set

From Reactome Pathways

proteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways dataset.

Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Set

From Reactome Pathways

proteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways dataset.

PI and PC transport between ER and Golgi membranes Gene Set

From Reactome Pathways

proteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways dataset.

Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Set

From Reactome Pathways

proteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways dataset.

FGFR1c and Klotho ligand binding and activation Gene Set

From Reactome Pathways

proteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways dataset.

Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Set

From Reactome Pathways

proteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways dataset.

Synthesis and processing of ENV and VPU Gene Set

From Reactome Pathways

proteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways dataset.

Synthesis and interconversion of nucleotide di- and triphosphates Gene Set

From Reactome Pathways

proteins participating in the Synthesis and interconversion of nucleotide di- and triphosphates pathway from the Reactome Pathways dataset.

SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) pathway from the Wikipathways Pathways dataset.

SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) pathway from the Wikipathways Pathways dataset.

SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Basic cell groups and regions Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Basic cell groups and regions relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

head and face region of M1 Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in head and face region of M1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

telomeres telomerase cellular aging and immortality Gene Set

From Biocarta Pathways

proteins participating in the telomeres telomerase cellular aging and immortality pathway from the Biocarta Pathways dataset.

mcalpain and friends in cell motility Gene Set

From Biocarta Pathways

proteins participating in the mcalpain and friends in cell motility pathway from the Biocarta Pathways dataset.

role of ppar-gamma coactivators in obesity and thermogenesis Gene Set

From Biocarta Pathways

proteins participating in the role of ppar-gamma coactivators in obesity and thermogenesis pathway from the Biocarta Pathways dataset.

il12 and stat4 dependent signaling pathway in th1 development Gene Set

From Biocarta Pathways

proteins participating in the il12 and stat4 dependent signaling pathway in th1 development pathway from the Biocarta Pathways dataset.

hypoxia and p53 in the cardiovascular system Gene Set

From Biocarta Pathways

proteins participating in the hypoxia and p53 in the cardiovascular system pathway from the Biocarta Pathways dataset.

lissencephaly gene (lis1) in neuronal migration and development Gene Set

From Biocarta Pathways

proteins participating in the lissencephaly gene (lis1) in neuronal migration and development pathway from the Biocarta Pathways dataset.

role of erbb2 in signal transduction and oncology Gene Set

From Biocarta Pathways

proteins participating in the role of erbb2 in signal transduction and oncology pathway from the Biocarta Pathways dataset.

corticosteroids and cardioprotection Gene Set

From Biocarta Pathways

proteins participating in the corticosteroids and cardioprotection pathway from the Biocarta Pathways dataset.

cyclins and cell cycle regulation Gene Set

From Biocarta Pathways

proteins participating in the cyclins and cell cycle regulation pathway from the Biocarta Pathways dataset.

mechanism of acetaminophen activity and toxicity Gene Set

From Biocarta Pathways

proteins participating in the mechanism of acetaminophen activity and toxicity pathway from the Biocarta Pathways dataset.

nfat and hypertrophy of the heart Gene Set

From Biocarta Pathways

proteins participating in the nfat and hypertrophy of the heart pathway from the Biocarta Pathways dataset.

acetylation and deacetylation of rela in nucleus Gene Set

From Biocarta Pathways

proteins participating in the acetylation and deacetylation of rela in nucleus pathway from the Biocarta Pathways dataset.

thrombin signaling and protease-activated receptors Gene Set

From Biocarta Pathways

proteins participating in the thrombin signaling and protease-activated receptors pathway from the Biocarta Pathways dataset.

antigen processing and presentation Gene Set

From Biocarta Pathways

proteins participating in the antigen processing and presentation pathway from the Biocarta Pathways dataset.

stathmin and breast cancer resistance to antimicrotubule agents Gene Set

From Biocarta Pathways

proteins participating in the stathmin and breast cancer resistance to antimicrotubule agents pathway from the Biocarta Pathways dataset.

role of ß-arrestins in the activation and targeting of map kinases Gene Set

From Biocarta Pathways

proteins participating in the role of ß-arrestins in the activation and targeting of map kinases pathway from the Biocarta Pathways dataset.

cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway Gene Set

From Biocarta Pathways

proteins participating in the cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway pathway from the Biocarta Pathways dataset.

role of pi3k subunit p85 in regulation of actin organization and cell migration Gene Set

From Biocarta Pathways

proteins participating in the role of pi3k subunit p85 in regulation of actin organization and cell migration pathway from the Biocarta Pathways dataset.

btg family proteins and cell cycle regulation Gene Set

From Biocarta Pathways

proteins participating in the btg family proteins and cell cycle regulation pathway from the Biocarta Pathways dataset.

control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) Gene Set

From Biocarta Pathways

proteins participating in the control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) pathway from the Biocarta Pathways dataset.

endocytotic role of ndk phosphins and dynamin Gene Set

From Biocarta Pathways

proteins participating in the endocytotic role of ndk phosphins and dynamin pathway from the Biocarta Pathways dataset.

regulation of eif-4e and p70s6 kinase Gene Set

From Biocarta Pathways

proteins participating in the regulation of eif-4e and p70s6 kinase pathway from the Biocarta Pathways dataset.

estrogen responsive protein efp controls cell cycle and breast tumors growth Gene Set

From Biocarta Pathways

proteins participating in the estrogen responsive protein efp controls cell cycle and breast tumors growth pathway from the Biocarta Pathways dataset.

vegf hypoxia and angiogenesis Gene Set

From Biocarta Pathways

proteins participating in the vegf hypoxia and angiogenesis pathway from the Biocarta Pathways dataset.

yaci and bcma stimulation of b cell immune responses Gene Set

From Biocarta Pathways

proteins participating in the yaci and bcma stimulation of b cell immune responses pathway from the Biocarta Pathways dataset.

lck and fyn tyrosine kinases in initiation of tcr activation Gene Set

From Biocarta Pathways

proteins participating in the lck and fyn tyrosine kinases in initiation of tcr activation pathway from the Biocarta Pathways dataset.

hiv-1 nef: negative effector of fas and tnf Gene Set

From Biocarta Pathways

proteins participating in the hiv-1 nef: negative effector of fas and tnf pathway from the Biocarta Pathways dataset.

nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells Gene Set

From Biocarta Pathways

proteins participating in the nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells pathway from the Biocarta Pathways dataset.

ucalpain and friends in cell spread Gene Set

From Biocarta Pathways

proteins participating in the ucalpain and friends in cell spread pathway from the Biocarta Pathways dataset.

ionomycin and phorbal ester signaling pathway Gene Set

From Biocarta Pathways

proteins participating in the ionomycin and phorbal ester signaling pathway pathway from the Biocarta Pathways dataset.

carm1 and regulation of the estrogen receptor Gene Set

From Biocarta Pathways

proteins participating in the carm1 and regulation of the estrogen receptor pathway from the Biocarta Pathways dataset.

phosphoinositides and their downstream targets Gene Set

From Biocarta Pathways

proteins participating in the phosphoinositides and their downstream targets pathway from the Biocarta Pathways dataset.

melanocyte development and pigmentation pathway Gene Set

From Biocarta Pathways

proteins participating in the melanocyte development and pigmentation pathway pathway from the Biocarta Pathways dataset.

akap95 role in mitosis and chromosome dynamics Gene Set

From Biocarta Pathways

proteins participating in the akap95 role in mitosis and chromosome dynamics pathway from the Biocarta Pathways dataset.

transcription factor creb and its extracellular signals Gene Set

From Biocarta Pathways

proteins participating in the transcription factor creb and its extracellular signals pathway from the Biocarta Pathways dataset.

visceral fat deposits and the metabolic syndrome Gene Set

From Biocarta Pathways

proteins participating in the visceral fat deposits and the metabolic syndrome pathway from the Biocarta Pathways dataset.

the igf-1 receptor and longevity Gene Set

From Biocarta Pathways

proteins participating in the the igf-1 receptor and longevity pathway from the Biocarta Pathways dataset.

cdc25 and chk1 regulatory pathway in response to dna damage Gene Set

From Biocarta Pathways

proteins participating in the cdc25 and chk1 regulatory pathway in response to dna damage pathway from the Biocarta Pathways dataset.

human cytomegalovirus and map kinase pathways Gene Set

From Biocarta Pathways

proteins participating in the human cytomegalovirus and map kinase pathways pathway from the Biocarta Pathways dataset.

influence of ras and rho proteins on g1 to s transition Gene Set

From Biocarta Pathways

proteins participating in the influence of ras and rho proteins on g1 to s transition pathway from the Biocarta Pathways dataset.

proteolysis and signaling pathway of notch Gene Set

From Biocarta Pathways

proteins participating in the proteolysis and signaling pathway of notch pathway from the Biocarta Pathways dataset.

apoptotic dna-fragmentation and tissue homeostasis Gene Set

From Biocarta Pathways

proteins participating in the apoptotic dna-fragmentation and tissue homeostasis pathway from the Biocarta Pathways dataset.

ion channels and their functional role in vascular endothelium Gene Set

From Biocarta Pathways

proteins participating in the ion channels and their functional role in vascular endothelium pathway from the Biocarta Pathways dataset.

alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease Gene Set

From Biocarta Pathways

proteins participating in the alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease pathway from the Biocarta Pathways dataset.

fosb gene expression and drug abuse Gene Set

From Biocarta Pathways

proteins participating in the fosb gene expression and drug abuse pathway from the Biocarta Pathways dataset.

links between pyk2 and map kinases Gene Set

From Biocarta Pathways

proteins participating in the links between pyk2 and map kinases pathway from the Biocarta Pathways dataset.

opposing roles of aif in apoptosis and cell survival Gene Set

From Biocarta Pathways

proteins participating in the opposing roles of aif in apoptosis and cell survival pathway from the Biocarta Pathways dataset.

degradation of the rar and rxr by the proteasome Gene Set

From Biocarta Pathways

proteins participating in the degradation of the rar and rxr by the proteasome pathway from the Biocarta Pathways dataset.

cadmium induces dna synthesis and proliferation in macrophages Gene Set

From Biocarta Pathways

proteins participating in the cadmium induces dna synthesis and proliferation in macrophages pathway from the Biocarta Pathways dataset.

erk and pi-3 kinase are necessary for collagen binding in corneal epithelia Gene Set

From Biocarta Pathways

proteins participating in the erk and pi-3 kinase are necessary for collagen binding in corneal epithelia pathway from the Biocarta Pathways dataset.

role of brca1 brca2 and atr in cancer susceptibility Gene Set

From Biocarta Pathways

proteins participating in the role of brca1 brca2 and atr in cancer susceptibility pathway from the Biocarta Pathways dataset.

chrebp regulation by carbohydrates and camp Gene Set

From Biocarta Pathways

proteins participating in the chrebp regulation by carbohydrates and camp pathway from the Biocarta Pathways dataset.

pten dependent cell cycle arrest and apoptosis Gene Set

From Biocarta Pathways

proteins participating in the pten dependent cell cycle arrest and apoptosis pathway from the Biocarta Pathways dataset.

induction of apoptosis through dr3 and dr4/5 death receptors Gene Set

From Biocarta Pathways

proteins participating in the induction of apoptosis through dr3 and dr4/5 death receptors pathway from the Biocarta Pathways dataset.

CIITA-18437201-Raji B cells and iDC-human Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CIITA-18437201-Raji B cells and iDC-human transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

VDR-23401126-LCL-AND-THP1-HUMAN Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the VDR-23401126-LCL-AND-THP1-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

BACH1-22875853-HELA-AND-SCP4-HUMAN Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the BACH1-22875853-HELA-AND-SCP4-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

Hypothyroidism, central, and testicular enlargement Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypothyroidism, central, and testicular enlargement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Trifunctional protein deficiency with myopathy and neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Trifunctional protein deficiency with myopathy and neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Foveal hypoplasia and presenile cataract syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Foveal hypoplasia and presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arthrogryposis, mental retardation, and seizures Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arthrogryposis, mental retardation, and seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Vater association with macrocephaly and ventriculomegaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Vater association with macrocephaly and ventriculomegaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal hamartomas nephroblastomatosis and fetal gigantism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal hamartomas nephroblastomatosis and fetal gigantism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, lactic acidosis, and sideroblastic anemia 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microtia, hearing impairment, and cleft palate Gene Set