Neonatal Stroke

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Results for "Neonatal Stroke": 615 gene sets

Name
Neonatal Stroke Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Stroke in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
encephalitis; glucosephosphate dehydrogenase deficiency; jaundice, neonatal; neonatal jaundice Gene Set From GAD Gene-Disease Associations genes associated with the disease encephalitis; glucosephosphate dehydrogenase deficiency; jaundice, neonatal; neonatal jaundice in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
jaundice, neonatal; neonatal jaundice Gene Set From GAD Gene-Disease Associations genes associated with the disease jaundice, neonatal; neonatal jaundice in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glucosephosphate dehydrogenase deficiency; hemolysis; jaundice, neonatal; neonatal jaundice Gene Set From GAD Gene-Disease Associations genes associated with the disease glucosephosphate dehydrogenase deficiency; hemolysis; jaundice, neonatal; neonatal jaundice in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular disease; stroke; stroke, ischemic Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular disease; stroke; stroke, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stroke, ischemic; stroke, hemorrhagic Gene Set From GAD Gene-Disease Associations genes associated with the disease stroke, ischemic; stroke, hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain hemorrhage; stroke; stroke, lacunar Gene Set From GAD Gene-Disease Associations genes associated with the disease brain hemorrhage; stroke; stroke, lacunar in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Transient neonatal diabetes mellitus 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Transient neonatal diabetes mellitus 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign familial neonatal-infantile seizures Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal-infantile seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neonatal insulin-dependent diabetes mellitus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neonatal insulin-dependent diabetes mellitus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign familial neonatal seizures 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal seizures 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign familial neonatal seizures 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal seizures 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperparathyroidism, neonatal severe Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperparathyroidism, neonatal severe phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inflammatory skin and bowel disease, neonatal, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diabetes mellitus, permanent neonatal, with neurologic features Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diabetes mellitus, permanent neonatal, with neurologic features phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rigidity and multifocal seizure syndrome, lethal neonatal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rigidity and multifocal seizure syndrome, lethal neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL Gene Set From ClinVar Gene-Phenotype Associations genes associated with the CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inflammatory skin and bowel disease, neonatal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neonatal adrenoleucodystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neonatal adrenoleucodystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Permanent neonatal diabetes mellitus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Permanent neonatal diabetes mellitus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neonatal intrahepatic cholestasis caused by citrin deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neonatal intrahepatic cholestasis caused by citrin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diabetes mellitus, permanent neonatal, with cerebellar agenesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diabetes mellitus, permanent neonatal, with cerebellar agenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cyanosis, transient neonatal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cyanosis, transient neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neonatal diabetes mellitus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neonatal diabetes mellitus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal from the curated CTD Gene-Disease Associations dataset.
Hyperparathyroidism, Neonatal Severe Primary Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperparathyroidism, Neonatal Severe Primary from the curated CTD Gene-Disease Associations dataset.
Neonatal-onset citrullinemia type 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neonatal-onset citrullinemia type 2 from the curated CTD Gene-Disease Associations dataset.
Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress from the curated CTD Gene-Disease Associations dataset.
Diabetes Mellitus, Permanent Neonatal, with Cerebellar Agenesis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diabetes Mellitus, Permanent Neonatal, with Cerebellar Agenesis 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.
Jaundice, Neonatal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Jaundice, Neonatal from the curated CTD Gene-Disease Associations dataset.
SEIZURES, BENIGN FAMILIAL NEONATAL, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL NEONATAL, 2 from the curated CTD Gene-Disease Associations dataset.
Diabetes Mellitus, Transient Neonatal, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diabetes Mellitus, Transient Neonatal, 3 from the curated CTD Gene-Disease Associations dataset.
Diabetes Mellitus, Transient Neonatal, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diabetes Mellitus, Transient Neonatal, 1 from the curated CTD Gene-Disease Associations dataset.
Finnish lethal neonatal metabolic syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Finnish lethal neonatal metabolic syndrome from the curated CTD Gene-Disease Associations dataset.
Diabetes Mellitus, Transient Neonatal, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diabetes Mellitus, Transient Neonatal, 2 from the curated CTD Gene-Disease Associations dataset.
Pancreatic beta cell agenesis with neonatal diabetes mellitus Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pancreatic beta cell agenesis with neonatal diabetes mellitus from the curated CTD Gene-Disease Associations dataset.
Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism from the curated CTD Gene-Disease Associations dataset.
Hyperbilirubinemia, Transient Familial Neonatal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperbilirubinemia, Transient Familial Neonatal from the curated CTD Gene-Disease Associations dataset.
Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations from the curated CTD Gene-Disease Associations dataset.
Diabetes Mellitus, Permanent Neonatal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diabetes Mellitus, Permanent Neonatal from the curated CTD Gene-Disease Associations dataset.
Neonatal Abstinence Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neonatal Abstinence Syndrome 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, 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.
SEIZURES, BENIGN FAMILIAL NEONATAL, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL NEONATAL, 1 from the curated CTD Gene-Disease Associations dataset.
Anemia, Neonatal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anemia, Neonatal from the curated CTD Gene-Disease Associations dataset.
Thrombocytopenia, Neonatal Alloimmune Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thrombocytopenia, Neonatal Alloimmune from the curated CTD Gene-Disease Associations dataset.
neonatal period electroclinical syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease neonatal period electroclinical syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
neonatal candidiasis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neonatal candidiasis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neonatal anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neonatal anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign neonatal seizures Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign neonatal seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neonatal leukemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neonatal leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neonatal diabetes mellitus Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neonatal diabetes mellitus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
transient neonatal neutropenia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease transient neonatal neutropenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neonatal jaundice Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neonatal jaundice in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neonatal period electroclinical syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neonatal period electroclinical syndrome 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 Association 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.
neonatal thyrotoxicosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neonatal thyrotoxicosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neonatal abstinence syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neonatal abstinence syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neonatal myasthenia gravis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neonatal myasthenia gravis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neonatal respiratory failure Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neonatal respiratory failure in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
transient neonatal thrombocytopenia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease transient neonatal thrombocytopenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
glucosephosphate dehydrogenase deficiency; hyperbilirubinemia, neonatal Gene Set From GAD Gene-Disease Associations genes associated with the disease glucosephosphate dehydrogenase deficiency; hyperbilirubinemia, neonatal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; hyperbilirubinemia, neonatal Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; hyperbilirubinemia, neonatal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
resp distress syndrome neonatal; respiratory distress syndrome, newborn Gene Set From GAD Gene-Disease Associations genes associated with the disease resp distress syndrome neonatal; respiratory distress syndrome, newborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperbilirubinemia, neonatal Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperbilirubinemia, neonatal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obstetric labor, premature; resp distress syndrome neonatal; respiratory distress syndrome, newborn; tachycardia Gene Set From GAD Gene-Disease Associations genes associated with the disease obstetric labor, premature; resp distress syndrome neonatal; respiratory distress syndrome, newborn; tachycardia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections Gene Set From GAD Gene-Disease Associations genes associated with the disease bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neonatal thrombocytopenia Gene Set From GAD Gene-Disease Associations genes associated with the disease neonatal thrombocytopenia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lung diseases; resp distress syndrome neonatal; respiratory distress syndrome, newborn Gene Set From GAD Gene-Disease Associations genes associated with the disease lung diseases; resp distress syndrome neonatal; respiratory distress syndrome, newborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bronchopulmonary dysplasia; respiratory distress syndrome, neonatal Gene Set From GAD Gene-Disease Associations genes associated with the disease bronchopulmonary dysplasia; respiratory distress syndrome, neonatal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
respiratory distress syndrome, neonatal Gene Set From GAD Gene-Disease Associations genes associated with the disease respiratory distress syndrome, neonatal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
citrullinemia, adult-onset type ii; hepatitis, neonatal associated with cholestasis Gene Set From GAD Gene-Disease Associations genes associated with the disease citrullinemia, adult-onset type ii; hepatitis, neonatal associated with cholestasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neonatal infection Gene Set From GAD Gene-Disease Associations genes associated with the disease neonatal infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neonatal hyperbilirubinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease neonatal hyperbilirubinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperbilirubinemia, neonatal; jaundice Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperbilirubinemia, neonatal; jaundice in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cutaneous neonatal lupus Gene Set From GAD Gene-Disease Associations genes associated with the disease cutaneous neonatal lupus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
jaundice, neonatal Gene Set From GAD Gene-Disease Associations genes associated with the disease jaundice, neonatal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute neonatal disease and hyperammonemia Gene Set From GAD Gene-Disease Associations genes associated with the disease acute neonatal disease and hyperammonemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neonatal sepsis Gene Set From GAD Gene-Disease Associations genes associated with the disease neonatal sepsis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neonatal Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term neonatal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
KDM4C_natural variation_GSE41040_589_human_fibroblasts fron neonatal foreskin Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the KDM4C_natural variation_GSE41040_589_human_fibroblasts fron neonatal foreskin gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
KDM4C_natural variation_GSE41040_588_human_fibroblasts fron neonatal foreskin Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the KDM4C_natural variation_GSE41040_588_human_fibroblasts fron neonatal foreskin gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
KDM4C_natural variation_GSE41040_590_human_fibroblasts fron neonatal foreskin Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the KDM4C_natural variation_GSE41040_590_human_fibroblasts fron neonatal foreskin gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
Neonatal lupus Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Neonatal lupus phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
neonatal unconjugated hyperbilirubinemia Gene Set From HPO Gene-Disease Associations genes associated with the neonatal unconjugated hyperbilirubinemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal hyperbilirubinemia Gene Set From HPO Gene-Disease Associations genes associated with the neonatal hyperbilirubinemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal breathing dysregulation Gene Set From HPO Gene-Disease Associations genes associated with the neonatal breathing dysregulation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal alloimmune thrombocytopenia Gene Set From HPO Gene-Disease Associations genes associated with the neonatal alloimmune thrombocytopenia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal epiphyseal stippling Gene Set From HPO Gene-Disease Associations genes associated with the neonatal epiphyseal stippling phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal short-trunk short stature Gene Set From HPO Gene-Disease Associations genes associated with the neonatal short-trunk short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal death Gene Set From HPO Gene-Disease Associations genes associated with the neonatal death phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal insulin-dependent diabetes mellitus Gene Set From HPO Gene-Disease Associations genes associated with the neonatal insulin-dependent diabetes mellitus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal hypotonia Gene Set From HPO Gene-Disease Associations genes associated with the neonatal hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal wrinkled skin of hands and feet Gene Set From HPO Gene-Disease Associations genes associated with the neonatal wrinkled skin of hands and feet phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized neonatal hypotonia Gene Set From HPO Gene-Disease Associations genes associated with the generalized neonatal hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spontaneous neonatal pneumothorax Gene Set From HPO Gene-Disease Associations genes associated with the spontaneous neonatal pneumothorax phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal respiratory distress Gene Set From HPO Gene-Disease Associations genes associated with the neonatal respiratory distress phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
transient neonatal diabetes mellitus Gene Set From HPO Gene-Disease Associations genes associated with the transient neonatal diabetes mellitus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal short-limb short stature Gene Set From HPO Gene-Disease Associations genes associated with the neonatal short-limb short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
prolonged neonatal jaundice Gene Set From HPO Gene-Disease Associations genes associated with the prolonged neonatal jaundice phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal hypoglycemia Gene Set From HPO Gene-Disease Associations genes associated with the neonatal hypoglycemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal onset Gene Set From HPO Gene-Disease Associations genes associated with the neonatal onset phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Neonatal Abstinence Syndrome Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Neonatal Abstinence Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Jaundice, Neonatal Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Jaundice, Neonatal 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.
Hyperbilirubinemia, Neonatal Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hyperbilirubinemia, Neonatal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Thrombocytopenia, Neonatal Alloimmune Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Thrombocytopenia, Neonatal Alloimmune phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
partial neonatal lethality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the partial neonatal lethality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
complete neonatal lethality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the complete neonatal lethality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
neonatal lethality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the neonatal lethality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
diabetes mellitus, neonatal, with congenital hypothyroidism Gene Set From OMIM Gene-Disease Associations genes associated with the diabetes mellitus, neonatal, with congenital hypothyroidism phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign neonatal, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign neonatal, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperparathyroidism, neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the hyperparathyroidism, neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
?diabetes mellitus, insulin-dependent, neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the ?diabetes mellitus, insulin-dependent, neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
diabetes mellitus, transient neonatal 2 Gene Set From OMIM Gene-Disease Associations genes associated with the diabetes mellitus, transient neonatal 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
rigidity and multifocal seizure syndrome, lethal neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the rigidity and multifocal seizure syndrome, lethal neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign neonatal, type 2 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign neonatal, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
?inflammatory skin and bowel disease, neonatal, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ?inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
?inflammatory skin and bowel disease, neonatal, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the ?inflammatory skin and bowel disease, neonatal, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
anemia, neonatal hemolytic, fatal and near-fatal Gene Set From OMIM Gene-Disease Associations genes associated with the anemia, neonatal hemolytic, fatal and near-fatal phenotype from the curated OMIM Gene-Disease Associations dataset.
thrombocytopenia, neonatal alloimmune Gene Set From OMIM Gene-Disease Associations genes associated with the thrombocytopenia, neonatal alloimmune phenotype from the curated OMIM Gene-Disease Associations dataset.
diabetes mellitus, permanent neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the diabetes mellitus, permanent neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperbilirubinemia, familial transient neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the hyperbilirubinemia, familial transient neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
myasthenia gravis, neonatal transient Gene Set From OMIM Gene-Disease Associations genes associated with the myasthenia gravis, neonatal transient phenotype from the curated OMIM Gene-Disease Associations dataset.
cpt ii deficiency, lethal neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the cpt ii deficiency, lethal neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
{diabetes mellitus, transient neonatal} Gene Set From OMIM Gene-Disease Associations genes associated with the {diabetes mellitus, transient neonatal} phenotype from the curated OMIM Gene-Disease Associations dataset.
neutropenia, neonatal alloimmune Gene Set From OMIM Gene-Disease Associations genes associated with the neutropenia, neonatal alloimmune phenotype from the curated OMIM Gene-Disease Associations dataset.
encephalopathy, neonatal severe Gene Set From OMIM Gene-Disease Associations genes associated with the encephalopathy, neonatal severe phenotype from the curated OMIM Gene-Disease Associations dataset.
thrombocytopenia, neonatal alloimmune, bak antigen related Gene Set From OMIM Gene-Disease Associations genes associated with the thrombocytopenia, neonatal alloimmune, bak antigen related phenotype from the curated OMIM Gene-Disease Associations dataset.
diabetes mellitus, transient neonatal, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the diabetes mellitus, transient neonatal, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
diabetes mellitus, transient neonatal, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the diabetes mellitus, transient neonatal, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
diabetes, permanent neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the diabetes, permanent neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
citrullinemia, type ii, neonatal-onset Gene Set From OMIM Gene-Disease Associations genes associated with the citrullinemia, type ii, neonatal-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
diabetes mellitus, permanent neonatal, with neurologic features Gene Set From OMIM Gene-Disease Associations genes associated with the diabetes mellitus, permanent neonatal, with neurologic features phenotype from the curated OMIM Gene-Disease Associations dataset.
choreoathetosis, hypothyroidism, and neonatal respiratory distress Gene Set From OMIM Gene-Disease Associations genes associated with the choreoathetosis, hypothyroidism, and neonatal respiratory distress phenotype from the curated OMIM Gene-Disease Associations dataset.
{hypertrypsinemia, neonatal} Gene Set From OMIM Gene-Disease Associations genes associated with the {hypertrypsinemia, neonatal} phenotype from the curated OMIM Gene-Disease Associations dataset.
neutropenia, alloimmune neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the neutropenia, alloimmune neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
{pulmonary hypertension, neonatal, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {pulmonary hypertension, neonatal, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
zinc deficiency, transient neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the zinc deficiency, transient neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
cyanosis, transient neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the cyanosis, transient neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
neonatal Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term neonatal in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
Neonatal Hypotonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Respiratory Failure Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Respiratory Failure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hyperbilirubinemia, Neonatal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hyperbilirubinemia, Neonatal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Abstinence Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Abstinence Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Hepatitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hepatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental Delay, Epilepsy, And Neonatal Diabetes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental Delay, Epilepsy, And Neonatal Diabetes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
K Atp Permanent Neonatal Diabetes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease K Atp Permanent Neonatal Diabetes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Diabetes Mellitus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Diabetes Mellitus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Hypoglycemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hypoglycemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Transient Neonatal Diabetes Mellitus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Transient Neonatal Diabetes Mellitus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adrenoleukodystrophy, Neonatal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adrenoleukodystrophy, Neonatal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Alloimmune Thrombocytopenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Alloimmune Thrombocytopenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sclerosing Cholangitis, Neonatal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sclerosing Cholangitis, Neonatal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Herpes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Herpes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Opiate Withdrawal Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Opiate Withdrawal Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Deformity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Deformity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Hypoxic Ischemic Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hypoxic Ischemic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Inflammatory Skin And Bowel Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Inflammatory Skin And Bowel Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Citrullinemia, Type Ii, Neonatal-Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Citrullinemia, Type Ii, Neonatal-Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Hemochromatosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hemochromatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Encephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rigidity And Multifocal Seizure Syndrome, Lethal Neonatal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rigidity And Multifocal Seizure Syndrome, Lethal Neonatal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Benign Neonatal Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Benign Neonatal Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Hypocalcemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hypocalcemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Pneumonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Systemic Lupus Erythematosus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Systemic Lupus Erythematosus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Transient Neonatal Renal Tubular Acidosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Transient Neonatal Renal Tubular Acidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Hyperparathyroidism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hyperparathyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Chlamydial Conjunctivitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Chlamydial Conjunctivitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Early-Onset Sepsis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Early-Onset Sepsis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Alloimmune Neonatal Neutropenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Alloimmune Neonatal Neutropenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Thrombocytopenia (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Thrombocytopenia (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Meningitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Meningitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Hyperglycemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hyperglycemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late Onset Neonatal Pneumonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late Onset Neonatal Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Late-Onset Sepsis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Late-Onset Sepsis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Torulopsis Glabrata Fungemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Torulopsis Glabrata Fungemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Marfan Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Marfan Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Diarrhea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Diarrhea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Intestinal Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Intestinal Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Noninfective Neonatal Diarrhea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Noninfective Neonatal Diarrhea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Necrotizing Enterocolitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Necrotizing Enterocolitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Respiratory System Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Respiratory System Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Leukaemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Leukaemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Hemolytic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hemolytic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Transient Neonatal Hypothyroidism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Transient Neonatal Hypothyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cyanosis, Transient Neonatal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cyanosis, Transient Neonatal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Indirect Hyperbilirubinemia, Neonatal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Indirect Hyperbilirubinemia, Neonatal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Alloimmune Thrombocytopenia (Nait) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Alloimmune Thrombocytopenia (Nait) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neonatal Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neonatal Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Maladjustment Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Maladjustment Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Neonatal Epilepsy, Nonfamilial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Neonatal Epilepsy, Nonfamilial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Listeriosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Listeriosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Neonatal Lactic Acidosis Due To Nfs1-Isd11 Complex Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Neonatal Lactic Acidosis Due To Nfs1-Isd11 Complex Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Thrombosis Of Cerebral Venous Sinus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Thrombosis Of Cerebral Venous Sinus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Unconjugated Hyperbilirubinemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Unconjugated Hyperbilirubinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
6Q24-Related Transient Neonatal Diabetes Mellitus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease 6Q24-Related Transient Neonatal Diabetes Mellitus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Rickets Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Rickets in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Testicular Torsion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Testicular Torsion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Laryngospasm, Severe Neonatal Episodic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Laryngospasm, Severe Neonatal Episodic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Zinc Deficiency, Neonatal, Due To Low Breast Milk Zinc Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Zinc Deficiency, Neonatal, Due To Low Breast Milk Zinc in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Disorder Of Endocrine System Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Disorder Of Endocrine System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Hyperthyroidism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hyperthyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Thyrotoxicosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Thyrotoxicosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Prolonged Neonatal Jaundice Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Prolonged Neonatal Jaundice in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Respiratory Distress Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Respiratory Distress in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Insulin-Dependent Diabetes Mellitus Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Insulin-Dependent Diabetes Mellitus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Jaundice Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Jaundice in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Onset Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Tremor, Neonatal Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tremor, Neonatal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Spontaneous Neonatal Pneumothorax Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spontaneous Neonatal Pneumothorax in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Neonatal Hypotonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Neonatal Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Breathing Dysregulation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Breathing Dysregulation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Cholestatic Liver Disease Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Cholestatic Liver Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Wrinkled Skin Of Hands And Feet Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Wrinkled Skin Of Hands And Feet in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Death Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Death in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hypertrypsinemia, Neonatal, Susceptibility To Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hypertrypsinemia, Neonatal, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Short-Limb Short Stature Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Short-Limb Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Short-Trunk Short Stature Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Short-Trunk Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Direct Hyperbilirubinemia, Neonatal Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Direct Hyperbilirubinemia, Neonatal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Inspiratory Stridor Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Inspiratory Stridor in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neonatal Epiphyseal Stippling Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neonatal Epiphyseal Stippling in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Transient Neonatal Hyperparathyroidism Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Transient Neonatal Hyperparathyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
neonatal lethality, complete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the neonatal lethality, complete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
neonatal lethality, incomplete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the neonatal lethality, incomplete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
neonatal lethality Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the neonatal lethality phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Neonatal astrocyte_Brain_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Neonatal astrocyte_Brain_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Benign neonatal seizures Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Benign neonatal seizures from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Neonatal period electroclinical syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Neonatal period electroclinical syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Neonatal diabetes Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Neonatal diabetes from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Permanent neonatal diabetes mellitus Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Permanent neonatal diabetes mellitus from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Neonatal diabetes Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal diabetes in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal respiratory failure Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal respiratory failure in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Permanent neonatal diabetes mellitus Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Permanent neonatal diabetes mellitus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal jaundice Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal jaundice in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal period electroclinical syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal period electroclinical syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Transient neonatal diabetes mellitus Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Transient neonatal diabetes mellitus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
neonatal-onset type II citrullinemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease neonatal-onset type II citrullinemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign neonatal seizures Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign neonatal seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal abstinence syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal abstinence syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal leukemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal thyrotoxicosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal thyrotoxicosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign familial neonatal epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 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 2025 dataset.
Transient neonatal thrombocytopenia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Transient neonatal thrombocytopenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Transient neonatal neutropenia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Transient neonatal neutropenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal myasthenia gravis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal myasthenia gravis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal candidiasis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal candidiasis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal diabetes mellitus with congenital hypothyroidism Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal diabetes mellitus with congenital hypothyroidism in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal infective mastitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal infective mastitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal intrahepatic cholestasis due to citrin deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal intrahepatic cholestasis due to citrin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal/infantile epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal/infantile epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal severe primary hyperparathyroidism Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal severe primary hyperparathyroidism phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Permanent neonatal diabetes mellitus Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Permanent neonatal diabetes mellitus phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal insulin-dependent diabetes mellitus Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal insulin-dependent diabetes mellitus phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal diabetes mellitus Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal diabetes mellitus phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Transitory neonatal diabetes mellitus Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Transitory neonatal diabetes mellitus phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Transient Neonatal Diabetes Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Transient Neonatal Diabetes phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe neonatal-onset encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe neonatal-onset encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
History of neonatal hypotonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the History of neonatal hypotonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal Marfan syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal Marfan syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign neonatal seizures Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign neonatal seizures phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign Neonatal Epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign Neonatal Epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal pseudo-hydrocephalic progeroid syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal pseudo-hydrocephalic progeroid syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal-onset encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal-onset encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal hypotonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal hypotonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal hypoglycemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal hypoglycemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated neonatal sclerosing cholangitis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated neonatal sclerosing cholangitis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal ichthyosis-sclerosing cholangitis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal ichthyosis-sclerosing cholangitis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal seizure Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal seizure phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Fetal and neonatal alloimmune thrombocytopenia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fetal and neonatal alloimmune thrombocytopenia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal death Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal death phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal respiratory distress Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal respiratory distress phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal inflammatory skin and bowel disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal inflammatory skin and bowel disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal white matter microstructure Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neonatal white matter microstructure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Neonatal total 25-hydroxyvitamin D levels (maternal genetic effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neonatal total 25-hydroxyvitamin D levels (maternal genetic effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Neonatal total 25-hydroxyvitamin D levels (fetal genetic effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neonatal total 25-hydroxyvitamin D levels (fetal genetic effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Neonatal cytokine/chemokine levels (maternal genetic effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neonatal cytokine/chemokine levels (maternal genetic effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Neonatal cytokine/chemokine levels (fetal genetic effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neonatal cytokine/chemokine levels (fetal genetic effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Neonatal lupus Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neonatal lupus phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 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.
Stroke Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Stroke from the curated CTD Gene-Disease Associations dataset.
Heat Stroke Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Heat Stroke from the curated CTD Gene-Disease Associations dataset.
Stroke Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Stroke in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
apoplexy; stroke; thrombotic microangiopathies; vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; stroke; thrombotic microangiopathies; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ischemia; myocardial infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease ischemia; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ischemia; myocardial infarction; stroke; revascularization, urgent Gene Set From GAD Gene-Disease Associations genes associated with the disease ischemia; myocardial infarction; stroke; revascularization, urgent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; hyperhomocysteinemia; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; hyperhomocysteinemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; carotid artery stenosis; carotid stenosis; hyperhomocysteinemia; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; carotid artery stenosis; carotid stenosis; hyperhomocysteinemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; pulmonary embolism; pulmonary embolisms; stroke; thrombosis; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; pulmonary embolism; pulmonary embolisms; stroke; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stroke; oxidative stress Gene Set From GAD Gene-Disease Associations genes associated with the disease stroke; oxidative stress in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
angina pectoris; apoplexy; myocardial infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease angina pectoris; apoplexy; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; foramen ovale, patent; stroke; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; foramen ovale, patent; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; peripheral vascular diseases; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; peripheral vascular diseases; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, sickle cell; apoplexy; sickle cell anemia; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, sickle cell; apoplexy; sickle cell anemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; sinus thrombosis, intracranial; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; sinus thrombosis, intracranial; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; recurrence; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; recurrence; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; heart diseases; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; heart diseases; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; stroke, lacunar; atherothrombotic brain infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; stroke, lacunar; atherothrombotic brain infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral infarct; stroke, lacunar Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral infarct; stroke, lacunar in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alpha-thalassemia; anemia, sickle cell; glucosephosphate dehydrogenase deficiency; hemolysis; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha-thalassemia; anemia, sickle cell; glucosephosphate dehydrogenase deficiency; hemolysis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; hyperhomocysteinemia; stroke; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; hyperhomocysteinemia; stroke; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; myocardial infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral hemorrhage; cerebral infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral hemorrhage; cerebral infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrial fibrillation; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease atrial fibrillation; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; intracranial arteriosclerosis; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; intracranial arteriosclerosis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; hypertension; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; ischemic attack, transient; stroke; transient ischemic attack Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; ischemic attack, transient; stroke; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarct stroke, ischemic Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarct stroke, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carotid artery diseases; cerebrovascular disorders; stroke; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease carotid artery diseases; cerebrovascular disorders; stroke; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; cerebral infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; cerebral infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; pregnancy complications, cardiovascular; premature birth; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; pregnancy complications, cardiovascular; premature birth; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dementia; memory disorders; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease dementia; memory disorders; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; hyperhomocysteinemia; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; hyperhomocysteinemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; atherosclerosis; brain ischemia; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; atherosclerosis; brain ischemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; coronary disease; coronary heart disease; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arterial occlusive diseases; brain infarction; brain ischemia; coronary artery disease; stroke; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease arterial occlusive diseases; brain infarction; brain ischemia; coronary artery disease; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ischemia; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease ischemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; carotid artery stenosis; carotid stenosis; infarction, middle cerebral artery; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; carotid artery stenosis; carotid stenosis; infarction, middle cerebral artery; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; cerebral hemorrhage; cerebral hemorrhages; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; cerebral hemorrhage; cerebral hemorrhages; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarction; stroke, ischemic Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarction; stroke, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain damage, chronic; hypertension; myocardial ischemia; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease brain damage, chronic; hypertension; myocardial ischemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; coronary artery disease; stroke; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; coronary artery disease; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; myocardial infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; inflammation; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; inflammation; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
intracranial aneurysm; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease intracranial aneurysm; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
foramen ovale, patent; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease foramen ovale, patent; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarction and stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarction and stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; stroke; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; stroke; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stroke, lacunar; leukoencephalopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease stroke, lacunar; leukoencephalopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarction; stroke; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarction; stroke; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; cardiovascular diseases; ischemia; stroke; vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; cardiovascular diseases; ischemia; stroke; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
migraine disorders; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease migraine disorders; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus; hypertension; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarct; thromboembolism, venous; c-reactive protein; stroke, ischemic Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarct; thromboembolism, venous; c-reactive protein; stroke, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial ischemia; nervous system diseases; postoperative complications; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial ischemia; nervous system diseases; postoperative complications; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; carotid artery diseases; hemochromatosis; hypertension; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; carotid artery diseases; hemochromatosis; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrial fibrillation; brain ischemia; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease atrial fibrillation; brain ischemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; stroke; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperhomocysteinemia; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; hypertension; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; carotid artery diseases; hemochromatosis; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; carotid artery diseases; hemochromatosis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; migraine disorders; myocardial infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; migraine disorders; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; diabetes complications; hypertension; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; diabetes complications; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; intracranial thrombosis; ischemic attack, transient; migraine disorders; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; intracranial thrombosis; ischemic attack, transient; migraine disorders; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus, type 2; inflammation; insulin resistance; metabolic syndrome x; myocardial infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; inflammation; insulin resistance; metabolic syndrome x; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; stroke; vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; stroke; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; myocardial infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; hypertension; osteoporosis; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; hypertension; osteoporosis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; intracranial arteriosclerosis; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; intracranial arteriosclerosis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; coronary disease; myocardial infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; coronary disease; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; multiple sclerosis; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; multiple sclerosis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral hemorrhage; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral hemorrhage; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; atherosclerosis; cerebral infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; atherosclerosis; cerebral infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain infarction; recurrence; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain infarction; recurrence; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; dyslipidemias; hypertension; metabolic syndrome x; obesity; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; dyslipidemias; hypertension; metabolic syndrome x; obesity; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; coronary disease; coronary heart disease; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; cardiovascular diseases; hypertension; myocardial ischemia; pulmonary embolism; stroke; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; cardiovascular diseases; hypertension; myocardial ischemia; pulmonary embolism; stroke; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; intracranial arterial diseases; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; intracranial arterial diseases; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis, coronary; stroke; adiponectin Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis, coronary; stroke; adiponectin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; atrial septal defects; brain ischemia; diabetes mellitus; heart septal defects, atrial; hypertension; intracranial thrombosis; ischemic attack, transient; stroke; transient ischemic attack Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; atrial septal defects; brain ischemia; diabetes mellitus; heart septal defects, atrial; hypertension; intracranial thrombosis; ischemic attack, transient; stroke; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypoxia-ischemia, brain; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease hypoxia-ischemia, brain; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stroke, lacunar Gene Set From GAD Gene-Disease Associations genes associated with the disease stroke, lacunar in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarction; stroke; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarction; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarct; stroke; angina; peripheral vascular disease Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarct; stroke; angina; peripheral vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; carotid artery diseases; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; carotid artery diseases; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stroke; sickle cell anemia Gene Set From GAD Gene-Disease Associations genes associated with the disease stroke; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus, type 2; diabetic angiopathies; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; diabetic angiopathies; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
intracranial thrombosis; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease intracranial thrombosis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chlamydophila infections; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease chlamydophila infections; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; stroke; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; stroke; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; arterial occlusive diseases; atherosclerosis; brain ischemia; carotid artery diseases; embolism; ischemic attack, transient; stroke; transient ischemic attack Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; arterial occlusive diseases; atherosclerosis; brain ischemia; carotid artery diseases; embolism; ischemic attack, transient; stroke; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stroke, ischemic; cerebrovascular disease; thrombosis, arterial Gene Set From GAD Gene-Disease Associations genes associated with the disease stroke, ischemic; cerebrovascular disease; thrombosis, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemorrhagic and ischemic stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease hemorrhagic and ischemic stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dementia, vascular; inflammation; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease dementia, vascular; inflammation; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; cardiovascular diseases; coronary disease; coronary heart disease; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; cardiovascular diseases; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarction; pulmonary embolism; stroke; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarction; pulmonary embolism; stroke; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aphasia; brain ischemia; cardiovascular diseases; cerebral hemorrhage; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease aphasia; brain ischemia; cardiovascular diseases; cerebral hemorrhage; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; cadasil; migraine disorders; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; cadasil; migraine disorders; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aneurysm, ruptured; intracranial aneurysm; stroke; subarachnoid hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease aneurysm, ruptured; intracranial aneurysm; stroke; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetic angiopathies; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetic angiopathies; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemorrhagic stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease hemorrhagic stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; coronary disease; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; coronary disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperhomocysteinemia; malnutrition; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; malnutrition; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stroke, ischemic; atherosclerosis, carotid Gene Set From GAD Gene-Disease Associations genes associated with the disease stroke, ischemic; atherosclerosis, carotid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; atherosclerosis; inflammation; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; atherosclerosis; inflammation; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; coronary disease; inflammation; stroke; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; coronary disease; inflammation; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stroke; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease stroke; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; diabetes mellitus; intracranial arteriosclerosis; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; diabetes mellitus; intracranial arteriosclerosis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; diabetes mellitus type ii; diabetes mellitus, type 2; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; diabetes mellitus type ii; diabetes mellitus, type 2; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ischaemic stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease ischaemic stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cognitive impairment, vascular stroke, ischemic Gene Set From GAD Gene-Disease Associations genes associated with the disease cognitive impairment, vascular stroke, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; hyperhomocysteinemia; intracranial arterial diseases; sinus thrombosis, intracranial; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; hyperhomocysteinemia; intracranial arterial diseases; sinus thrombosis, intracranial; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; cerebral hemorrhage; cerebral hemorrhages; ischemia; stroke; subarachnoid hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; cerebral hemorrhage; cerebral hemorrhages; ischemia; stroke; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholesterol, hdl; blood pressure, arterial; stroke; longevity Gene Set From GAD Gene-Disease Associations genes associated with the disease cholesterol, hdl; blood pressure, arterial; stroke; longevity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; intracranial hemorrhages; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; intracranial hemorrhages; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; cardiovascular diseases; myocardial infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; cardiovascular diseases; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; atherosclerosis; carotid artery diseases; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; atherosclerosis; carotid artery diseases; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
angina pectoris; apoplexy; cardiovascular diseases; diabetes mellitus; hyperlipidemias; hypertension; myocardial infarction; obesity; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease angina pectoris; apoplexy; cardiovascular diseases; diabetes mellitus; hyperlipidemias; hypertension; myocardial infarction; obesity; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, sickle cell; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, sickle cell; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stroke; thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease stroke; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; cerebral hemorrhage; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; cerebral hemorrhage; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; diabetes mellitus; hyperlipidemias; myocardial infarction; stroke; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; diabetes mellitus; hyperlipidemias; myocardial infarction; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; cardiovascular diseases; coronary restenosis; myocardial infarction; recurrence; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; cardiovascular diseases; coronary restenosis; myocardial infarction; recurrence; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obesity; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease obesity; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain infarction; brain ischemia; intracranial arteriosclerosis; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain infarction; brain ischemia; intracranial arteriosclerosis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; intracranial hemorrhages; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; intracranial hemorrhages; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; cerebral hemorrhage; cerebral hemorrhages; intracranial hemorrhages; stroke; subarachnoid hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; cerebral hemorrhage; cerebral hemorrhages; intracranial hemorrhages; stroke; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholesterol, hdl; triglycerides; cholesterol, ldl; cholesterol, total; glucose; stroke; carotid artery intima-media thickness Gene Set From GAD Gene-Disease Associations genes associated with the disease cholesterol, hdl; triglycerides; cholesterol, ldl; cholesterol, total; glucose; stroke; carotid artery intima-media thickness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anoxia; asphyxia; brain ischemia; disease models, animal; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease anoxia; asphyxia; brain ischemia; disease models, animal; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; carotid artery thrombosis; intracranial arteriosclerosis; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; carotid artery thrombosis; intracranial arteriosclerosis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; hypoxia-ischemia, brain; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; hypoxia-ischemia, brain; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; diabetes mellitus; hypertension; myocardial infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; diabetes mellitus; hypertension; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain hemorrhage; stroke, ischemic Gene Set From GAD Gene-Disease Associations genes associated with the disease brain hemorrhage; stroke, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; myocardial infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; ischemic attack, transient; stroke; thrombosis; transient ischemic attack Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; ischemic attack, transient; stroke; thrombosis; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stroke, lacunar; small-vessel disease Gene Set From GAD Gene-Disease Associations genes associated with the disease stroke, lacunar; small-vessel disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stroke; dementia Gene Set From GAD Gene-Disease Associations genes associated with the disease stroke; dementia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarct; hypertension; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarct; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; cerebral arterial diseases; intracranial embolism; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; cerebral arterial diseases; intracranial embolism; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; encephalitis; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; encephalitis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; atrial fibrillation; brain ischemia; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; atrial fibrillation; brain ischemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; atrial septal defects; heart septal defects, atrial; stroke; thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; atrial septal defects; heart septal defects, atrial; stroke; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; migraine disorders; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; migraine disorders; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aphasia; aphasia, nos; apoplexy; brain ischemia; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease aphasia; aphasia, nos; apoplexy; brain ischemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; coronary disease; coronary heart disease; stroke; venous thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; coronary disease; coronary heart disease; stroke; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis, coronary; stroke, ischemic Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis, coronary; stroke, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; inflammation; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; inflammation; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; coronary disease; myocardial infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; coronary disease; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; femur head necrosis; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; femur head necrosis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; diabetes mellitus; genetic diseases, inborn; hypertension; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; diabetes mellitus; genetic diseases, inborn; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; intracranial embolism and thrombosis; sinus thrombosis, intracranial; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; intracranial embolism and thrombosis; sinus thrombosis, intracranial; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; carotid artery diseases; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; carotid artery diseases; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; carotid artery, internal, dissection; hyperhomocysteinemia; stroke; vertebral artery dissection Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; carotid artery, internal, dissection; hyperhomocysteinemia; stroke; vertebral artery dissection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; cardiovascular diseases; carotid artery diseases; myocardial infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; cardiovascular diseases; carotid artery diseases; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
angina pectoris; ischemic attack, transient; lupus erythematosus, systemic; myocardial infarction; peripheral vascular diseases; stroke; vasculitis Gene Set From GAD Gene-Disease Associations genes associated with the disease angina pectoris; ischemic attack, transient; lupus erythematosus, systemic; myocardial infarction; peripheral vascular diseases; stroke; vasculitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; intracranial hemorrhages; myocardial infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; intracranial hemorrhages; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarct; stroke, atherothrombotic Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarct; stroke, atherothrombotic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; cerebral infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; cerebral infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; atrial fibrillation; embolism; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; atrial fibrillation; embolism; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; intracranial hemorrhages; myocardial infarction; stroke; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; intracranial hemorrhages; myocardial infarction; stroke; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; ischemic attack, transient; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; ischemic attack, transient; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; recurrence; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; recurrence; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; hypertension; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stroke; atherosclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease stroke; atherosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; cerebral hemorrhage; myocardial infarction; myocardial ischemia; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; cerebral hemorrhage; myocardial infarction; myocardial ischemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; myocardial infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; myocardial ischemia; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; myocardial ischemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stroke, ischemic; fibrinogen Gene Set From GAD Gene-Disease Associations genes associated with the disease stroke, ischemic; fibrinogen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; giant cell arteritis; polymyalgia rheumatica; stroke; temporal arteritis; vision, low Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; giant cell arteritis; polymyalgia rheumatica; stroke; temporal arteritis; vision, low in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; dementia, vascular; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; dementia, vascular; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; hypertension; myocardial infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; hypertension; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; atherosclerosis; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; atherosclerosis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; cerebral hemorrhage; cerebral hemorrhages; hypertension; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; cerebral hemorrhage; cerebral hemorrhages; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; cardiovascular diseases; coronary disease; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; cardiovascular diseases; coronary disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; hypertension; myocardial infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; hypertension; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stroke; fibrinogen Gene Set From GAD Gene-Disease Associations genes associated with the disease stroke; fibrinogen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; fabry disease; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; fabry disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; myocardial infarction; myocardial ischemia; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; myocardial infarction; myocardial ischemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; diabetes mellitus; dyslipidemias; hypertension; obesity; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; diabetes mellitus; dyslipidemias; hypertension; obesity; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; coronary artery disease; intracranial arteriosclerosis; myocardial infarction; stroke; vasculitis Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; coronary artery disease; intracranial arteriosclerosis; myocardial infarction; stroke; vasculitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
intracranial arteriosclerosis; ischemic attack, transient; myocardial infarction; recurrence; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease intracranial arteriosclerosis; ischemic attack, transient; myocardial infarction; recurrence; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stroke, hemorrhagic Gene Set From GAD Gene-Disease Associations genes associated with the disease stroke, hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; cerebrovascular accident; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; cerebrovascular accident; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; intracranial hemorrhages; stroke; subarachnoid hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; intracranial hemorrhages; stroke; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; dementia; myocardial infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; dementia; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; atrial septal defects; embolism, paradoxical; heart septal defects, atrial; migraine with aura; stroke; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; atrial septal defects; embolism, paradoxical; heart septal defects, atrial; migraine with aura; stroke; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; myocardial infarction; stroke; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; myocardial infarction; stroke; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; cerebrovascular disorders; ischemic attack, transient; recurrence; stroke; transient ischemic attack Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; cerebrovascular disorders; ischemic attack, transient; recurrence; stroke; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; cardiovascular diseases; ischemia; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; cardiovascular diseases; ischemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; cardiovascular diseases; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; cardiovascular diseases; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary heart disease; myocardial infarction; stroke; cerebrovascular disease Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary heart disease; myocardial infarction; stroke; cerebrovascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; cardiovascular diseases; coronary disease; peripheral vascular diseases; stroke; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; cardiovascular diseases; coronary disease; peripheral vascular diseases; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stroke, ischemic Gene Set From GAD Gene-Disease Associations genes associated with the disease stroke, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; coronary disease; coronary heart disease; myocardial infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; coronary disease; coronary heart disease; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; hyperlipidemias; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; hyperlipidemias; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; constriction, pathologic; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; constriction, pathologic; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; memory disorders; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; memory disorders; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; coronary artery disease; hyperhomocysteinemia; ischemic attack, transient; stroke; transient ischemic attack Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; coronary artery disease; hyperhomocysteinemia; ischemic attack, transient; stroke; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stroke, myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease stroke, myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; stroke, ischemic Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; stroke, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis, coronary; diabetes, type 2; lipids; stroke, ischemic Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis, coronary; diabetes, type 2; lipids; stroke, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral hemorrhage; recurrence; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral hemorrhage; recurrence; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; hyperhomocysteinemia; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; hyperhomocysteinemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; dyslipidemias; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; dyslipidemias; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
intracranial arteriosclerosis; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease intracranial arteriosclerosis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; chlamydophila infections; cytomegalovirus infections; enterovirus infections; herpesviridae infections; ischemia; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; chlamydophila infections; cytomegalovirus infections; enterovirus infections; herpesviridae infections; ischemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; myocardial infarction; peripheral vascular diseases; stroke; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; myocardial infarction; peripheral vascular diseases; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recurrence; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease recurrence; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; diabetic angiopathies; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; diabetic angiopathies; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; atherosclerosis; coronary disease; coronary heart disease; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; atherosclerosis; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; infarction, middle cerebral artery; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; infarction, middle cerebral artery; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies; stroke 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.
diabetes, type 2; stroke, ischemic Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes, type 2; stroke, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; hyperhomocysteinemia; ischemia; stroke; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; hyperhomocysteinemia; ischemia; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
metabolism disorders; myocardial infarction; stroke, ischemic Gene Set From GAD Gene-Disease Associations genes associated with the disease metabolism disorders; myocardial infarction; stroke, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ischemic stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease ischemic stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; cerebral arterial diseases; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; cerebral arterial diseases; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; intracranial hemorrhages; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; intracranial hemorrhages; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apnea; apoplexy; blood coagulation disorders; brain ischemia; cerebrovascular disorders; hypotony, muscle; muscle hypotonia; protein c deficiency; seizures; stroke; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease apnea; apoplexy; blood coagulation disorders; brain ischemia; cerebrovascular disorders; hypotony, muscle; muscle hypotonia; protein c deficiency; seizures; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarct; c-reactive protein; stroke, ischemic Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarct; c-reactive protein; stroke, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stroke, atherothrombotic Gene Set From GAD Gene-Disease Associations genes associated with the disease stroke, atherothrombotic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stroke Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term stroke in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
MELAS - Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes_Muscle - Striated (Skeletal) (MMHCC)_GSE1462 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during MELAS - Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes_Muscle - Striated (Skeletal) (MMHCC)_GSE1462 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Ischemic stroke Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Ischemic stroke phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Large artery stroke Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Large artery stroke phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Stroke (pediatric) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Stroke (pediatric) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Coronary artery disease or ischemic stroke Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Coronary artery disease or ischemic stroke phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Stroke Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Stroke phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Stroke (ischemic) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Stroke (ischemic) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Coronary artery disease or large artery stroke Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Coronary artery disease or large artery stroke phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
stroke Gene Set From GWASdb SNP-Phenotype Associations genes associated with the stroke phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
ischemic stroke Gene Set From GWASdb SNP-Phenotype Associations genes associated with the ischemic stroke phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
thromboembolic stroke Gene Set From HPO Gene-Disease Associations genes associated with the thromboembolic stroke phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
stroke-like episodes Gene Set From HPO Gene-Disease Associations genes associated with the stroke-like episodes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
stroke Gene Set From HPO Gene-Disease Associations genes associated with the stroke phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
ischemic stroke Gene Set From HPO Gene-Disease Associations genes associated with the ischemic stroke phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Stroke Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Stroke phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Heat Stroke Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Heat Stroke phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
decreased cardiac stroke volume Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cardiac stroke volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased cardiac stroke volume Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased cardiac stroke volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cardiac stroke volume Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cardiac stroke volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
{stroke, ischemic, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {stroke, ischemic, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{stroke, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {stroke, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{ischemic stroke, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {ischemic stroke, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{stroke, susceptibility to, 1} Gene Set From OMIM Gene-Disease Associations genes associated with the {stroke, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.
{stroke, hemorrhagic} Gene Set From OMIM Gene-Disease Associations genes associated with the {stroke, hemorrhagic} phenotype from the curated OMIM Gene-Disease Associations dataset.
Ischemic Stroke Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ischemic Stroke in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cardioembolic Stroke Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cardioembolic Stroke in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Post Stroke Depression Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Post Stroke Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myocardial Infarction, Stroke Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myocardial Infarction, Stroke in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Stroke Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Stroke in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thrombotic Stroke Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thrombotic Stroke in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Post Stroke Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Post Stroke Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Perinatal Arterial Ischemic Stroke Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Perinatal Arterial Ischemic Stroke in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Embolic Stroke Of Undetermined Source Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Embolic Stroke Of Undetermined Source in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Cord Stroke Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Cord Stroke in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Paralytic Stroke Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Paralytic Stroke in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Embolic Stroke Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Embolic Stroke in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Stroke Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Stroke in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Perinatal Stroke Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Perinatal Stroke in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Postoperative Stroke Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Postoperative Stroke in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Non-Alzheimer'S Dementia (E.G., Lewy Body Dementia, Vascular Or Multi-Infarct Dementia; Mixed Dementia; Frontotemporal Dementia Such As Pick'S Disease; And Dementia Related To Stroke, Parkinson'S Or Creutzfeldt-Jakob Diseases) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Non-Alzheimer'S Dementia (E.G., Lewy Body Dementia, Vascular Or Multi-Infarct Dementia; Mixed Dementia; Frontotemporal Dementia Such As Pick'S Disease; And Dementia Related To Stroke, Parkinson'S Or Creutzfeldt-Jakob Diseases) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mitochondrial Encephalopathy, Lactic Acidosis And Stroke-Like Episodes (Melas Syndrome) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mitochondrial Encephalopathy, Lactic Acidosis And Stroke-Like Episodes (Melas Syndrome) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Occlusive Stroke Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Occlusive Stroke in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Post Stroke Seizure Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Post Stroke Seizure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressing Stroke Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressing Stroke in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Post-Stroke Pain Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Post-Stroke Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Stroke Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Stroke in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Stroke, Ischemic, Susceptibility To Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Stroke, Ischemic, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
increased cardiac stroke volume Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased cardiac stroke volume phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased cardiac stroke volume Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cardiac stroke volume phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased cardiac stroke volume Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the increased cardiac stroke volume phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
decreased cardiac stroke volume Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the decreased cardiac stroke volume phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
Ischemic stroke Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ischemic stroke phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Stroke disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Stroke disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cardiovascular death, myocardial infarction or stroke in response to clopidogrel treatment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cardiovascular death, myocardial infarction or stroke in response to clopidogrel treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Stroke Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Stroke phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Postoperative stroke after cardiac surgery Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Postoperative stroke after cardiac surgery phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Early-onset ischemic stroke Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Early-onset ischemic stroke phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Acute ischemic stroke x type 2 diabetes interaction Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Acute ischemic stroke x type 2 diabetes interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Ischemic stroke Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Ischemic stroke phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Ischemic stroke (cardioembolic) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Ischemic stroke (cardioembolic) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Small vessel stroke Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Small vessel stroke phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
White matter hyperintensities in ischemic stroke Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White matter hyperintensities in ischemic stroke phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Ischemic stroke (large artery atherosclerosis) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Ischemic stroke (large artery atherosclerosis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Ischemic stroke (small artery occlusion) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Ischemic stroke (small artery occlusion) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Ischemic stroke (undetermined subtype) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Ischemic stroke (undetermined subtype) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
C-reactive protein levels in ischemic stroke Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the C-reactive protein levels in ischemic stroke phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Fibrinogen levels in ischemic stroke Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Fibrinogen levels in ischemic stroke phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Alzheimer's disease or small vessel stroke Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alzheimer's disease or small vessel stroke phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cardioembolic stroke (CCSp classification) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cardioembolic stroke (CCSp classification) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cardioembolic stroke (TOAST classification) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cardioembolic stroke (TOAST classification) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cardioembolic stroke (CCS and TOAST classification) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cardioembolic stroke (CCS and TOAST classification) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cardioembolic stroke (CCS or TOAST classification) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cardioembolic stroke (CCS or TOAST classification) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Large artery stroke (CCSp classification)j Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Large artery stroke (CCSp classification)j phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Large artery stroke (TOAST classification) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Large artery stroke (TOAST classification) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Large artery stroke (CCS and TOAST classification) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Large artery stroke (CCS and TOAST classification) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Large artery stroke (CCS or TOAST classification) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Large artery stroke (CCS or TOAST classification) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Small vessel stroke (CCSp classification) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Small vessel stroke (CCSp classification) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Small vessel stroke (CCS and TOAST classification) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Small vessel stroke (CCS and TOAST classification) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Small vessel stroke (CCS or TOAST classification) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Small vessel stroke (CCS or TOAST classification) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cardioembolic stroke (CCSc classification) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cardioembolic stroke (CCSc classification) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
3-month functional outcome in ischaemic stroke (modified Rankin score) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the 3-month functional outcome in ischaemic stroke (modified Rankin score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
3-month functional outcome in non-lacunar ischaemic stroke (modified Rankin score) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the 3-month functional outcome in non-lacunar ischaemic stroke (modified Rankin score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
3-month functional outcome in lacunar ischaemic stroke (modified Rankin score) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the 3-month functional outcome in lacunar ischaemic stroke (modified Rankin score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Lacunar stroke Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lacunar stroke phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Vitamin B levels in ischemic stroke Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Vitamin B levels in ischemic stroke phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Stroke (ischemic) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Stroke (ischemic) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Large artery stroke Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Large artery stroke phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Coronary artery disease or ischemic stroke Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Coronary artery disease or ischemic stroke phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Coronary artery disease or large artery stroke Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Coronary artery disease or large artery stroke phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Stroke (pediatric) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Stroke (pediatric) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
vWF levels in ischaemic stroke and hyperhomocysteinaemia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the vWF levels in ischaemic stroke and hyperhomocysteinaemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
PMC11176083-41588_2024_1755_MOESM7_ESM.xlsx-ExtFig2b_MI-Stroke-covariate_MITF Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC11176083-41588_2024_1755_MOESM7_ESM.xlsx-ExtFig2b_MI-Stroke-covariate_MITF transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.

Harmonizome 3.0

Neonatal Stroke Gene Set

encephalitis; glucosephosphate dehydrogenase deficiency; jaundice, neonatal; neonatal jaundice Gene Set

jaundice, neonatal; neonatal jaundice Gene Set

glucosephosphate dehydrogenase deficiency; hemolysis; jaundice, neonatal; neonatal jaundice Gene Set

cardiovascular disease; stroke; stroke, ischemic Gene Set

stroke, ischemic; stroke, hemorrhagic Gene Set

brain hemorrhage; stroke; stroke, lacunar Gene Set

Transient neonatal diabetes mellitus 1 Gene Set

Benign familial neonatal-infantile seizures Gene Set

Neonatal insulin-dependent diabetes mellitus Gene Set

Benign familial neonatal seizures 1 Gene Set

Benign familial neonatal seizures 2 Gene Set

Hyperparathyroidism, neonatal severe Gene Set

Inflammatory skin and bowel disease, neonatal, 2 Gene Set

Diabetes mellitus, permanent neonatal, with neurologic features Gene Set

Rigidity and multifocal seizure syndrome, lethal neonatal Gene Set

CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL Gene Set

Inflammatory skin and bowel disease, neonatal Gene Set

Neonatal adrenoleucodystrophy Gene Set

Permanent neonatal diabetes mellitus Gene Set

Neonatal intrahepatic cholestasis caused by citrin deficiency Gene Set

Diabetes mellitus, permanent neonatal, with cerebellar agenesis Gene Set

Cyanosis, transient neonatal Gene Set

Neonatal diabetes mellitus Gene Set

Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal Gene Set

Hyperparathyroidism, Neonatal Severe Primary Gene Set

Neonatal-onset citrullinemia type 2 Gene Set

Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress Gene Set

Diabetes Mellitus, Permanent Neonatal, with Cerebellar Agenesis Gene Set

Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene Set

Jaundice, Neonatal Gene Set

SEIZURES, BENIGN FAMILIAL NEONATAL, 2 Gene Set

Diabetes Mellitus, Transient Neonatal, 3 Gene Set

Diabetes Mellitus, Transient Neonatal, 1 Gene Set

Finnish lethal neonatal metabolic syndrome Gene Set

Diabetes Mellitus, Transient Neonatal, 2 Gene Set

Pancreatic beta cell agenesis with neonatal diabetes mellitus Gene Set

Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism Gene Set

Hyperbilirubinemia, Transient Familial Neonatal Gene Set

Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations Gene Set

Diabetes Mellitus, Permanent Neonatal Gene Set

Neonatal Abstinence Syndrome Gene Set

Epilepsy, Benign Neonatal Gene Set

Epilepsy, Benign Neonatal, 3 Gene Set

SEIZURES, BENIGN FAMILIAL NEONATAL, 1 Gene Set

Anemia, Neonatal Gene Set

Thrombocytopenia, Neonatal Alloimmune Gene Set

neonatal period electroclinical syndrome Gene Set

neonatal candidiasis Gene Set

neonatal anemia Gene Set

benign neonatal seizures Gene Set

neonatal leukemia Gene Set

neonatal diabetes mellitus Gene Set

transient neonatal neutropenia Gene Set

neonatal jaundice Gene Set

neonatal period electroclinical syndrome Gene Set

benign familial neonatal epilepsy Gene Set

neonatal thyrotoxicosis Gene Set

neonatal abstinence syndrome Gene Set

neonatal myasthenia gravis Gene Set

neonatal respiratory failure Gene Set

transient neonatal thrombocytopenia Gene Set

glucosephosphate dehydrogenase deficiency; hyperbilirubinemia, neonatal Gene Set

birth weight; hyperbilirubinemia, neonatal Gene Set

resp distress syndrome neonatal; respiratory distress syndrome, newborn Gene Set

hyperbilirubinemia, neonatal Gene Set

obstetric labor, premature; resp distress syndrome neonatal; respiratory distress syndrome, newborn; tachycardia Gene Set

bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections Gene Set

neonatal thrombocytopenia Gene Set

lung diseases; resp distress syndrome neonatal; respiratory distress syndrome, newborn Gene Set

bronchopulmonary dysplasia; respiratory distress syndrome, neonatal Gene Set

respiratory distress syndrome, neonatal Gene Set

meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders Gene Set

citrullinemia, adult-onset type ii; hepatitis, neonatal associated with cholestasis Gene Set

neonatal infection Gene Set

neonatal hyperbilirubinemia Gene Set

hyperbilirubinemia, neonatal; jaundice Gene Set

cutaneous neonatal lupus Gene Set

jaundice, neonatal Gene Set