infarcts

Clear Filter

Results for "infarcts": 12 gene sets

Name
infarcts Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term infarcts in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
subcortical infarcts and leukoencephalopathy (cadasil)] Gene Set From GAD Gene-Disease Associations genes associated with the disease subcortical infarcts and leukoencephalopathy (cadasil)] in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
subcortical infarcts and leukoencephalopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease subcortical infarcts and leukoencephalopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
White matter hyperintensity volume in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the White matter hyperintensity volume in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
recurrent subcortical infarcts Gene Set From HPO Gene-Disease Associations genes associated with the recurrent subcortical infarcts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set From OMIM Gene-Disease Associations genes associated with the cerebral arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
Multiple Lacunar Infarcts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Lacunar Infarcts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Autosomal Recessive Arteriopathy With Subcortical Infarcts And Leukoencephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Autosomal Recessive Arteriopathy With Subcortical Infarcts And Leukoencephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Subcortical Infarcts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Subcortical Infarcts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent subcortical infarcts Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Recurrent subcortical infarcts phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.