childhood absence epilepsy. Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A childhood electroclinical syndrome that is characterized by brief and frequent absence seizures in children with age of onset between four and ten years. (Human Disease Ontology, DOID_1825)
Similar Terms
Downloads & Tools

Genes

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

Symbol Name
CACNA1H calcium channel, voltage-dependent, T type, alpha 1H subunit