DISEASES

Disease-gene associations mined from literature

Human genes for childhood absence epilepsy

Childhood absence epilepsy [DOID:1825]

A childhood electroclinical syndrome that is characterized by brief and frequent absence seizures in children with age of onset between four and ten years.

Synonyms:  childhood absence epilepsy,  childhood absence epilepsies,  DOID:1825,  petit mal seizure,  pyknolepsy ...