C128189Level 11
Childhood Absence Epilepsy
**Semantic type:** Disease or Syndrome
**Definition:** A common generalized epilepsy syndrome occurring in children, characterized by absence seizures of short duration. The cause of the syndrome is presumed to be genetic. Genes which are associated with the condition include GABRB3, GABRG2, GABRA1, CACNA1H, and ECA1.
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