C206526Level 5
Susceptibility to Idiopathic Generalized Epilepsy-10
**Semantic type:** Finding
**Definition:** An autosomal dominant susceptibility to idiopathic generalized epilepsy-10, caused by mutation(s) in the GABRD gene, encoding gamma-aminobutyric acid receptor subunit delta. Mutations in the GABRD are also associated with susceptibility to idiopathic generalized epilepsy-10, generalized epilepsy with febrile seizures plus, type 5, and juvenile myoclonic epilepsy-7.
**Synonyms:** - EIG10
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