C179067Level 5
Susceptibility to Idiopathic Generalized Epilepsy-15
**Semantic type:** Finding
**Definition:** An autosomal dominant susceptibility to idiopathic generalized epilepsy-15, caused by mutation(s) in the RORB gene, encoding nuclear receptor ROR-beta. The condition is characterized by early-onset generalized seizures and may have associated developmental delay.
**Synonyms:** - EIG15
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