A temporal lobe epilepsy characterized by autosomal dominant inheritance of focal seizures with prominent auditory symptoms and that has material basis in heterozygous mutation in the RELN gene on chromosome 7q22. The disease is MONDO_0014639 (familial temporal lobe epilepsy 7). Also known as: ETL7, epilepsy, familial temporal lobe, type 7, familial temporal lobe epilepsy type 7.