has material basis in germline mutation in RELN temporal lobe epilepsy familial temporal lobe epilepsy 7 https://www.malacards.org/card/epilepsy_familial_temporal_lobe_7 ETL7 UMLS:C4225327 DOID:0060751 epilepsy, familial temporal lobe, type 7 familial temporal lobe epilepsy type 7 MEDGEN:907609 OMIM:616436 GARD:0016112 epilepsy, familial temporal lobe, 7 MONDO:0014639 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.