has material basis in germline mutation in LGI1 temporal lobe epilepsy autosomal dominant epilepsy with auditory features epilepsy, familial temporal lobe, 1 https://github.com/monarch-initiative/mondo/issues/1134 https://github.com/monarch-initiative/mondo/issues/2614 https://www.malacards.org/card/epilepsy_familial_temporal_lobe_1 epilepsy, lateral temporal lobe, autosomal dominant OMIM:600512 epilepsy, familial temporal lobe, type 1 MONDO:0700090 An autosomal dominant condition caused by mutation(s) in the LGI1 gene, encoding leucine-rich glioma-inactivated protein 1. It is characterized by partial seizures originating in the temporal lobe and often accompanied by auditory sensory manifestations. NCIT:C141441 ADLTE GARD:0026356 epilepsy, partial, with auditory features ADPEAF DOID:0060748 ETL1