temporal lobe epilepsy autosomal dominant epilepsy with auditory features https://github.com/monarch-initiative/mondo/issues/1134 https://github.com/monarch-initiative/mondo/issues/2614 https://github.com/monarch-initiative/mondo/issues/8456 https://www.malacards.org/card/autosomal_dominant_epilepsy_with_auditory_features MONDO:0010898 partial epilepsy with auditory features UMLS:C1838062 ADEAF GARD:0002257 adolescent/adult onset autosomal dominant epilepsy with auditory features ADPEAF autosomal dominant partial epilepsy with auditory features Orphanet:101046 autosomal dominant epilepsy with auditory features autosomal dominant lateral temporal lobe epilepsy MESH:C537297 icd11.foundation:832717248 A rare, genetic, familial partial epilepsy disease characterized by focal seizures associated with prominent ictal auditory symptoms, and/or receptive aphasia, presenting in two or more family members and having a relatively benign evolution. MEDGEN:325326 partial epilepsy with auditory aura Autosomal dominant epilepsy with auditory features ADLTE autosomal dominant partial/lateral temporal epilepsy with auditory features familial partial epilepsy obsolete adolescent/adult-onset epilepsy syndrome epilepsy with auditory features