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MIM:616461 - EPILEPSY, FAMILIAL TEMPORAL LOBE, 8; ETL8
Xenbase Genes: gal.1, gal.2
Human Disease Resource: OMIM
MONDO:0010898 - autosomal dominant epilepsy with auditory features |
MONDO:0014650 - familial temporal lobe epilepsy 8 |
DOID:0060754 - familial temporal lobe epilepsy 8 |