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Summary Literature (0)
MIM:616461 - EPILEPSY, FAMILIAL TEMPORAL LOBE, 8; ETL8

Xenbase Genes: gal.1, gal.2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010898 - autosomal dominant epilepsy with auditory features
MONDO:0014650 - familial temporal lobe epilepsy 8

Disease Ontology (DO):
DOID:0060754 - familial temporal lobe epilepsy 8