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Summary Literature (1)
MIM:600512 - EPILEPSY, FAMILIAL TEMPORAL LOBE, 1; ETL1

Xenbase Genes: lgi1, reln

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010898 - autosomal dominant epilepsy with auditory features
MONDO:0700090 - epilepsy, familial temporal lobe, 1

Disease Ontology (DO):
DOID:0060748 - familial temporal lobe epilepsy 1