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Summary Literature (0)
MIM:616436 - EPILEPSY, FAMILIAL TEMPORAL LOBE, 7; ETL7

Xenbase Genes: reln

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010898 - autosomal dominant epilepsy with auditory features
MONDO:0014639 - frontal sulcus

Disease Ontology (DO):
DOID:0060751 - familial temporal lobe epilepsy 7