Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
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 - familial temporal lobe epilepsy 7

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