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Summary Literature (0)
DOID:0060751 - familial temporal lobe epilepsy 7

Disease Ontology Definition:A temporal lobe epilepsy characterized by autosomal dominant inheritance of focal seizures with prominent auditory symptoms and that has_material_basis_in heterozygous mutation in the RELN gene on chromosome 7q22.

Synonyms: ETL7

Xenbase Genes : reln

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014639 - frontal sulcus

MIM:
MIM:616436 - EPILEPSY, FAMILIAL TEMPORAL LOBE, 7; ETL7

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), temporal lobe epilepsy (is_a)