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Summary Literature (0)
DOID:0060754 - familial temporal lobe epilepsy 8

Disease Ontology Definition:A temporal lobe epilepsy characterized by autosomal dominant inheritance of complex partial seizures with occasional secondary generalization and that has_material_basis_in heterozygous mutation in the GAL gene on chromosome 11q13.

Synonyms: ETL8

Xenbase Genes : gal.1, gal.2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014650 - familial temporal lobe epilepsy 8


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)