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Summary Literature (0)
DOID:0060752 - familial temporal lobe epilepsy 5

Disease Ontology Definition:A temporal lobe epilepsy that has_material_basis_in heterozygous mutation in the CPA6 gene on chromosome 8q13.

Synonyms: ETL5

Xenbase Genes : cpa6

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013741 - familial temporal lobe epilepsy 5

MIM:
MIM:614417 - EPILEPSY, FAMILIAL TEMPORAL LOBE, 5; ETL5

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), autosomal recessive disease (is_a), temporal lobe epilepsy (is_a)