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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,
Echinobase Genes :
MIM:614417 - epilepsy, familial temporal lobe, 5; etl5 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
temporal lobe epilepsy (is_a)