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DOID:0060748 - familial temporal lobe epilepsy 1
Disease Ontology Definition:A temporal lobe epilepsy characterized by autosomal dominant inheritance of partial seizures originating from the temporal lobe that are often accompanied by auditory symptoms and that has_material_basis_in heterozygous mutation in the LGI1 gene on chromosome 10q24.
Synonyms: ETL1, partial epilepsy with auditory features,
Echinobase Genes :
MIM:600512 - epilepsy, familial temporal lobe, 1; etl1 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee