|OBO ID: DOID:0060748|
|Term Name:||familial temporal lobe epilepsy 1||Search 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. (3)|
|Ontology:||Human Disease (DOID:0060748)|
|is a type of:||
OTHER familial temporal lobe epilepsy 1 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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