OBO ID: DOID:0060748 |
Term Name: | familial temporal lobe epilepsy 1 | Search Ontology: | |
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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) | ||
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Ontology: | Human Disease ( DOID:0060748 ) |
OTHER familial temporal lobe epilepsy 1 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS (1)
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