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Disease Ontology Browser
familial temporal lobe epilepsy 1 (DOID:0060748)
Alliance: disease page
Synonyms: ETL1; partial epilepsy with auditory features
Alt IDs: OMIM:600512, ORDO:101046
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.

Disease References using Mouse Models (4)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
MGI 6.14
The Jackson Laboratory