familial temporal lobe epilepsy 7 Disease Ontology Browser

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Disease Ontology Browser

familial temporal lobe epilepsy 7 (DOID:0060751)
Alliance: disease page
Synonyms: ETL7
Alt IDs: OMIM:616436, ORDO:101046
Definition: A temporal lobe epilepsy characterized by autosomal dominant inheritance of focal seizures with prominent auditory symptoms and that has_material_basis_in heterozygous mutation in the RELN gene on chromosome 7q22.

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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