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Disease Ontology Browser
familial temporal lobe epilepsy 5 (DOID:0060752)
Alliance: disease page
Synonyms: ETL5
Alt IDs: OMIM:614417, ORDO:163717
Definition: A temporal lobe epilepsy that has_material_basis_in heterozygous mutation in the CPA6 gene on chromosome 8q13.

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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MGI 6.17
The Jackson Laboratory