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Disease Ontology Browser
familial temporal lobe epilepsy 3 (DOID:0060750)
Alliance: disease page
Synonyms: familial mesial temporal lobe epilepsy; FMTLE
Alt IDs: OMIM:611630, ORDO:163717
Definition: A temporal lobe epilepsy characterized by simple or complex partial seizures often accompanied by intense feelings of deja or altered awareness and that has_material_basis_in variation in the chromosome region 4q13.2-q21.3.


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
03/19/2024
MGI 6.23
The Jackson Laboratory