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Disease Ontology Browser
familial adult myoclonic epilepsy 6 (DOID:0111696)
Alliance: disease page
Synonyms: BAFME6; benign adult familial myoclonic epilepsy 6; FAME6; familial cortical myoclonic tremor and epilepsy 6; FCMTE6
Alt IDs: OMIM:618074
Definition: A familial adult myoclonic epilepsy that has_material_basis_in a heterozygous 5-bp repeat expansion in the TNRC6A gene on chromosome 16p12.1.


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
04/16/2024
MGI 6.23
The Jackson Laboratory