familial adult myoclonic epilepsy 6
Ontology Term:
Status:
Live
Synonym:
BAFME6
FAME6
FCMTE6
benign adult familial myoclonic epilepsy 6
familial cortical myoclonic tremor and epilepsy 6
FAME6
FCMTE6
benign adult familial myoclonic epilepsy 6
familial cortical myoclonic tremor and epilepsy 6
Type:
Mapping to OMIM ID:
Comparative Info:
Learn more about this disease from studies in other model systems at the 
WormBase ID:
DOID:0111696
A familial adult myoclonic epilepsy that has_material_basis_in a heterozygous 5-bp repeat expansion in the TNRC6A gene on chromosome 16p12.1.
Child:
Associations based on experimental data:
Disease relevant gene:
Automatic gene association:
1 Inferred automatically: Inferred by orthology to human genes with OMIM annotation
