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Disease Ontology Browser
familial adult myoclonic epilepsy (DOID:0111689)
Alliance: disease page
Synonyms: BAFME; benign adult familial myoclonic epilepsy; benign adult familial myoclonus epilepsy; FAME; familial cortical myoclonic tremor and epilepsy; FCMTE
Alt IDs: OMIM:PS601068, ORDO:86814, UMLS_CUI:C4273988
Definition: An adolescence-adult electroclinical syndrome characterized by adult-onset cortical myoclonus typically first seen as tremulous finger movements and myoclonus of the extremities.


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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
08/02/2024
MGI 6.24
The Jackson Laboratory