Search Ontology:
Human Disease

familial adult myoclonic epilepsy

Term ID
DOID:0111689
Synonyms
  • ADCME
  • autosomal dominant cortical myoclonus and epilepsy
  • BAFME
  • benign adult familial myoclonic epilepsy
  • benign adult familial myoclonus epilepsy
  • FAME
  • familial cortical myoclonic tremor and epilepsy
  • FCMTE
Definition
An adolescence-adult electroclinical syndrome characterized by adult-onset cortical myoclonus typically first seen as tremulous finger movements and myoclonus of the extremities. https://www.ncbi.nlm.nih.gov/pubmed/20548044
References
  • OMIM:PS601068
  • ORDO:86814
  • SNOMEDCT_US_2023_03_01:717225001
  • UMLS_CUI:C4273988
Ontology
Human Disease   ( DOID:0111689 )
Relationships
is a type of
has subtype
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Genes Involved
Zebrafish Models
Citations