OBO ID: DOID:0111689
Term Name: familial adult myoclonic epilepsy Search Ontology:
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 )
OTHER familial adult myoclonic epilepsy PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None