FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term familial adult myoclonic epilepsy ID (Ontology) DOID:0111689 (Human Disease)
Definition An adolescence-adult electroclinical syndrome characterized by adult-onset cortical myoclonus typically first seen as tremulous finger movements and myoclonus of the extremities.
Also Known As "BAFME" ; "benign adult familial myoclonic epilepsy" ; "benign adult familial myoclonus epilepsy" (for all, see Synonyms field below)
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Data Class Field Records
Human Disease Models (FBhh)  DOID       1
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 Human Disease Models
 familial adult myoclonic epilepsy       1
Spanning Tree (Parents/Children)
Only view relationship:
  absence epilepsy
   |__adolescence-adult electroclinical syndrome
       |__familial adult myoclonic epilepsy  11 rec.
           |__familial adult myoclonic epilepsy 1 1 rec.
           |__familial adult myoclonic epilepsy 2 1 rec.
           |__familial adult myoclonic epilepsy 3 1 rec.
           |__familial adult myoclonic epilepsy 4 4 rec.
           |__familial adult myoclonic epilepsy 5 1 rec.
           |__familial adult myoclonic epilepsy 6 1 rec.
           |__familial adult myoclonic epilepsy 7 1 rec.
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Is a adolescence-adult electroclinical syndrome
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Synonyms
  • "BAFME" EXACT OMO:0003012
    "benign adult familial myoclonic epilepsy" EXACT
    "benign adult familial myoclonus epilepsy" EXACT
    "FAME" EXACT OMO:0003012
    "familial cortical myoclonic tremor and epilepsy" EXACT
    "FCMTE" EXACT OMO:0003012
Secondary IDs
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MIM:PS601068
ORDO:86814
SNOMEDCT_US_2023_03_01:717225001
UMLS_CUI:C4273988