OMOP Concept 37397175

Benign adult familial myoclonic epilepsy

StandardConditionSNOMED717225001Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2016
Valid to
31 Dec 2099
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Source codes that map to this concept

1 source code normalizes to Benign adult familial myoclonic epilepsy via the OMOP "Maps to" relationship.

VocabularyCodeNameType
Nebraska Lexicon717225001Autosomal dominant cortical myoclonus and epilepsyNon-standard

Synonyms

Alternative names recorded for Benign adult familial myoclonic epilepsy across source vocabularies.

  • Autosomal dominant cortical myoclonus and epilepsy
  • BAFME - Benign adult familial myoclonic epilepsy
  • Benign adult familial myoclonic epilepsy (disorder)
  • Benign adult familial myoclonus epilepsy
  • epilepsia mioclónica familiar benigna del adulto
  • epilepsia mioclónica familiar benigna del adulto (trastorno)

Where it sits in the hierarchy

Ordered by distance - 1 is a direct parent or child.

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