epilepsy, myoclonic, benign adult familial, type 2

Preferred Label : epilepsy, myoclonic, benign adult familial, type 2;

MeSH synonym : BAFME2; epilepsy, familial adult myoclonic 2; FAME2; benign adult familial myoclonic epilepsy 2; cortical myoclonus and epilepsy, autosomal dominant;

Détails

Origin ID

C564313;

UMLS CUI

C1842852;

Currated CISMeF NLP mapping
- Epilepsy, familial adult myoclonic, 2 [OMIM Phenotype]
MeSH term(s) associated for indexing
- epilepsies, myoclonic [MeSH Descriptor]
Record concept(s)
- epilepsy, myoclonic, benign adult familial, type 2 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Benign adult familial myoclonic epilepsy [ORDO Disease]
- Epilepsy, familial adult myoclonic, 2 [OMIM Phenotype]
Validated automatic mappings to NTBT
- Benign adult familial myoclonic epilepsy [ORDO Disease]
- Benign adult familial myoclonic epilepsy (disorder) [SNOMED CT concept]

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