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;
Origin ID : C564313;
UMLS CUI : C1842852;
Currated CISMeF NLP mapping
MeSH term(s) associated for indexing
Record concept(s)
Semantic type(s)
UMLS correspondences (same concept)
Validated automatic mappings to NTBT
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=100010
2011
France
scientific and technical information
Epilepsy
adult
benin
epilepsy, myoclonic, benign adult familial, type 2
epilepsies, myoclonic
epilepsy, myoclonic, benign adult familial, type 2
adulthood
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