MeSH Browser

MeSH Supplementary: Epilepsy, Myoclonic, Benign Adult Familial, Type 2
Unique ID: C564313
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564313
Entry Term(s): BAFME2; Benign Adult Familial Myoclonic Epilepsy 2; Cortical Myoclonus And Epilepsy, Autosomal Dominant; Epilepsy, Familial Adult Myoclonic 2; FAME2
Registry Numbers: 0
Heading Mapped to: *Epilepsies, Myoclonic
Frequency: 4
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Epilepsy, Myoclonic, Benign Adult Familial, Type 2 MeSH Supplementary Concept Data 2025