MeSH Browser

MeSH Supplementary: Epilepsy, Benign Neonatal, Autosomal Recessive
Unique ID: C564823
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564823
Entry Term(s): Convulsions, Benign Familial Neonatal, Autosomal Recessive; Seizures, Benign Familial Neonatal, Autosomal Recessive
Registry Numbers: 0
Heading Mapped to: *Epilepsy, Benign Neonatal
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Epilepsy, Benign Neonatal, Autosomal Recessive MeSH Supplementary Concept Data 2025