Deafness, Congenital, and Familial Myoclonic Epilepsy MeSH Supplementary Concept Data 2025

Details
Concepts

MeSH Supplementary: Deafness, Congenital, and Familial Myoclonic Epilepsy
Unique ID: C565649
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565649
Registry Numbers: 0
Heading Mapped to: Deafness / congenital; *Epilepsies, Myoclonic
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Deafness, Congenital, and Familial Myoclonic Epilepsy Preferred

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