Brody myopathy MeSH Supplementary Concept Data 2025

Details
Concepts

MeSH Supplementary: Brody myopathy
Unique ID: C536607
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536607
Entry Term(s): Autosomal recessive Brody myopathy; Brody Disease
Registry Numbers: 0
Heading Mapped to: *Myotonia Congenita
Frequency: 13
Date of Entry: 2010/08/25
Revision Date: 2013/10/24

Brody myopathy Preferred

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