MeSH Browser

MeSH Supplementary: Myopathy, Congenital, With Fiber-Type Disproportion, X-Linked
Unique ID: C567594
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567594
Registry Numbers: 0
Heading Mapped to: *Myopathies, Structural, Congenital
Frequency: 0
Note: also known as CFTDX
Date of Entry: 2012/08/24
Revision Date: 2012/08/24

Myopathy, Congenital, With Fiber-Type Disproportion, X-Linked MeSH Supplementary Concept Data 2025