MeSH Browser

MeSH Supplementary: Myopathy, Reducing Body, X-Linked, Early-Onset, Severe
Unique ID: C567469
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567469
Registry Numbers: 0
Heading Mapped to: Muscular Diseases / congenital; *Genetic Diseases, X-Linked
Frequency: 0
Note: mutations in FHL1
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Myopathy, Reducing Body, X-Linked, Early-Onset, Severe MeSH Supplementary Concept Data 2025