MeSH Browser

MeSH Supplementary: Myopathy, Reducing Body, X-Linked, Childhood-Onset
Unique ID: C567468
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567468
Registry Number: 0
Heading Mapped to: Muscular Diseases / *congenital; *Genetic Diseases, X-Linked
Frequency: 2
Note: mutations in FHL1
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Myopathy, Reducing Body, X-Linked, Childhood-Onset MeSH Supplementary Concept Data 2024