MeSH Browser

MeSH Supplementary: Myosclerosis, Autosomal Recessive
Unique ID: C564968
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564968
Entry Term(s): Myopathy, Myosclerotic; Myosclerosis, Congenital, of Lowenthal
Registry Numbers: 0
Heading Mapped to: *Myopathies, Structural, Congenital
Frequency: 1
Date Introduced: 2012/11/05
Last Updated: 2012/11/05

Myosclerosis, Autosomal Recessive MeSH Supplementary Concept Data 2026