MeSH Browser

MeSH Supplementary: Nemaline myopathy 5
Unique ID: C538397
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538397
Entry Term(s): Amish Nemaline Myopathy; Nemaline Myopathy, Amish Type; Nemaline myopathy, caused by mutation in the troponin t1 gene
Registry Numbers: 0
Heading Mapped to: *Myopathies, Nemaline
Frequency: 5
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Nemaline myopathy 5 MeSH Supplementary Concept Data 2025