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Nemaline myopathy 4 MeSH Supplementary Concept Data 2024


MeSH Supplementary
Nemaline myopathy 4
Unique ID
C538351
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C538351
Entry Term(s)
Cap Myopathy, Tpm2-Related
Nemaline myopathy caused by mutation in the tropomyosin 2 gene
Registry Number
0
Heading Mapped to
*Myopathies, Nemaline
Frequency
2
Date of Entry
2010/08/25
Revision Date
2012/11/05
Nemaline myopathy 4 Preferred
Cap Myopathy, Tpm2-Related Related
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