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Inclusion body myopathy, autosomal dominant MeSH Supplementary Concept Data 2022


MeSH Supplementary
Inclusion body myopathy, autosomal dominant
Unique ID
C538330
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C538330
Entry Term(s)
Inclusion body myopathy 3
Registry Number
0
Heading Mapped to
Contracture / *congenital
*Ophthalmoplegia
Myositis, Inclusion Body / *congenital
Frequency
7
Note
Autosomal dominant myopathy with congenital joint contractures, ophthalmoplegia, and rimmed vacuoles
Date of Entry
2010/08/25
Revision Date
2013/11/06
Inclusion body myopathy, autosomal dominant Preferred
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