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Inclusion Body Myopathy 3, Autosomal Dominant MeSH Supplementary Concept Data 2022


MeSH Supplementary
Inclusion Body Myopathy 3, Autosomal Dominant
Unique ID
C565311
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C565311
Entry Term(s)
Myopathy with Congenital Joint Contractures, Ophthalmoplegia, and Rimmed Vacuoles
Registry Number
0
Heading Mapped to
*Contracture
*Ophthalmoplegia
Myositis, Inclusion Body / *congenital
Frequency
1
Note
mutation in MYHC2A
Date of Entry
2012/11/05
Revision Date
2013/11/06
Inclusion Body Myopathy 3, Autosomal Dominant Preferred
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