inclusion body myopathy, autosomal dominant

Preferred Label : inclusion body myopathy, autosomal dominant;

MeSH note : Autosomal dominant myopathy with congenital joint contractures, ophthalmoplegia, and rimmed vacuoles;

MeSH synonym : inclusion body myopathy 3;

Details

Origin ID

C538330;

UMLS CUI

C2931820;

Automatic exact mappings (from CISMeF team)
- inclusion body myositis [DO Concept]
- proximal myopathy and ophthalmoplegia [DO Concept]
MeSH term(s) associated for indexing
- contracture [MeSH Descriptor]
- myositis, inclusion body [MeSH Descriptor]
- ophthalmoplegia [MeSH Descriptor]
Record concept(s)
- Inclusion body myopathy, autosomal dominant [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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