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2014 MeSH

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Myositis, Inclusion Body
MeSH HeadingMyositis, Inclusion Body
Tree NumberC05.651.594.600
Tree NumberC10.668.491.562.500
Annotationdo not coord with INCLUSION BODIES but coord with INCLUSION BODIES, VIRAL if relevant (IM or NIM)
Scope NoteProgressive myopathies characterized by the presence of inclusion bodies on muscle biopsy. Sporadic and hereditary forms have been described. The sporadic form is an acquired, adult-onset inflammatory vacuolar myopathy affecting proximal and distal muscles. Familial forms usually begin in childhood and lack inflammatory changes. Both forms feature intracytoplasmic and intranuclear inclusions in muscle tissue. (Adams et al., Principles of Neurology, 6th ed, pp1409-10)
Entry TermInclusion Body Myopathy, Sporadic
Entry TermInclusion Body Myositis
Entry TermInclusion Body Myositis, Sporadic
Entry TermMyopathy, Inclusion Body, Sporadic
Entry TermMyositis, Inclusion Body, Sporadic
Entry TermSporadic Inclusion Body Myositis
Allowable QualifiersBL CF CI CL CN CO DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RA RH RI RT SU TH UR US VE VI
Previous Indexing Myositis (1968-1995)
History Note96
Date of Entry19950524
Unique IDD018979


MeSH Tree Structures

 
Musculoskeletal Diseases [C05]
   Muscular Diseases [C05.651]
      Myositis [C05.651.594]
Dermatomyositis [C05.651.594.297]
Arrow pointing to current tree nodeMyositis, Inclusion Body [C05.651.594.600]
Myositis Ossificans [C05.651.594.638]
Orbital Myositis [C05.651.594.728]
Polymyositis [C05.651.594.819]  +
Pyomyositis [C05.651.594.909]

 
Nervous System Diseases [C10]
   Neuromuscular Diseases [C10.668]
      Muscular Diseases [C10.668.491]
         Myositis [C10.668.491.562]
Dermatomyositis [C10.668.491.562.150]
Arrow pointing to current tree nodeMyositis, Inclusion Body [C10.668.491.562.500]
Orbital Myositis [C10.668.491.562.537]
Polymyositis [C10.668.491.562.575]  +
Pyomyositis [C10.668.491.562.787]

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