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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
myositis +     
antisynthetase syndrome  
Familial Idiopathic Inflammatory Myopathy  
fibromyalgia +   
granulomatous myositis 
inclusion body myositis +   
A myositis that is characterized by late onset of skeletal muscle inflammation, weakness, and atrophy with cytoplasmic granules and vacuoles in the muscle. (DO)
Macrophagic Myofasciitis 
myositis fibrosa 
myositis ossificans  
Orbital Myositis 
polymyositis +   
pyomyositis 
tendinitis +   

Synonyms
Exact Synonyms: HIBM ;   Hereditary Inclusion Body Myopathy ;   IBM ;   IBM-3 ;   Inclusion Body Myopathy, Sporadic ;   inclusion body myopathy 3 ;   inclusion body myositides ;   sporadic inclusion body myositis
Primary IDs: MESH:D018979
Alternate IDs: OMIM:147421
Xrefs: GARD:3896 ;   ICD10CM:G72.41 ;   ICD9CM:359.71 ;   NCI:C84786 ;   ORDO:611
Definition Sources: http://en.wikipedia.org/wiki/Inclusion_body_myositis "DO", https://ghr.nlm.nih.gov/condition/idiopathic-inflammatory-myopathy "DO"

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.