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inclusion body myositis

Disease Summary
Associated Targets (3)
Tbio

3


GARD Rare
Mondo Description Inclusion body myositis (IBM) is a slowly progressive degenerative inflammatory disorder of skeletal muscles characterized by late onset weakness of specific muscles and distinctive histopathological features.
Disease Ontology Description A myositis that is characterized by slowly progressive weakness and wasting of both distal and proximal muscles, most apparent in the muscles of the arms and legs that can occur in a sporadic or hereditary forms.
Mondo Term and Equivalent IDs
MONDO:0007827:  inclusion body myositis
COHD:4216406: 
EFO:0007323: 
GARD:0003896: 
ICD9:359.71: 
MESH:D018979: 
NCIT:C84786: 
Orphanet:611: 
SCTID:72315009: 
UMLS:C0238190: