Acquired idiopathic inflammatory myopathy

rare

An umbrella term for diseases which have chronic muscle inflammation and weakness of unknown etiology. The types of idiopathic inflammatory myopathy are further defined by either clinicopathologic criteria or by the presence of certain autoantibodies.

Identifiers: MONDO:0020122 Orphanet:98482
Part of: Acquired skeletal muscle disease Idiopathic disease Idiopathic inflammatory myopathy
Also known as: idiopathic inflammatory myopathies · idiopathic inflammatory myopathy, familial · idiopathic inflammatory myositis · IIm · IMM

Subtypes

All diseases Rare only

Disease	ID	Subtypes
Polymyositis	MONDO:0019127	15
Juvenile idiopathic inflammatory myopathy	MONDO:0018010	3
Antisynthetase syndrome	MONDO:0019344
Eosinophilic fasciitis	MONDO:0009175
Focal myositis	MONDO:0018845
Idiopathic eosinophilic myositis	MONDO:0016610
Immune-mediated necrotizing myopathy	MONDO:0016098
Inflammatory myopathy with abundant macrophages	MONDO:0016609
Overlap myositis	MONDO:0016099

Rare disease

Projects

Including projects on subtypes.

No projects yet.