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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease myositis
Comorbidity C0011633|dermatomyositis
Sentences 5
PubMedID- 25328739 Dermatomyositis (dm) is one of the idiopathic inflammatory myopathies caused by complement-mediated vasculopathy or vasculitis in the muscle.
PubMedID- 24587064 Polymyositis (pm), together with dermatomyositis, belongs to idiopathic inflammatory myositis, which represents a heterogeneous group of autoimmune systemic diseases characterized by chronic muscle weakness and inflammatory cell infiltrates in skeletal muscle [7].
PubMedID- 24288551 Dm (dermatomyositis) is a subtype of inflammatory myopathies, which is a rare autoimmune disease of skeletal muscle.
PubMedID- 22575417 Dermatomyositis (dm), one of autoimmune inflammatory myopathies, is characterized by inflammatory cell infiltration (cd4(+) t cells and b cells) in skeletal muscle.
PubMedID- 24615538 Polymyositis (pm) and dermatomyositis (dm), members of idiopathic inflammatory myopathies (iims), a group of systemic autoimmune diseases are also associated with elevated risk of cardiovascular diseases (cvd).

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