obsolete_dermatomyositis true true 3.88.0 Polydermatomyositis NCIt:C26744 Dermatomyositis, Adult Type DOID:10223 A subacute or chronic inflammatory disease of muscle and skin, marked by proximal muscle weakness and a characteristic skin rash. The illness occurs with approximately equal frequency in children and adults. The skin lesions usually take the form of a purplish rash (or less often an exfoliative dermatitis) involving the nose, cheeks, forehead, upper trunk, and arms. The disease is associated with a complement mediated intramuscular microangiopathy, leading to loss of capillaries, muscle ischemia, muscle-fiber necrosis, and perifascicular atrophy. The childhood form of this disease tends to evolve into a systemic vasculitis. Dermatomyositis may occur in association with malignant neoplasms. (From Adams et al., Principles of Neurology, 6th ed, pp1405-6) MESH:D003882 Dermatopolymyositis, unspecified (disorder) Dermatopolymyositis, unspecified Polymyositis Dermatomyositis http://purl.obolibrary.org/obo/MONDO_0016367 Polymyositis-Dermatomyositis [X]Dermatopolymyositis, unspecified (disorder) DM - Dermatomyositis Dermatomyositis (disorder) Adult Type Dermatomyositis Polymyositis with skin involvement Wagner-Unverricht syndrome James Malone ICD9:710.3 MedDRA:10012503 UMLS:C0011633 Dermatopolymyositis [X]Dermatopolymyositis, unspecified Dermatomyositides, Adult Type ICD10:M33 Gautier Koscielny Dermatomyositides Polymyositis-Dermatomyositides SNOMEDCT:396230008 Replaced by Mondo term MONDO_0016367, with which this term was previously merged. Use: http://purl.obolibrary.org/obo/MONDO_0016367 Dermatopolymyositides Adult Type Dermatomyositides A myositis and is_a dermatitis that results_in inflammation located_in muscle and located_in skin. The disease may result from either a viral infection or an autoimmune reaction. dermatopolymyositis Dermatomyositis, Childhood Type