Preferred Name

Dermatomyositis [Disease/Finding]

Synonyms

Dermatomyositis

ID

http://purl.bioontology.org/ontology/NDFRT/N0000000946

altLabel

Dermatomyositis

Dermatopolymyositis

Polymyositis-Dermatomyositis

cui

C0011633

May be prevented by

http://purl.bioontology.org/ontology/NDFRT/N0000150783

http://purl.bioontology.org/ontology/NDFRT/N0000165176

http://purl.bioontology.org/ontology/NDFRT/N0000161732

http://purl.bioontology.org/ontology/NDFRT/N0000150778

http://purl.bioontology.org/ontology/NDFRT/N0000191518

http://purl.bioontology.org/ontology/NDFRT/N0000191516

http://purl.bioontology.org/ontology/NDFRT/N0000191517

http://purl.bioontology.org/ontology/NDFRT/N0000146229

http://purl.bioontology.org/ontology/NDFRT/N0000150776

http://purl.bioontology.org/ontology/NDFRT/N0000150772

http://purl.bioontology.org/ontology/NDFRT/N0000162834

http://purl.bioontology.org/ontology/NDFRT/N0000150774

http://purl.bioontology.org/ontology/NDFRT/N0000150773

http://purl.bioontology.org/ontology/NDFRT/N0000150777

http://purl.bioontology.org/ontology/NDFRT/N0000150775

http://purl.bioontology.org/ontology/NDFRT/N0000150784

http://purl.bioontology.org/ontology/NDFRT/N0000165177

http://purl.bioontology.org/ontology/NDFRT/N0000165175

May be treated by

http://purl.bioontology.org/ontology/NDFRT/N0000146744

http://purl.bioontology.org/ontology/NDFRT/N0000151453

http://purl.bioontology.org/ontology/NDFRT/N0000146286

http://purl.bioontology.org/ontology/NDFRT/N0000155587

http://purl.bioontology.org/ontology/NDFRT/N0000146387

http://purl.bioontology.org/ontology/NDFRT/N0000146287

MESH DEFINITION

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 DUI

D003882

MeSH name

Dermatomyositis

MESH UI

M0006061

NDFRT kind

DISEASE_KIND

notation

N0000000946

NUI

N0000000946

prefLabel

Dermatomyositis [Disease/Finding]

SNOMED CID

396230008

tui

T047

subClassOf

http://purl.bioontology.org/ontology/NDFRT/N0000000839

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