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Medical Subject Headings
| Id | http://purl.bioontology.org/ontology/MESH/D003882
http://purl.bioontology.org/ontology/MESH/D003882
|
|---|---|
| Preferred Name | Dermatomyositis |
| Definitions |
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)
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| Synonyms |
Dermatomyositis, Adult Type
Juvenile Dermatomyositis
Adult Type Dermatomyositis
Dermatomyositis, Childhood Type
Dermatomyositis, Juvenile
Polymyositis Dermatomyositis
Childhood Type Dermatomyositis
Dermatopolymyositis
Juvenile Myositis
Polymyositis-Dermatomyositis
Myositis, Juvenile
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| 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) |
|---|---|
| altLabel |
Dermatomyositis, Adult Type
Juvenile Dermatomyositis
Adult Type Dermatomyositis
Dermatomyositis, Childhood Type
Dermatomyositis, Juvenile
Polymyositis Dermatomyositis
Childhood Type Dermatomyositis
Dermatopolymyositis
Juvenile Myositis
Polymyositis-Dermatomyositis
Myositis, Juvenile
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| prefLabel | Dermatomyositis
|
| Mapped from | |
| type | |
| tui | T047
|
| TERMUI |
T011553
T372463
T372462
T000922805
T372461
T372464
T000922806
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| TH |
NLM (2000)
NLM (1966)
NLM (2018)
ORD (2010)
|
| MMR | 20181010
|
| notation | D003882
|
| Inverse of RO | |
| Semantic type UMLS property | |
| Inverse of AQ |
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| DX | 19660101
|
| cui |
C0263666
C0221056
C0011633
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| DC | 1
|
| MN |
C05.651.594.819.500
C10.668.491.562.575.500
C17.800.185
C17.300.250
|
| AN | coordinate with PARANEOPLASTIC SYNDROMES if pertinent
|
| AQL | BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI
|
| MDA | 19990101
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| subClassOf |
| Delete | Subject | Author | Type | Created |
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