loading...| Preferred Name |
Myositis, Inclusion Body [Disease/Finding] |
|
| Synonyms |
Inclusion Body Myositis |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000003883 |
|
| altLabel |
Inclusion Body Myositis Myositis, Inclusion Body |
|
| cui |
C0238190 |
|
| MESH DEFINITION |
Progressive myopathies characterized by the presence of inclusion bodies on muscle biopsy. Sporadic and hereditary forms have been described. The sporadic form is an acquired, adult-onset inflammatory vacuolar myopathy affecting proximal and distal muscles. Familial forms usually begin in childhood and lack inflammatory changes. Both forms feature intracytoplasmic and intranuclear inclusions in muscle tissue. (Adams et al., Principles of Neurology, 6th ed, pp1409-10) |
|
| MESH DUI |
D018979 |
|
| MeSH name |
Myositis, Inclusion Body |
|
| MESH UI |
M0028350 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000003883 |
|
| NUI |
N0000003883 |
|
| prefLabel |
Myositis, Inclusion Body [Disease/Finding] |
|
| SNOMED CID |
72315009 |
|
| tui |
T047 |
|
| subClassOf |