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loading...| Preferred Name | Mixed Connective Tissue Disease [Disease/Finding] | |
| Synonyms |
Connective Tissue Disease, Mixed MCTD Sharp Syndrome Mixed Connective Tissue Disease |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000002022 |
|
| altLabel |
Connective Tissue Disease, Mixed MCTD Sharp Syndrome Mixed Connective Tissue Disease |
|
| cui |
C0026272 |
|
| MESH DEFINITION |
A syndrome with overlapping clinical features of systemic lupus erythematosus, scleroderma, polymyositis, and Raynaud's phenomenon. The disease is differentially characterized by high serum titers of antibodies to ribonuclease-sensitive extractable (saline soluble) nuclear antigen and a "speckled" epidermal nuclear staining pattern on direct immunofluorescence. |
|
| MESH DUI |
D008947 |
|
| MeSH name |
Mixed Connective Tissue Disease |
|
| MESH UI |
M0013961 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000002022 |
|
| NUI |
N0000002022 |
|
| prefLabel |
Mixed Connective Tissue Disease [Disease/Finding] |
|
| SNOMED CID |
398049005 398021003 |
|
| tui |
T047 |
|
| subClassOf |
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