Jump to:
loading...| Preferred Name |
CREST Syndrome [Disease/Finding] |
|
| Synonyms |
Calcinosis, Raynaud's phenomenon, Esophageal dismobility, Sclerodactyly, Telangiectasia Syndrome |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000003618 |
|
| altLabel |
Calcinosis, Raynaud's phenomenon, Esophageal dismobility, Sclerodactyly, Telangiectasia Syndrome CREST Syndrome |
|
| cui |
C0206138 |
|
| MESH DEFINITION |
A mild form of LIMITED SCLERODERMA, a multi-system disorder. Its features include symptoms of CALCINOSIS; RAYNAUD DISEASE; ESOPHAGEAL MOTILITY DISORDERS; sclerodactyly, and TELANGIECTASIS. When the defect in esophageal function is not prominent, it is known as CRST syndrome. |
|
| MESH DUI |
D017675 |
|
| MeSH name |
CREST Syndrome |
|
| MESH UI |
M0026732 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000003618 |
|
| NUI |
N0000003618 |
|
| prefLabel |
CREST Syndrome [Disease/Finding] |
|
| SNOMED CID |
31848007 |
|
| tui |
T047 |
|
| subClassOf |
Create mapping