loading...| Preferred Name |
CREST Syndrome |
|
| Synonyms |
Limited Cutaneous Systemic Scleroderma Limited Cutaneous Systemic Sclerosis CREST Syndrome CR(E)ST syndrome lSSc lcSSc |
|
| Definitions |
A variant of systemic sclerosis characterized by calcinosis, Raynaud phenomenon, esophageal motility disorders, sclerodactyly, and telangiectasia. |
|
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C70646 |
|
| ALT_DEFINITION |
A variant of systemic scleroderma characterized by features such as calcinosis, Raynaud phenomenon, esophageal motility disorders, sclerodactyly, and telangiectasia. |
|
| code |
C70646 |
|
| Concept_In_Subset |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C118468 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C90259 |
|
| Contributing_Source |
NICHD mCode |
|
| DEFINITION |
A variant of systemic sclerosis characterized by calcinosis, Raynaud phenomenon, esophageal motility disorders, sclerodactyly, and telangiectasia. |
|
| FULL_SYN |
Limited Cutaneous Systemic Scleroderma Limited Cutaneous Systemic Sclerosis CREST Syndrome CR(E)ST syndrome lSSc lcSSc |
|
| label |
CREST Syndrome |
|
| Legacy Concept Name |
CREST_Syndrome |
|
| Preferred_Name |
CREST Syndrome |
|
| prefixIRI |
Thesaurus:C70646 |
|
| Semantic_Type |
Disease or Syndrome |
|
| UMLS_CUI |
C0206138 |
|
| subClassOf |