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loading...| Preferred Name |
CREST Syndrome |
| 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#C193006 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C118468 |
| Contributing_Source |
NICHD mCode |
| DEFINITION |
A variant of systemic sclerosis characterized by calcinosis, Raynaud phenomenon, esophageal motility disorders, sclerodactyly, and telangiectasia. |
| FULL_SYN |
CREST Syndrome CR(E)ST syndrome lSSc Limited Cutaneous Systemic Sclerosis lcSSc Limited Cutaneous Systemic Scleroderma |
| label |
CREST Syndrome |
| Legacy Concept Name |
CREST_Syndrome |
| Preferred_Name |
CREST Syndrome |
| prefixIRI |
Thesaurus:C70646 |
| prefLabel |
CREST Syndrome |
| Semantic_Type |
Disease or Syndrome |
| UMLS_CUI |
C0206138 |
| subClassOf |
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