Preferred Name |
CREST Syndrome |
|
Synonyms |
|
|
Definitions |
A variant of systemic sclerosis characterized by calcinosis, Raynaud phenomenon, esophageal motility disorders, sclerodactyly, and telangiectasia. |
|
ID |
http://purl.obolibrary.org/obo/NCIT_C70646 |
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ALT_DEFINITION |
A variant of systemic scleroderma characterized by features such as calcinosis, Raynaud phenomenon, esophageal motility disorders, sclerodactyly, and telangiectasia. |
|
code |
C70646 |
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Contributing_Source |
NICHD |
|
definition |
A variant of systemic sclerosis characterized by calcinosis, Raynaud phenomenon, esophageal motility disorders, sclerodactyly, and telangiectasia. |
|
in_subset | ||
label |
CREST Syndrome |
|
Legacy Concept Name |
CREST_Syndrome |
|
Preferred_Name |
CREST Syndrome |
|
prefixIRI |
NCIT:C70646 |
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prefLabel |
CREST Syndrome |
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Semantic_Type |
Disease or Syndrome |
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UMLS_CUI |
C0206138 |
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subClassOf |
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