National Cancer Institute Thesaurus

Last uploaded: February 21, 2019

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#C118468 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C90259
Contributing_Source	NICHD
DEFINITION	A variant of systemic sclerosis characterized by calcinosis, Raynaud phenomenon, esophageal motility disorders, sclerodactyly, and telangiectasia.
FULL_SYN	Limited Cutaneous Systemic Scleroderma lcSSc Limited Cutaneous Systemic Sclerosis lSSc
Has_NICHD_Parent	http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C72070
label	CREST Syndrome
Legacy_Concept_Name	CREST_Syndrome
NICHD_Hierarchy_Term	Limited Cutaneous Systemic Sclerosis
Preferred_Name	CREST Syndrome
prefixIRI	C70646
prefLabel	CREST Syndrome
Semantic_Type	Disease or Syndrome
UMLS_CUI	C0206138
subClassOf	http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C28193

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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/DOID_0060218	Human Disease Ontology 123	LOOM
http://purl.bioontology.org/ontology/ICD10/M34.1	International Classification of Diseases, Version 10	LOOM
http://purl.bioontology.org/ontology/ICD10CM/M34.1	International Classification of Diseases, Version 10 - Clinical Modification	LOOM
http://purl.bioontology.org/ontology/MESH/D017675	Medical Subject Headings	LOOM