National Cancer Institute Thesaurus

Last uploaded: February 21, 2019
Preferred Name

Raynaud Phenomenon

ID

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C50724

ALT_DEFINITION

An episodic vasoconstriction resulting in discoloration of the skin and pain in the affected areas, often involving fingers or toes. Classically associated with triphasic color changes (white, blue, red) but may be biphasic. Often occurs in response to cold temperatures or emotional stress. May be primary or secondary to an underlying autoimmune disease.

Intermittent bilateral attacks of ischemia of the fingers or toes and sometimes of the ears or nose, marked by severe pallor, and often accompanied by paresthesia and pain.

code

C50724

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

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C54450

Contributing_Source

NICHD

FDA

DEFINITION

An episodic vasoconstriction resulting in discoloration of the skin and pain in the affected areas, often involving fingers or toes. Classically associated with triphasic color changes (white, blue, red) but may be biphasic. Often occurs in response to cold temperatures or emotional stress. May be primary or secondary to an underlying autoimmune disease.

FDA_Table

Patient Code (Appendix B)

FULL_SYN

Raynaud Disease

Phenomenon, Raynauds

Raynauds Phenomenon

Raynaud's Phenomenon

Raynaud's Disease

Has_CDRH_Parent

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C54027

Has_NICHD_Parent

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C35117

label

Raynaud Phenomenon

Legacy_Concept_Name

Raynauds_Syndrome

NICHD_Hierarchy_Term

Raynaud Phenomenon

Preferred_Name

Raynaud Phenomenon

prefixIRI

C50724

prefLabel

Raynaud Phenomenon

Semantic_Type

Disease or Syndrome

UMLS_CUI

C0034735

subClassOf

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C35136

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/MTHU025938 Online Mendelian Inheritance in Man LOOM
http://purl.obolibrary.org/obo/HP_0030880 Human Phenotype Ontology China LOOM
http://purl.bmicc.cn/ontology/ICD11CN/BD42 International Classification of Diseases, 11th Edition, China LOOM