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EXPERIMENTAL FACTOR ONTOLOGY - ANNOTATIONS

Term:Raynaud disease
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Accession:EFO:1001145 term browser browse the term
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. An idiopathic vascular disorder characterized by bilateral Raynaud phenomenon, the abrupt onset of digital paleness or CYANOSIS in response to cold exposure or stress.
Synonyms:exact_synonym: DOID:10300;   NCIT:C116359;   Raynaud syndrome;   Raynaud's disease;   Raynaud's disease (disorder);   Raynaud's syndrome;   Raynaud's syndrome (disorder);   Raynaud's syndrome (disorder) [Ambiguous];   Raynaud's syndrome NOS (disorder);   http://identifiers.org/medgen/20473;   http://identifiers.org/mesh/D011928;   http://identifiers.org/snomedct/195295006;   http://linkedlifedata.com/resource/umls/id/C0034734;   http://purl.bioontology.org/ontology/ICD10CM/I73.0;   https://omim.org/entry/179600;   secondary Raynaud disease;   secondary Raynaud phenomenon;   secondary Raynaud's disease;   secondary Raynaud's phenomenon
 related_synonym: cold fingers, hereditary
 xref: DOID:10300;   ICD10CM:I73.0;   ICD9:443.0;   MEDGEN:20473;   MESH:D011928;   MIM:179600;   MONDO:0008364;   NCI:C116359;   NCI:C50724;   SCTID:195295006;   SNOMEDCT:195295006;   UMLS:C0034734


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                Raynaud disease 0
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