Cell Culture Ontology - Raynaud disease - Classes | NCBO BioPortal

Cell Culture Ontology

Last uploaded: July 23, 2014

Id	http://www.ebi.ac.uk/efo/EFO_1001145 http://www.ebi.ac.uk/efo/EFO_1001145
Preferred Name	Raynaud disease
Definitions	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	cold fingers, hereditary secondary Raynaud's phenomenon Raynaud syndrome Raynaud's syndrome (disorder) Raynaud's syndrome secondary Raynaud phenomenon Raynaud's syndrome NOS (disorder) Raynaud's syndrome (disorder) [ambiguous] secondary Raynaud disease Raynaud's disease (disorder) Raynaud Disease Raynaud's syndrome (disorder) [Ambiguous] Raynaud's disease secondary Raynaud's disease Raynaud disease See more See less
Type	http://www.w3.org/2002/07/owl#Class

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.
preferred label	Raynaud disease
label	Raynaud disease
prefLabel	Raynaud disease
database_cross_reference	MEDGEN:20473 MESH:D011928 NCIt:C50724 UMLS:C0034734 NCIT:C116359 MONDO:0008364 MeSH:D011928 ICD10CM:I73.0 SCTID:195295006 OMIM:179600 SNOMEDCT:195295006 DOID:10300 ICD9:443.0 See more See less
notation	EFO:1001145
in_subset	http://purl.obolibrary.org/obo/mondo/mondo-base#otar
term editor	Sirarat Sarntivijai
has_related_synonym	cold fingers, hereditary
id	EFO:1001145
gwas_trait	true
skos_exactMatch	http://purl.obolibrary.org/obo/EFO_1001145 http://linkedlifedata.com/resource/umls/id/C0034734 https://omim.org/entry/179600 http://purl.obolibrary.org/obo/NCIT_C116359 http://identifiers.org/snomedct/195295006 http://identifiers.org/mesh/D011928 http://purl.obolibrary.org/obo/DOID_10300 http://purl.bioontology.org/ontology/ICD10CM/I73.0 http://identifiers.org/medgen/20473 See more See less
subClassOf	http://www.ebi.ac.uk/efo/EFO_0003875 http://www.ebi.ac.uk/efo/EFO_0000508
type	http://www.w3.org/2002/07/owl#Class
has_exact_synonym	secondary Raynaud's phenomenon Raynaud syndrome Raynaud's syndrome (disorder) Raynaud's syndrome secondary Raynaud phenomenon Raynaud's syndrome NOS (disorder) Raynaud's syndrome (disorder) [ambiguous] secondary Raynaud disease Raynaud's disease (disorder) Raynaud Disease Raynaud's syndrome (disorder) [Ambiguous] Raynaud's disease secondary Raynaud's disease Raynaud disease See more See less

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