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Descriptor English: Raynaud Disease
Descriptor Spanish: Enfermedad de Raynaud
Descriptor enfermedad de Raynaud
Scope note: Trastorno vascular idiopático caracterizado por fenómeno de Raynaud bilateral, que consiste en palidez digital o CIANOSIS de instauración brusca, en respuesta a la exposición al frío o estrés.
Descriptor Portuguese: Doença de Raynaud
Descriptor French: Maladie de Raynaud
Entry term(s): Cold Fingers, Hereditary
Raynaud Phenomenon
Raynaud's Disease
Raynauds Disease
Tree number(s): C14.907.617.812
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D011928
Scope note: An idiopathic vascular disorder characterized by bilateral Raynaud phenomenon, the abrupt onset of digital paleness or CYANOSIS in response to cold exposure or stress.
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CN congenital
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Public MeSH Note: 2004; use RAYNAUD'S DISEASE 1966-2003
History Note: 2004 (1966)
Entry Version: RAYNAUD DIS
DeCS ID: 12362
Unique ID: D011928
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2004/01/01
Date of Entry: 1999/01/01
Revision Date: 2012/07/03
Raynaud Disease - Preferred
Concept UI M0018534
Scope note 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 term Raynaud Disease
Entry term(s) Cold Fingers, Hereditary
Raynaud's Disease
Raynauds Disease
Raynaud Phenomenon - Narrower
Concept UI M0449202
Preferred term Raynaud Phenomenon



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