MeSH Browser

MeSH Heading: von Willebrand Diseases
Tree Number(s): C15.378.100.100.900; C15.378.100.141.900; C15.378.140.900; C15.378.463.920; C16.320.099.920
Unique ID: D014842
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D014842
Annotation: note specific types of Von Willebrand Disease are available
Scope Note: Group of hemorrhagic disorders in which the VON WILLEBRAND FACTOR is either quantitatively or qualitatively abnormal. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor VIII, and impaired platelet adhesion.
Entry Term(s): Angiohemophilia; Hemophilia, Vascular; Vascular Pseudohemophilia; Von Willebrand Disorder; Von Willebrand's Factor Deficiency; von Willebrand Disease; von Willebrand Disease, Recessive Form; von Willebrand's Disease; von Willebrand's Diseases
NLM Classification #: WH 312
Public MeSH Note: 2010; see VON WILLEBRAND DISEASE 1999-2009; see VON WILLEBRAND'S DISEASE 1968-1998, see HEMORRHAGIC DIATHESIS 1967, see THROMBOCYTOPATHY 1963-1966
History Note: 2010(1963)
Date Established: 1968/01/01
Date of Entry: 1999/01/01
Revision Date: 2013/07/08

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Concept UI: M0022853
Scope Note: Group of hemorrhagic disorders in which the VON WILLEBRAND FACTOR is either quantitatively or qualitatively abnormal. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor VIII, and impaired platelet adhesion.
Terms: von Willebrand Diseases Preferred Term
Term UI T746762
Date02/27/2009
LexicalTag EPO
ThesaurusID NLM (2010); Hemophilia, Vascular
Term UI T043387
Date04/20/1989
LexicalTag NON
ThesaurusID NLM (1990); Vascular Pseudohemophilia
Term UI T842673
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Von Willebrand's Factor Deficiency
Term UI T842675
Date04/18/2013
LexicalTag EPO
ThesaurusID GHR (2014); Von Willebrand Disorder
Term UI T842674
Date04/18/2013
LexicalTag EPO
ThesaurusID GHR (2014); von Willebrand's Disease
Term UI T043388
Date03/16/1981
LexicalTag EPO
ThesaurusID UNK (19XX); von Willebrand's Diseases
Term UI T746761
Date02/27/2009
LexicalTag EPO
ThesaurusID NLM (2010); Angiohemophilia
Term UI T043386
Date03/30/1974
LexicalTag NON
ThesaurusID; von Willebrand Disease
Term UI T043389
Date01/01/1999
LexicalTag EPO
ThesaurusID

von Willebrand Diseases MeSH Descriptor Data 2023