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von Willebrand Diseases

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.

Year introduced: 2010(1963)

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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

MeSH Unique ID: D014842

Entry Terms:

  • Hemophilia, Vascular
  • Vascular Hemophilia
  • Vascular Hemophilias
  • Vascular Pseudohemophilia
  • Pseudohemophilia, Vascular
  • Pseudohemophilias, Vascular
  • Vascular Pseudohemophilias
  • Von Willebrand's Factor Deficiency
  • Von Willebrand Disorder
  • Disorder, Von Willebrand
  • von Willebrand's Disease
  • von Willebrand's Diseases
  • Angiohemophilia
  • Angiohemophilias
  • von Willebrand Disease
  • von Willebrand Disease, Recessive Form

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