von Willebrand's disease

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von Wil·le·brand's disease

 (vŏn wĭl′ə-brăndz′, fôn vĭl′ə-bränts′)
A genetic disorder characterized by a tendency to hemorrhage, caused by a clotting factor that affects platelet adhesion.

[After Erik Adolf von Willebrand, (1870-1949), Finnish physician.]
American Heritage® Dictionary of the English Language, Fifth Edition. Copyright © 2016 by Houghton Mifflin Harcourt Publishing Company. Published by Houghton Mifflin Harcourt Publishing Company. All rights reserved.
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Noun1.Von Willebrand's disease - a form of hemophilia discovered by Erik von Willebrandvon Willebrand's disease - a form of hemophilia discovered by Erik von Willebrand; a genetic disorder that is inherited as an autosomal recessive trait; characterized by a deficiency of the coagulation factor and by mucosal bleeding
bleeder's disease, haemophilia, hemophilia - congenital tendency to uncontrolled bleeding; usually affects males and is transmitted from mother to son
Based on WordNet 3.0, Farlex clipart collection. © 2003-2012 Princeton University, Farlex Inc.

Von Willebrand's disease

n. Von Willebrand, enfermedad de, desorden hereditario de la sangre caracterizado por episodios hemorrágicos gen. en las membranas mucosas.
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References in periodicals archive ?
Brown et al., "Is it congenital or acquired von Willebrands disease?," Haemophilia, vol.
Collagen binding assay for von Willebrand factor (VWF:CBA): detection of von Willebrands disease (VWD), and discrimination of VWD subtypes, depends on collagen source.
The Greenhead College student suffers from a severe bleeding condition called Von Willebrands disease type 3, causing her to spontaneously bleed.