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von Willebrand's disease

[fawn vil-uh-brahnts] /fɔn ˈvɪl əˌbrɑnts/
noun, Pathology
an inherited autosomal recessive disease in which abnormally slow coagulation of blood may lead to spontaneous bleeding, excessive bleeding following an injury, and heavy menstrual flow.
1940-45; after Erik Adolf von Willebrand (1870-1949), Finnish physician Unabridged
Based on the Random House Dictionary, © Random House, Inc. 2014.
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von Willebrand's disease in Medicine

von Willebrand's disease von Wil·le·brand's disease (vŏn wĭl'ə-brāndz', fôn vĭl'ə-bränts')
A hereditary predisposition to hemorrhaging characterized by bleeding from mucous membranes and various abnormalities in the blood components responsible for clotting. Also called angiohemophilia, vascular hemophilia.

The American Heritage® Stedman's Medical Dictionary
Copyright © 2002, 2001, 1995 by Houghton Mifflin Company. Published by Houghton Mifflin Company.
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