C68677Level 7
von Willebrand Disease
**Semantic type:** Disease or Syndrome
**Definition:** Hereditary or acquired coagulation disorder characterized by a qualitative or quantitative deficiency of the von Willebrand factor. The latter plays an important role in platelet adhesion. Signs and symptoms include bruises, nose bleeding, gum bleeding following a dental procedure, heavy menstrual bleeding, and gastrointestinal bleeding.
**Synonyms:** - Von Willebrand's disease - von Willebrand Disorder - von Willebrand's Disease
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