Von Willebrand disease (hereditary or acquired)

ICD-10 Code D68.0

Von Willebrand disease (hereditary or acquired)

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.

Also known as Von Willebrand Disease, von Willebrand disorder, von Willebrand's disease, VWD — per MONDO

Also identified as

Drugs indicated

Drug Relation Source
Desmopressin may treat MEDRT · Public domain (U.S. Government work)