3B12 Von Willebrand disease

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01


A disease caused by inherited genetic mutations. This disease is characterised by quantitative, structural or function abnormalities of von Willebrand factor leading to abnormalities in coagulation of the blood. This disease may present with prolonged bleeding, easy bruising or bleeding gums. Confirmation is by identification of mutation through genetic testing.

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