" /> Von Willebrand disease - CISMeF





ICD-11 code : 3B12;

Preferred Label : Von Willebrand disease;

ICD-11 definition : 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.;

ICD-11 synonym : Factor VIII deficiency with vascular defect; Vascular haemophilia; pseudohaemophilia; angiohemophilia B; Willebrand Jurgen thrombopathy; angiohemophilia A;

ICD-11 inclusion : Minot-von Willebrand-Jurgen disease; Angiohaemophilia; Vascular haemophilia; Factor VIII deficiency with vascular defect;

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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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11/05/2025


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