3B12 Von Willebrand disease

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2026-01

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.

inclusions

• Angiohaemophilia
• Factor VIII deficiency with vascular defect
• Vascular haemophilia
• Von Willebrand disease type 1
• Von Willebrand disease type 2
• Von Willebrand disease type 3

exclusions

• Acquired von Willebrand disease or syndrome  (3B2Y)
• factor VIII deficiency NOS  (3B10)
• factor VIII deficiency with functional defect  (3B10)

synonyms

• Von Willebrand disease
• Angiohaemophilia
• Factor VIII deficiency with vascular defect
• Minot-von Willebrand-Jurgen disease
• Vascular haemophilia
• Willebrand Jurgen thrombopathy
• angiohaemophilia A
• angiohaemophilia B
• pseudohaemophilia
• Von Willebrand disease type 1
• Von Willebrand disease type 2
• Von Willebrand disease type 2A
• Von Willebrand disease type 2B
• Von Willebrand disease type 2M
• Von Willebrand disease type 2N
• Von Willebrand disease type 3

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