Von Willebrand disease type 2 (Q84145): Difference between revisions

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Latest revision as of 09:30, 15 August 2026

Type 2 von Willebrand disease is a form of VWD characterised by a bleeding disorder associated with a qualitative deficiency and functional anomalies of the Willebrand factor (von Willebrand factor; VWF). The type 2 disease accounts for between 20 and 45% of cases of VWD. Age of onset of the bleeding anomalies varies, with earlier onset being associated with more severe VWF deficiency. Four type 2 VWD subtypes have been described (types 2A, 2B, 2M and 2N).

Language	Label	Description	Also known as
default for all languages	ID_1658351780
English	Von Willebrand disease type 2	Type 2 von Willebrand disease is a form of VWD characterised by a bleeding disorder associated with a qualitative deficiency and functional anomalies of the Willebrand factor (von Willebrand factor; VWF). The type 2 disease accounts for between 20 and 45% of cases of VWD. Age of onset of the bleeding anomalies varies, with earlier onset being associated with more severe VWF deficiency. Four type 2 VWD subtypes have been described (types 2A, 2B, 2M and 2N).