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. Author manuscript; available in PMC: 2020 Nov 2.
Published in final edited form as: Eur J Haematol. 2019 May 31;103(2):73–79. doi: 10.1111/ejh.13250

Table 1.

Classification of von Willebrand disease.

Quantitative deficiency of VWF
Type 1 Partial quantitative deficiency of VWF
Type 3 Virtually complete deficiency of VWF
Qualitative deficiency of VWF
Type 2 Qualitative deficiency of VWF
- Type 2A Qualitative variants with decreased platelet-dependent function associated with the absence of high and intermediate-molecular-weight VWF multimers
- Type 2B Qualitative variants with increased affinity for platelet GPIb
- Type 2M Qualitative variants with decreased platelet-dependent function not caused by the absence of high-molecular-weight VWF multimers
- Type 2N Qualitative variants with markedly decreased affinity for factor VIII