Conditions / Other
von Willebrand's disease 2
info · Other · ICD-10: D68.02
A von Willebrand's disease characterized by qualitative but not quantitative abnormalities of the VWF protein that has_material_basis_in mutation in the VWF gene which maps to chromosome 12p13.
Signs and symptoms
- Menorrhagia
- Bruising susceptibility
- Epistaxis
- Thrombocytopenia
Also known as: VWD type 2; VWD2; von Willebrand disease type 2; von Willebrand disease type II