Human genes for von Willebrand's disease 2
Von Willebrand's disease 2 [DOID:0060574]
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.
Synonyms: von Willebrand's disease 2, DOID:0060574, von Willebrands disease 2, von Willebrand disease type 2, von Willebrand disease type II ...