|Name||von Willebrand's disease 3|
|Definition||A von Willebrand's disease characterized by autosomal recessive inheritance of a severe quantitative defect or virtual absence of VWF in plasma, prolonged bleeding time, and more severe bleeding tendencies compared to the other types of von Willebrand disease that has material_basis_in homozygous or compound heterozygous mutation in the VWF gene which maps to chromosome 12p13.
von Willebrand disease type 3 [EXACT]
von Willebrand disease type III [EXACT]
VWD type 3 [EXACT]