Human genes for von Willebrand's disease 3
Von Willebrand's disease 3 [DOID:0111054]
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.
Synonyms: von Willebrand's disease 3, DOID:0111054, von Willebrands disease 3, von Willebrand disease type 3, von Willebrand disease type III ...