Term Name:	von Willebrand's disease 3
Synonyms:	von Willebrand disease type 3, von Willebrand disease type III, VWD type 3, VWD3
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.
Ontology:	Human Disease [DOID:0111054]   ( DOID:0111054 )