DO_rare_slim NCIthesaurus has symptom von Willebrand's disease 3 disease_ontology ICD10CM:D68.03 MESH:D056729 SNOMEDCT_US_2025_09_01:128108002 ORDO:166096 NCI:C85213 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. DOID:0111054 MIM:277480 UMLS_CUI:C1264041 VWD type 3 VWD3 von Willebrand disease type 3 von Willebrand disease type III von Willebrand's disease bleeding