has characteristic has characteristic hemorrhagic disease hereditary von Willebrand disease https://www.malacards.org/card/von_willebrands_disease von Willebrand disorder vascular haemophilia MedDRA:10047715 congenital von willebrand's disease SCTID:234446004 hereditary von Willebrand disease MONDO:0019565 von Willebrand-Jurgens disease UMLS:C5703318 vascular hemophilia von Willebrand disease Orphanet:903 von Willebrand's-Jurgens' disease hereditary von Willebrand disease (hereditary or acquired) icd11.foundation:2112021600 Hereditary von Willebrand disease (VWD) is a hereditary bleeding disorder caused by a genetic anomaly leading to quantitative, structural or functional abnormalities of the Willebrand factor (von Willebrand factor; VWF). Two major groups of VWF deficiency have been defined: quantitative and partial (type 1) or total (type 3), and qualitative (type 2) with several subtypes (2A, 2B, 2M, 2N). DOID:12531 MEDGEN:1814986 MESH:C531844 inherited inherited blood coagulation disorder von Willebrand disease (hereditary or acquired)