has characteristic has characteristic hemorrhagic disease hereditary von Willebrand disease https://github.com/monarch-initiative/mondo/issues/10494 https://www.malacards.org/card/von_willebrands_disease von Willebrand disorder vascular haemophilia MedDRA:10047715 congenital von willebrand's disease hereditary pseudohaemophilia SCTID:234446004 hereditary von Willebrand disease MONDO:0019565 von Willebrand-Jurgens disease UMLS:C5703318 vascular hemophilia A von Willebrand disease that is inherited and characterized by impaired primary hemostasis resulting from germline genetic variation affecting von Willebrand factor quantity, von Willebrand factor function, platelet interaction with von Willebrand factor, or related hemostatic mechanisms. It is clinically characterized by defective platelet adhesion and secondary coagulation defect that manifests as abnormal bleeding of variable severity occurring either spontaneously or in association with an invasive procedure. von Willebrand disease Orphanet:903 von Willebrand's-Jurgens' disease hereditary von Willebrand disease (hereditary or acquired) icd11.foundation:2112021600 DOID:12531 MEDGEN:1814986 MESH:C531844 inherited inherited blood coagulation disorder von Willebrand disease (hereditary or acquired)