Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja A rare, inherited bleeding disorder 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. Three main subtypes are defined based on the type of von Willebrand factor defect: partial (type 1) or total (type 3) deficiency, and qualitative/functional anomalies (type 2). Disease data Klasyfikacja Disease Synonimy Hereditary von Willebrand disease Choroba Willebrand Dziedziczna choroba Willebranda Kod ORPHA 903 Kod OMIM 613554 Kod ICD10 D68.0 Kod ICD11 3B12 *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl