Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja A rare genetic coagulation disorder characterized by marked bleeding tendency and posttraumatic bleeding with easy bruising, soft tissue and muscle bleeding, hemarthroses, and menorrhagia due to an increase of soluble thrombomodulin in plasma with subsequent protein C activation and reduction of thrombin generation within a potential thrombus. Abnormal laboratory findings include markedly elevated plasma thrombomodulin, reduced prothrombin consumption, and decreased thrombin generation. Disease data Klasyfikacja Disease Synonimy THBD-related bleeding disorder Koagulopatia zależna od THBD Koagulopatia zależna od trombomoduliny Zaburzenia krzepnięcia zależne od THBD THBD-related coagulopathy Thrombomodulin-related coagulopathy Kod ORPHA 436169 Kod OMIM 614486 Kod ICD10 D68.3 Kod ICD11 - *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