Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition A rare inherited bleeding disorder due to reduced activity of factor II (FII, prothrombin) and characterized by mucocutaneous and soft tissue bleeding symptoms. Disease data Classification Disease Synonyms Dysprothrombinemia Dysprotrombinemia Hipoprothrombinemia Niedobór protrombiny Hypoprothrombinemia Prothrombin deficiency ORPHA code 325 OMIM code 613679 ICD10 code D68.2 ICD11 code 3B14.Z *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