Congenital factor II deficiency

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Name:
Congenital factor II deficiency
Description:
A rare inherited bleeding disorder due to reduced activity of factor II (FII, prothrombin) and characterized by mucocutaneous and soft tissue bleeding symptoms.
ORPHAcode:
325
Synonyms:
Dysprothrombinemia
Hypoprothrombinemia
Prothrombin deficiency
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