Congenital prothrombin deficiency

Congenital factor II deficiency is an inherited bleeding disorder due to reduced activity of factor II (FII, prothrombin) and characterized by mucocutaneous bleeding symptoms.

Also known as: factor 2 deficiency, factor II deficiency, hypoprothrombinemia, prothrombin deficiency, Dysprothrombinemia, congenital prothrombin deficiency, hereditary prothrombin deficiency, congenital factor II deficiency

46 clinical trials for this condition and its sub-types.