Congenital prothrombin deficiency

MONDO:0013361

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

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