Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

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

12 clinical trials for this condition and its sub-types, 0 tagged with Congenital prothrombin deficiency itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by