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

Gå till den engelska sidan

Familial hypofibrinogenemia

MONDO:0015096

Familial hypofibrinogenemia is a coagulation disorder characterized by mild bleeding symptoms following trauma or surgery due to a reduced plasma fibrinogen concentration.

Also known as: hypofibrinogenemia, familial

13 clinical trials for this condition and its sub-types, 3 tagged with Familial hypofibrinogenemia itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by