Congenital afibrinogenemia

Familial afibrinogenemia is a coagulation disorder characterized by bleeding symptoms due to a complete absence of circulating fibrinogen.

Also known as: factor I deficiency, afibrinogenemia, afibrinogenemia congenital, afibrinogenemia, congenital, familial afibrinogenemia, hypofibrinogenemia, congenital

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