Familial dysfibrinogenemia

Familial dysfibrinogenemia is a coagulation disorder characterized by a bleeding tendency due to a functional anomaly of circulating fibrinogen.

Also known as: dysfibrinogenemia, familial dysfibrinogenemia, hypodysfibrinogenemia, congenital dysfibrinogenemia, dysfibrinogenemia, congenital, dysfibrinogenemia, familial, hypodysfibrinogenemia, congenital

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