Congenital afibrinogenemia
MONDO:0008737Familial 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
15 clinical trials for this condition and its sub-types, 4 tagged with Congenital afibrinogenemia itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Part of
Sub-types of Congenital afibrinogenemia
-
Familial hypofibrinogenemia 3 trials
-
Familial hypodysfibrinogenemia 0 trials