Congenital afibrinogenemia

MONDO:0008737

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

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