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Familial dysfibrinogenemia

MONDO:0014452

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

16 clinical trials for this condition and its sub-types, 2 tagged with Familial dysfibrinogenemia itself.

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Sub-types of Familial dysfibrinogenemia

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