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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Where it sits in the disease tree

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Part of

↑ Congenital fibrinogen deficiency (6)

Sub-types of Familial dysfibrinogenemia

Congenital afibrinogenemia 4 trials · 5 incl. sub-types
2 sub-types
- Familial hypofibrinogenemia 3 trials
- Familial hypodysfibrinogenemia 0 trials

Including sub-types (16) Tagged with Familial dysfibrinogenemia (2)

Not yet recruiting 1 Completed 1

New blood treatment could save trauma patients faster

Disease control Not yet recruiting

This study tests whether a new shelf-stable blood product (IFC) works faster than the standard cryoprecipitate to stop severe bleeding in trauma patients. About 320 adults with traumatic injuries and low fibrinogen levels will be enrolled. The goal is to see if IFC can be given m…

Sponsor: Cerus Corporation • Aim: Disease control

Last updated Jun 27, 2026 14:00 UTC

Familial dysfibrinogenemia

Where it sits in the disease tree

New blood treatment could save trauma patients faster