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Results 1 - 6 of 6 for Afibrinogenemia
  1. Congenital afibrinogenemia is a bleeding disorder caused by impairment of the blood clotting process. Normally, blood clots protect the body after an injury by ...
  2. ... person will have a complete lack of fibrinogen (afibrinogenemia). When the abnormal gene is passed down from ...
  3. Rare Clotting Factor Deficiencies (World Federation of Hemophilia)  
    Bleeding Disorders/Specifics ... Bleeding Disorders ... Vitamin K/Learn More ... Vitamin K ... World Federation of Hemophilia
  4. ... in the FGA gene can lead to congenital afibrinogenemia, a condition that causes excessive bleeding due to ... the excessive bleeding seen in people with congenital afibrinogenemia. More About This Health Condition Mutations in one ...
  5. ... in the FGG gene can lead to congenital afibrinogenemia, a condition that causes excessive bleeding due to ... the excessive bleeding seen in people with congenital afibrinogenemia. More About This Health Condition Mutations in one ...
  6. ... in the FGB gene can lead to congenital afibrinogenemia, a condition that causes excessive bleeding due to ... in the human beta fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretion. Blood. 2000 Feb 15; ...