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Results 1 - 6 of 6 for "Afibrinogenemia," congenital
  1. Congenital afibrinogenemia 
    ... National Organization for Rare Disorders (NORD) ClinicalTrials.gov AFIBRINOGENEMIA, CONGENITAL PubMed Casini A, Lukowski S, Quintard VL, Crutu ...
    https://medlineplus.gov/.../condition/congenital-afibrinogenemia - Genetics
  2. FGA gene 
    ... Mutations in the FGA gene can lead to congenital afibrinogenemia, a condition that causes excessive bleeding due to ... to the excessive bleeding seen in people with congenital afibrinogenemia. More About This Health Condition Mutations in one ...
    https://medlineplus.gov/genetics/gene/fga - Genetics
  3. FGB gene 
    ... Mutations in the FGB gene can lead to congenital afibrinogenemia, a condition that causes excessive bleeding due to ... mutations in the human beta fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretion. Blood. 2000 Feb 15; ...
    https://medlineplus.gov/genetics/gene/fgb - Genetics
  4. FGG gene 
    ... Mutations in the FGG gene can lead to congenital afibrinogenemia, a condition that causes excessive bleeding due to ... to the excessive bleeding seen in people with congenital afibrinogenemia. More About This Health Condition Mutations in one ...
    https://medlineplus.gov/genetics/gene/fgg - Genetics
  5. Rare Clotting Factor Deficiencies (World Federation of Hemophilia)  
    Bleeding Disorders/Specifics ... Bleeding Disorders ... Vitamin K/Learn More ... Vitamin K ... World Federation of Hemophilia
    https://elearning.wfh.org/.../rare-clotting-factor-deficiencies - External Health Links
  6. Congenital fibrinogen deficiency 
    Congenital fibrinogen deficiency is a very rare, inherited blood disorder in which the blood does not clot normally. It affects a protein called fibrinogen. This protein is needed for the blood to clot.
    https://medlineplus.gov/ency/article/001313.htm - Medical Encyclopedia