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Results 1 - 7 of 7 for Congenital fibrinogen deficiency
  1. 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
  2. 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
  3. 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
  4. F7 gene 
    ... J. Clinical manifestations, management, and molecular genetics in congenital factor VII deficiency: the International Registry on Congenital Factor VII Deficiency (IRF7). Blood. 2000 Jul 1; ...
    https://medlineplus.gov/genetics/gene/f7 - Genetics
  5. F10 gene 
    ... Girolami A, Scarparo P, Scandellari R, Allemand E. Congenital factor X deficiencies with a defect only or ... Lombardi AM. Persistent validity of a classification of congenital factor X defects based on clotting, chromogenic and ...
    https://medlineplus.gov/genetics/gene/f10 - Genetics
  6. ITGA2B gene 
    ... the alphaIIbbeta3 receptor affects proplatelet formation and causes congenital macrothrombocytopenia. Blood. 2011 May 19;117(20):5479- ...
    https://medlineplus.gov/genetics/gene/itga2b - Genetics
  7. F11 gene 
    ... F11 NCBI Gene ClinVar Duga S, Salomon O. Congenital factor XI deficiency: an update. Semin Thromb Hemost. ...
    https://medlineplus.gov/genetics/gene/f11 - Genetics