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Results 1 - 9 of 9 for Congenital fibrinogen deficiency
  1. Congenital afibrinogenemia 
    ... P, Neerman-Arbez M. FGB mutations leading to congenital quantitative fibrinogen deficiencies: an update and report of four novel mutations. ...
    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. Factor XIII deficiency 
    ... Testing Registry: Factor XIII, A subunit, deficiency of Congenital factor XIII deficiency National Organization for Rare Disorders ( ... R, Ariens RA, Muszbek L; Factor XIII And Fibrinogen SSC Subcommittee Of The ISTH. ... of factor XIII deficiencies. J Thromb Haemost. 2011 Jul;9(7):1404- ...
    https://medlineplus.gov/genetics/condition/factor-xiii-deficiency - Genetics
  6. 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
  7. 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
  8. 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
  9. 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