Familial Dysfibrinogenemia, also known as dysfibrinogenemia, familial, is related to dysfibrinogenemia, congenital and afibrinogenemia, congenital. An important gene associated with Familial Dysfibrinogenemia is FGG (Fibrinogen Gamma Chain), and among its related pathways/superpathways are MyD88 dependent cascade initiated on endosome and Class I MHC mediated antigen processing and presentation. Affiliated tissues include liver and kidney, and related phenotypes are gastrointestinal hemorrhage and epistaxis