Dysfibrinogenemia, Congenital (DYSFIBRIN)

Dysfibrinogenemia, Congenital, also known as hypodysfibrinogenemia, is related to familial dysfibrinogenemia and afibrinogenemia, congenital. An important gene associated with Dysfibrinogenemia, Congenital is FGA (Fibrinogen Alpha 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 whole blood.