Disease

Congenital Hypofibrinogenemia

About the Disease
Afibrinogenemia, Congenital, also known as congenital afibrinogenemia, is related to meningitis and meningococcal infection. An important gene associated with Afibrinogenemia, Congenital is FGG (Fibrinogen Gamma Chain), and among its related pathways/superpathways are Innate Immune System and Disease. The drugs Protamines and Thrombin have been mentioned in the context of this disorder. Affiliated tissues include spleen, tongue and liver, and related phenotypes are joint swelling and epistaxis

Common Targets
FGA | FGB | FGG | Fibrinogen

疾病靶点研报
Congenital Hypofibrinogenemia

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