FGG, fibrinogen gamma chain, 2266

N. diseases: 70; N. variants: 18
Disease: Hemophilia B ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0008533
Disease: Hemophilia B
Hemophilia B 		0.010 GeneticVariation disease BEFREE Coexisting congenital dysfibrinogenemia with a novel mutation in fibrinogen γ chain (γ322 Phe→Ile, Fibrinogen Beijing) and haemophilia B in a family. 25982359 2015