FGG, fibrinogen gamma chain, 2266

N. diseases: 70; N. variants: 18
Disease: Protein C Deficiency ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0398625
Disease: Protein C Deficiency
Protein C Deficiency 		0.010 Biomarker disease BEFREE Direct sequencing analyses were performed on FGA, FGB, and FGG genes to confirm hypodysfibrinogenemia and on the protein C gene to confirm protein C deficiency. 30632992 2019