CFH, complement factor H, 3075

N. diseases: 393; N. variants: 150
Disease: Afibrinogenemia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0001733
Disease: Afibrinogenemia
Afibrinogenemia 		0.010 GeneticVariation disease BEFREE Inherited complete factor I deficiency associated with systemic lupus erythematosus, higher susceptibility to infection and low levels of factor H. 11422911 2001