CFH, complement factor H, 3075

N. diseases: 393; N. variants: 150
Disease: Complement abnormality ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0272241
Disease: Complement abnormality
Complement abnormality 		0.010 Biomarker disease BEFREE The most common mutation is in the gene encoding complement factor H. Combined liver-kidney transplantation may correct this complement abnormality and prevent recurrence when the defect involves genes encoding circulating proteins that are synthesized in the liver, such as factor H or I. 19092117 2009