CFH, complement factor H, 3075

N. diseases: 393; N. variants: 150
Disease: Complement deficiency disease ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0272242
Disease: Complement deficiency disease
Complement deficiency disease 		0.300 Biomarker group GENOMICS_ENGLAND Characterization of a factor H mutation that perturbs the alternative pathway of complement in a family with membranoproliferative GN. 24722444 2014