CFH, complement factor H, 3075

N. diseases: 393; N. variants: 150
Disease: Familial hemolytic uremic syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4302342
Disease: Familial hemolytic uremic syndrome
Familial hemolytic uremic syndrome 		0.010 GeneticVariation disease BEFREE The molecular basis of familial hemolytic uremic syndrome: mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20. 11158219 2001