CFHR3, complement factor H related 3, 10878

N. diseases: 55; N. variants: 5
Disease: Familial Atypical Hemolytic Uremic Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4055018
Disease: Familial Atypical Hemolytic Uremic Syndrome
Familial Atypical Hemolytic Uremic Syndrome 		0.010 GeneticVariation disease BEFREE A novel hybrid CFH/CFHR3 gene generated by a microhomology-mediated deletion in familial atypical hemolytic uremic syndrome. 22058112 2012