CFHR5

complement factor H related 5
OMIM: 608593
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Unexplained young onset end-stage renal disease
R-numbers: R197
Signed-off version 3.4
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
C3 glomerulopathy, C3G, Immune complex MPGN, IC-MPGN, Nephropathy due to CFHR5 deficiency, OMIM:614809, Immune-complex-mediated MPGN, CFHR5 nephropathy, Haematuria, Chronic Kidney Disease, Proteinuria, End stage renal disease