Panel | Mode of inheritance | Details |
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1 panel | ||
Component of the following Super Panels:
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 |