Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders

IgA nephropathy type 3

IgA nephropathy type 3 is an autosomal dominant disorder caused by mutations of the SPRY2 gene.

Systematic

IgA nephropathy
CFHR1
CFHR3
CFHR5
IgA nephropathy type 1
IgA nephropathy type 2
IgA nephropathy type 3
SPRY2

References:

1.

Milillo A et al. (2015) A SPRY2 mutation leading to MAPK/ERK pathway inhibition is associated with an autosomal dominant form of IgA nephropathy.

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2.

OMIM.ORG article

Omim 616818 [^]
Update: April 29, 2019