IgA nephropathy type 3 is an autosomal dominant disorder caused by mutations of the SPRY2 gene.
IgA nephropathy | ||||
CFHR1 | ||||
CFHR3 | ||||
CFHR5 | ||||
IgA nephropathy type 1 | ||||
IgA nephropathy type 2 | ||||
IgA nephropathy type 3 | ||||
SPRY2 | ||||
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. |
2. |
OMIM.ORG article Omim 616818 |