IgA nephropathy type 2 is a probably autosomal dominant disorder associated with genetic alterations at chromosome positions 4q26-q31 and 17q12-q22. The exact genes are not yet discovered.
IgA nephropathy | |||
CFHR1 | |||
CFHR3 | |||
CFHR5 | |||
IgA nephropathy type 1 | |||
IgA nephropathy type 2 | |||
IgA nephropathy type 3 | |||
1. |
Bisceglia L et al. (2006) Genetic heterogeneity in Italian families with IgA nephropathy: suggestive linkage for two novel IgA nephropathy loci. |
2. |
Paterson AD et al. (2007) Genome-wide linkage scan of a large family with IgA nephropathy localizes a novel susceptibility locus to chromosome 2q36. |
3. |
OMIM.ORG article Omim 613944 |