Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
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
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CFHR1
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CFHR3
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CFHR5
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IgA nephropathy type 1
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IgA nephropathy type 2
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IgA nephropathy type 3
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| 1. |
Bisceglia L et al. (2006) Genetic heterogeneity in Italian families with IgA nephropathy: suggestive linkage for two novel IgA nephropathy loci. 
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| 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.
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| 3. |
OMIM.ORG article Omim 613944
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