Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
Moldiag Diseases Genes Support Contact

Hyperoxaluria type 2

The autosomal recessive oxalosis 2 is hyperoxaluria, oxalate nephrolithiasis and nephrocalcinosis due to mutations of the GRHPR gene.

Systematic

Hyperoxaluria
Hyperoxaluria type 1
Hyperoxaluria type 2
GRHPR
Hyperoxaluria type 3
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