Primary hyperoxaluria
From SNPedia
At a minimum, these SNPs are known to be related, and others may also be
Primary hyperoxaluria of all types is characterized by kidney stones and kidney damage due to a buildup of calcium oxalate deposits. Defects in the glyoxylate reductase/hydroxypyruvate reductase GRHPR gene, inherited as an autosomal recessive condition, are the genetic cause of this disorder.