Your browser does not support javascript:   Search for gard hereSearch for news-and-events here.


Genetic and Rare Diseases Information Center (GARD)

Print friendly version

Primary hyperoxaluria type 1

See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.

Other Names for Primary hyperoxaluria type 1

  • Alanine-glyoxylate aminotransferase deficiency
  • Glycolic aciduria
  • Hepatic AGT deficiency
  • HP1
  • Oxalosis 1
  • Peroxisomal alanine glyoxylate aminotransferase deficiency
  • Serine pyruvate aminotransferase deficiency