Primary hyperoxaluria type 1

Synonym(s)
- Alanine-glyoxylate aminotransferase deficiency
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- AGXT / Alanine-Glyoxylate Aminotransferase
  2q37.3
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Alanine-glyoxylate aminotransferase
Disease group(s)
- 13.3 Disorders of glyoxylate and oxalate metabolism