OnlineIMD

Primary hyperoxaluria type 3

  • Synonym(s)
    • 4-Hydroxy-2-oxoglutarate aldolase 1 deficiency
  • Type
    Disease
  • External link(s)
    • Orphanet
    • IEMbase
  • Gene
    • HOGA1 / hydroxyglutarate dehydrogenase 1
      • 10q24.2
      • OMIM
      • GnomAD
      • Ensembl
      • HGNC
      • VMH
      • LOVD
  • Gene product
    • Hydroxyglutarate dehydrogenase
  • Pathway
    • Ornithine, proline and hydroxyproline metabolism
  • Disease group(s)
    • 1.7        Disorders of ornithine, proline and hydroxyproline metabolism