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