Ornithine aminotransferase deficiency

(OAT deficiency)

Synonym(s)
- Gyrate atrophy of choroid and retina
Type

Disease
External link(s)
Gene
- OAT / ornithine aminotransferase
  10q26.13
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Ornithine aminotransferase
Pathway
- Ornithine, proline and hydroxyproline metabolism
Disease group(s)
- 1.7 Disorders of ornithine, proline and hydroxyproline metabolism