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Findis

Gyrate atrophy of choroid and retina (HOGA)

Genes

  • OAT - ornithine aminotransferase (OAT)

Summary

Links

UMLS Concepts by OMIM 258870

C0018425 / HOGA / GYRATE ATROPHY OF CHOROID AND RETINA / GACR / HYPERORNITHINEMIA WITH GYRATE ATROPHY OF CHOROID AND RETINA / GYRATE ATROPHY
Other concept sources:
  • MSH D015799 - Atrophy, Gyrate
  • MTH NOCODE - Gyrate Atrophy
  • NCI C84744 - Gyrate Atrophy
  • LNC LA21166-6 - Gyrate atrophy
  • SNOMEDCT_US 314467007 - Gyrate atrophy
C0599035 / ORNITHINE KETO ACID AMINOTRANSFERASE DEFICIENCY / ORNITHINE-DELTA-AMINOTRANSFERASE DEFICIENCY / ORNITHINE AMINOTRANSFERASE DEFICIENCY / OAT DEFICIENCY / OKT DEFICIENCY
Other concept sources:
  • MTH NOCODE - Hyperornithinemia
  • SNOMEDCT_US 276426004 - Ornithine oxo-acid aminotransferase deficiency
  • MSH D015799 - Deficiency, Ornithine Aminotransferase
  • HPO HP:0012026 - Hyperornithinemia

Selected publications