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Gyrate Atrophy

Progressive, autosomal recessive, diffuse atrophy of the choroid, pigment epithelium, and sensory retina that begins in childhood.

Year introduced: 1990

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Subheadings:

Tree Number(s): C11.270.468, C11.941.160.578, C16.320.290.468

MeSH Unique ID: D015799

Entry Terms:

  • Atrophy, Gyrate
  • Gyrate Atrophy of Choroid and Retina
  • Gyrate Atrophy of the Choroid and Retina
  • Hyperornithinemia with Gyrate Atrophy of Choroid and Retina
  • Ornithinemia with Gyrate Atrophy
  • Ornithine Aminotransferase Deficiency
  • Deficiency, Ornithine Aminotransferase
  • OAT Deficiency
  • Deficiency, OAT
  • OKT Deficiency
  • Deficiency, OKT
  • Ornithine Keto Acid Aminotransferase Deficiency
  • Ornithine Ketoacid Aminotransferase Deficiency
  • Ornithine-Delta-Aminotransferase Deficiency
  • Deficiency, Ornithine-Delta-Aminotransferase
  • Ornithine Delta Aminotransferase Deficiency

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