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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