Gyrate Atrophy

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

Also Known As:

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

Eye Diseases: 3522
- Hereditary Eye Diseases: 18
  - Gyrate Atrophy: 246
- Uveal Diseases: 16
  - Choroid Diseases: 94
    - Gyrate Atrophy: 246
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Hereditary Eye Diseases: 18
    - Gyrate Atrophy: 246

White J Fiona Selected Research

White J Fiona Research Topics

Disease

Drug/Important Bio-Agent (IBA)