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Disease Gyrate Atrophy

Name Gyrate Atrophy
Synonyms Atrophy, Gyrate | Deficiency, OAT | Deficiency, OKT | Deficiency, Ornithine Aminotransferase | Deficiency, Ornithine-Delta-Aminotransferase | GACR | GYRATE ATROPHY | Gyrate Atrophy of Choroid and Retina | Gyrate Atrophy of the Choroid and Retina | HOGA | Hyperornithinemia with Gyrate Atrophy of Choroid and Retina | OAT Deficiency | OKT Deficiency | Ornithine Aminotransferase Deficiency | Ornithine Delta Aminotransferase Deficiency | Ornithine-Delta-Aminotransferase Deficiency | Ornithine Ketoacid Aminotransferase Deficiency | Ornithine Keto Acid Aminotransferase Deficiency | Ornithinemia with Gyrate Atrophy
Definition Progressive, autosomal recessive, diffuse atrophy of the choroid, pigment epithelium, and sensory retina that begins in childhood.
Categories Eye disease | Genetic disease (inborn)
MeSH® ID D015799
OMIM® ID 258870
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Top ↑ Ancestors

1. DiseasesEye Diseases Has associated chemicals Has associated genes Has associated exposure references Eye Diseases, Hereditary Has associated chemicals Has associated genes Gyrate Atrophy Has associated chemicals Has associated genes
2. DiseasesEye Diseases Has associated chemicals Has associated genes Has associated exposure references Uveal Diseases Has associated chemicals Has associated genes Choroid Diseases Has associated chemicals Has associated genes Gyrate Atrophy Has associated chemicals Has associated genes
3. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated exposure references Genetic Diseases, Inborn Has associated chemicals Has associated genes Has associated exposure references Eye Diseases, Hereditary Has associated chemicals Has associated genes Gyrate Atrophy Has associated chemicals Has associated genes

Top ↑ Descendants

Gyrate Atrophy Has associated chemicals Has associated genes
  Moloney syndrome