Structured Summary
Abstract
Progressive, autosomal recessive, diffuse atrophy of the choroid, pigment epithelium, and sensory retina that begins in childhood.
MeSH Record
Classification
Broader headings
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MeSH Record
Synonyms
16 entry terms
- 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
- Atrophy, Gyrate
- OAT Deficiency
- OKT Deficiency
- Ornithine Aminotransferase Deficiency
- Ornithine Keto Acid Aminotransferase Deficiency
- Ornithine Ketoacid Aminotransferase Deficiency
- Ornithine-Delta-Aminotransferase Deficiency
- Deficiency, OAT
- Deficiency, OKT
- Deficiency, Ornithine Aminotransferase
- Deficiency, Ornithine-Delta-Aminotransferase
- Ornithine Delta Aminotransferase Deficiency
MeSH Record
Aspects Covered
35 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, congenital, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
Indexing Annotation
a hered eye dis; /congen permitted: read MeSH definition
MeSH Record
History Note
90
MeSH Record
Previous Indexing
- Atrophy (1970-1989)
- Choroid (1970-1989)
- Retinal Degeneration (1970-1989)
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. Gyrate Atrophy. Medical Subject Headings (MeSH). 2026. Unique ID D015799. http://id.nlm.nih.gov/mesh/2026/D015799
- Gyrate Atrophy. In: Wikipedia. https://en.wikipedia.org/wiki/Ornithine_aminotransferase_deficiency
- Gyrate Atrophy. In: Wikidata. https://www.wikidata.org/wiki/Q3629047