Gyrate Atrophy
"Gyrate Atrophy" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Progressive, autosomal recessive, diffuse atrophy of the choroid, pigment epithelium, and sensory retina that begins in childhood.
| Descriptor ID |
D015799
|
| MeSH Number(s) |
C11.270.468 C11.941.160.578 C16.320.290.468
|
| Concept/Terms |
Gyrate Atrophy- Gyrate Atrophy
- Atrophy, Gyrate
- Ornithinemia with Gyrate Atrophy
- Hyperornithinemia with Gyrate Atrophy of Choroid and Retina
- Gyrate Atrophy of Choroid and Retina
- Gyrate Atrophy of the Choroid and Retina
Ornithine Aminotransferase Deficiency- Ornithine Aminotransferase Deficiency
- Deficiency, Ornithine Aminotransferase
- Ornithine-Delta-Aminotransferase Deficiency
- Deficiency, Ornithine-Delta-Aminotransferase
- Ornithine Delta Aminotransferase Deficiency
- Ornithine Keto Acid Aminotransferase Deficiency
- Ornithine Ketoacid Aminotransferase Deficiency
- OAT Deficiency
- Deficiency, OAT
- OKT Deficiency
- Deficiency, OKT
|
Below are MeSH descriptors whose meaning is more general than "Gyrate Atrophy".
Below are MeSH descriptors whose meaning is more specific than "Gyrate Atrophy".
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