| Descriptor English: | Gyrate Atrophy | ||||
| Descriptor Spanish: |
Atrofia Girata
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| Descriptor Portuguese: | Atrofia Girata | ||||
| Descriptor French: | Atrophie gyrée | ||||
| Entry term(s): |
Atrophy, Gyrate Deficiency, OAT Deficiency, OKT Deficiency, Ornithine Aminotransferase Deficiency, Ornithine-Delta-Aminotransferase 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 Delta Aminotransferase Deficiency Ornithine Keto Acid Aminotransferase Deficiency Ornithine Ketoacid Aminotransferase Deficiency Ornithine-Delta-Aminotransferase Deficiency Ornithinemia with Gyrate Atrophy |
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| Tree number(s): |
C11.270.468 C11.941.160.578 C16.320.290.468 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D015799 | ||||
| Scope note: | Progressive, autosomal recessive, diffuse atrophy of the choroid, pigment epithelium, and sensory retina that begins in childhood. |
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| Annotation: | a hered eye dis; /congen permitted: read MeSH definition |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Previous Indexing: |
Atrophy (1970-1989) Choroid (1970-1989) Retinal Degeneration (1970-1989) |
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| Public MeSH Note: | 90 |
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| History Note: | 90 |
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| DeCS ID: | 24702 | ||||
| Unique ID: | D015799 | ||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||
| Date Established: | 1990/01/01 | ||||
| Date of Entry: | 1989/05/26 | ||||
| Revision Date: | 2013/07/08 |
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DISEASES
Eye Diseases [C11]Eye Diseases -
DISEASES
Eye Diseases [C11]Eye Diseases
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Gyrate Atrophy
- Preferred
Ornithine Aminotransferase Deficiency
- Related but not broader or narrower
| Concept UI |
M0024200 |
| Scope note | Progressive, autosomal recessive, diffuse atrophy of the choroid, pigment epithelium, and sensory retina that begins in childhood. |
| Preferred term | Gyrate Atrophy |
| Entry term(s) |
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 |
| Concept UI |
M0531593 |
| Preferred term | Ornithine Aminotransferase Deficiency |
| Entry term(s) |
Deficiency, OAT Deficiency, OKT Deficiency, Ornithine Aminotransferase Deficiency, Ornithine-Delta-Aminotransferase OAT Deficiency OKT Deficiency Ornithine Delta Aminotransferase Deficiency Ornithine Keto Acid Aminotransferase Deficiency Ornithine Ketoacid Aminotransferase Deficiency Ornithine-Delta-Aminotransferase Deficiency |
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