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DeCS
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Descriptor English:
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Gyrate Atrophy
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Descriptor Spanish:
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atrofia girata
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Descriptor Portuguese:
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Atrofia Girata
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Synonyms English:
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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:
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C11.270.468
C11.941.160.578
C16.320.290.468
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Definition English:
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Progressive, autosomal recessive, diffuse atrophy of the choroid, pigment epithelium, and sensory retina that begins in childhood. |
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Indexing Annotation English:
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a hered eye dis; /congen permitted: read MeSH definition
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History Note English:
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90
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Allowable Qualifiers English:
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Record Number:
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24702
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Unique Identifier:
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D015799
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Occurrence in VHL:
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Similar:
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DeCS
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