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Gyrate Atrophy MeSH Descriptor Data 2022


MeSH Heading
Gyrate Atrophy
Tree Number(s)
C11.270.468
C11.941.160.578
C16.320.290.468
Unique ID
D015799
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D015799
Annotation
a hered eye dis; /‌congen permitted: read MeSH definition
Scope Note
Progressive, autosomal recessive, diffuse atrophy of the choroid, pigment epithelium, and sensory retina that begins in childhood.
Entry Term(s)
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 Keto Acid Aminotransferase Deficiency
Ornithine Ketoacid Aminotransferase Deficiency
Ornithine-Delta-Aminotransferase Deficiency
Ornithinemia with Gyrate Atrophy
Previous Indexing
Atrophy (1970-1989)
Choroid (1970-1989)
Retinal Degeneration (1970-1989)
Public MeSH Note
90
History Note
90
Date Established
1990/01/01
Date of Entry
1989/05/26
Revision Date
2013/07/08
Gyrate Atrophy Preferred
Ornithine Aminotransferase Deficiency Related
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