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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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 Atrophies, Gyrate Atrophy, Gyrate Gyrate Atrophies

Below are MeSH descriptors whose meaning is more general than "Gyrate Atrophy".

Diseases [C]
Eye Diseases [C11]
Eye Diseases, Hereditary [C11.270]
Gyrate Atrophy [C11.270.468]
Uveal Diseases [C11.941]
Choroid Diseases [C11.941.160]
Gyrate Atrophy [C11.941.160.578]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Eye Diseases, Hereditary [C16.320.290]
Gyrate Atrophy [C16.320.290.468]

Below are MeSH descriptors whose meaning is more specific than "Gyrate Atrophy".

publications

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