Corneal Dystrophies, Hereditary
"Corneal Dystrophies, Hereditary" 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.
Bilateral hereditary disorders of the cornea, usually autosomal dominant, which may be present at birth but more frequently develop during adolescence and progress slowly throughout life. Central macular dystrophy is transmitted as an autosomal recessive defect.
Descriptor ID |
D003317
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MeSH Number(s) |
C11.204.236 C11.270.162 C16.320.290.162
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Concept/Terms |
Corneal Dystrophies, Hereditary- Corneal Dystrophies, Hereditary
- Corneal Dystrophy, Hereditary
- Dystrophies, Hereditary Corneal
- Dystrophy, Hereditary Corneal
- Hereditary Corneal Dystrophies
- Hereditary Corneal Dystrophy
Stromal Dystrophies, Corneal- Stromal Dystrophies, Corneal
- Corneal Stromal Dystrophies
- Corneal Stromal Dystrophy
- Dystrophies, Corneal Stromal
- Dystrophy, Corneal Stromal
- Stromal Dystrophy, Corneal
Granular Dystrophy, Corneal- Granular Dystrophy, Corneal
- Corneal Granular Dystrophies
- Corneal Granular Dystrophy
- Dystrophies, Corneal Granular
- Dystrophy, Corneal Granular
- Granular Dystrophies, Corneal
Macular Dystrophy, Corneal- Macular Dystrophy, Corneal
- Corneal Macular Dystrophies
- Corneal Macular Dystrophy
- Dystrophies, Corneal Macular
- Dystrophy, Corneal Macular
- Macular Dystrophies, Corneal
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Below are MeSH descriptors whose meaning is more general than "Corneal Dystrophies, Hereditary".
Below are MeSH descriptors whose meaning is more specific than "Corneal Dystrophies, Hereditary".
This graph shows the total number of publications written about "Corneal Dystrophies, Hereditary" by people in UAMS Profiles by year, and whether "Corneal Dystrophies, Hereditary" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Corneal Dystrophies, Hereditary" by people in Profiles over the past ten years.
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Wang S, Singh RB, Yuksel E, Musayeva A, Sinha S, Taketani Y, Dohlman TH, Dana R. Ocular pain in ocular graft-versus-host disease patients with neurotrophic keratopathy. Ocul Surf. 2022 10; 26:142-147.
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Myers EJ, Marshall A, Jennings ML, Parker MD. Mouse Slc4a11 expressed in Xenopus oocytes is an ideally selective H+/OH- conductance pathway that is stimulated by rises in intracellular and extracellular pH. Am J Physiol Cell Physiol. 2016 Dec 01; 311(6):C945-C959.
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