"Eye Diseases, 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.
Transmission of gene defects or chromosomal aberrations/abnormalities which are expressed in extreme variation in the structure or function of the eye. These may be evident at birth, but may be manifested later with progression of the disorder.
| Descriptor ID |
D015785
|
| MeSH Number(s) |
C11.270 C16.320.290
|
| Concept/Terms |
Eye Diseases, Hereditary- Eye Diseases, Hereditary
- Disease, Hereditary Eye
- Diseases, Hereditary Eye
- Eye Disease, Hereditary
- Hereditary Eye Disease
- Hereditary Eye Diseases
|
Below are MeSH descriptors whose meaning is more general than "Eye Diseases, Hereditary".
Below are MeSH descriptors whose meaning is more specific than "Eye Diseases, Hereditary".
This graph shows the total number of publications written about "Eye Diseases, Hereditary" by people in this website by year, and whether "Eye Diseases, Hereditary" was a major or minor topic of these publications.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2016 | 0 | 1 | 1 |
| 2017 | 0 | 1 | 1 |
| 2018 | 5 | 0 | 5 |
| 2019 | 1 | 0 | 1 |
| 2020 | 0 | 1 | 1 |
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Below are the most recent publications written about "Eye Diseases, Hereditary" by people in Profiles.
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COVID-19: The Influence of ACE Genotype and ACE-I and ARBs on the Course of SARS-CoV-2 Infection in Elderly Patients. Clin Interv Aging. 2020; 15:1231-1240.
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Genetic Mutation Profiles in Korean Patients with Inherited Retinal Diseases. J Korean Med Sci. 2019 Jun 02; 34(21):e161.
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Revolution in evolution. Indian J Ophthalmol. 2018 12; 66(12):1667.
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Clinical Course of Autosomal Recessive Bestrophinopathy Complicated by Choroidal Neovascularization. Ophthalmic Surg Lasers Imaging Retina. 2018 11 01; 49(11):888-892.
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Swept source optical coherence tomography and optical coherence tomography angiography in pediatric enhanced S-cone syndrome: a case report. J Med Case Rep. 2018 Oct 03; 12(1):287.
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Familial Exudative Vitreoretinopathy Imaged With Optical Coherence Tomography Angiography. Ophthalmic Surg Lasers Imaging Retina. 2018 09 01; 49(9):e112-e113.
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Optical Coherence Tomography Angiography of Pigmented Paravenous Retinochoroidal Atrophy. Ophthalmic Surg Lasers Imaging Retina. 2018 05 01; 49(5):381-383.
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Osteoporosis-pseudoglioma syndrome: Report of two cases and a manifesting carrier. Ophthalmic Genet. 2017 Sep-Oct; 38(5):473-479.
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Large Deletions of TSPAN12 Cause Familial Exudative Vitreoretinopathy (FEVR). Invest Ophthalmol Vis Sci. 2016 12 01; 57(15):6902-6908.