"Color Vision Defects" 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.
Defects of color vision are mainly hereditary traits but can be secondary to acquired or developmental abnormalities in the CONES (RETINA). Severity of hereditary defects of color vision depends on the degree of mutation of the ROD OPSINS genes (on X CHROMOSOME and CHROMOSOME 3) that code the photopigments for red, green and blue.
| Descriptor ID |
D003117
|
| MeSH Number(s) |
C10.597.751.941.256 C11.966.256 C23.888.592.763.941.256
|
| Concept/Terms |
Color Vision Defects- Color Vision Defects
- Color Vision Defect
- Defect, Color Vision
- Defects, Color Vision
- Vision Defect, Color
- Vision Defects, Color
- Color Vision Deficiency
Color Blindness, Red-Green- Color Blindness, Red-Green
- Color Blindness, Red Green
- Red-Green Color Blindness
- Deutan Defect
- Defect, Deutan
|
Below are MeSH descriptors whose meaning is more general than "Color Vision Defects".
Below are MeSH descriptors whose meaning is more specific than "Color Vision Defects".
This graph shows the total number of publications written about "Color Vision Defects" by people in this website by year, and whether "Color Vision Defects" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 0 | 1 | 1 |
| 2007 | 1 | 1 | 2 |
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Below are the most recent publications written about "Color Vision Defects" by people in Profiles.
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High-resolution microarray analysis unravels complex Xq28 aberrations in patients and carriers affected by X-linked blue cone monochromacy. Clin Genet. 2016 Jan; 89(1):82-7.
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Mutation of ATF6 causes autosomal recessive achromatopsia. Hum Genet. 2015 Sep; 134(9):941-50.
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Achromatopsia: the CNGB3 p.T383fsX mutation results from a founder effect and is responsible for the visual phenotype in the original report of uniparental disomy 14. Hum Genet. 2007 May; 121(3-4):433-9.
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Decreased retinal nerve fibre layer thickness detected by optical coherence tomography in patients with ethambutol-induced optic neuropathy. Br J Ophthalmol. 2007 Jul; 91(7):895-7.
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A functional MRI case study of acquired cerebral dyschromatopsia. Neuropsychologia. 2000; 38(8):1170-9.
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Retinal degeneration characterizes a spinocerebellar ataxia mapping to chromosome 3p. Nat Genet. 1995 May; 10(1):89-93.