"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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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1996 | 1 | 0 | 1 |
| 1998 | 1 | 0 | 1 |
| 2006 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Color Vision Defects" by people in Profiles.
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Magacho L, Henderer JD, Lankaranian D, Steinmann WC, Spaeth GL. Improvement in colour vision parameters following successful trabeculectomy. Acta Ophthalmol Scand. 2006 Apr; 84(2):201-5.
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Eagle RC. Laser pointers and color blindness. Ophthalmology. 1998 May; 105(5):760.
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Ruberg FL, Skene DJ, Hanifin JP, Rollag MD, English J, Arendt J, Brainard GC. Melatonin regulation in humans with color vision deficiencies. J Clin Endocrinol Metab. 1996 Aug; 81(8):2980-5.
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Manon-Espaillat R, Gothe B, Adams N, Newman C, Ruff R. Familial 'sleep apnea plus' syndrome: report of a family. Neurology. 1988 Feb; 38(2):190-3.
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Johnston AW, Frost P, Spaeth GL, Renwick JH. Linkage relationships of the angiokeratoma (Fabry) locus. Ann Hum Genet. 1969 May; 32(4):369-74.