"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 |
|---|
| 1996 | 1 | 0 | 1 |
| 2010 | 1 | 0 | 1 |
| 2012 | 1 | 0 | 1 |
| 2014 | 2 | 0 | 2 |
| 2017 | 1 | 0 | 1 |
| 2021 | 0 | 1 | 1 |
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Below are the most recent publications written about "Color Vision Defects" by people in Profiles.
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Phenotypic and Genetic Spectrum of Autosomal Recessive Bestrophinopathy and Best Vitelliform Macular Dystrophy. Invest Ophthalmol Vis Sci. 2021 05 03; 62(6):22.
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Endoplasmic reticulum (ER) Ca2+-channel activity contributes to ER stress and cone death in cyclic nucleotide-gated channel deficiency. J Biol Chem. 2017 07 07; 292(27):11189-11205.
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Suppressing thyroid hormone signaling preserves cone photoreceptors in mouse models of retinal degeneration. Proc Natl Acad Sci U S A. 2014 Mar 04; 111(9):3602-7.
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Exploration of cone cyclic nucleotide-gated channel-interacting proteins using affinity purification and mass spectrometry. Adv Exp Med Biol. 2014; 801:57-65.
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Biochemical characterization of cone cyclic nucleotide-gated (CNG) channel using the infrared fluorescence detection system. Adv Exp Med Biol. 2012; 723:769-75.
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Long-term and age-dependent restoration of visual function in a mouse model of CNGB3-associated achromatopsia following gene therapy. Hum Mol Genet. 2011 Aug 15; 20(16):3161-75.
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Molecular pathogenesis of achromatopsia associated with mutations in the cone cyclic nucleotide-gated channel CNGA3 subunit. Adv Exp Med Biol. 2010; 664:245-53.
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Color vision measured with pseudoisochromatic plates at five-and-a-half years in eyes of children from the CRYO-ROP study. Invest Ophthalmol Vis Sci. 1996 Nov; 37(12):2467-74.