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poruchy farebného videnia

  1. Subject h.poruchy farebného videnia
    Subject h.Color Vision Defects
    Entry termsporuchy videnia farieb
    achromatopsia
    farboslepota
    monochromatopsia
    English X referencesAchromatopsia
    Color Blindness
    Monochromatopsia
    Scope note in EnglishDefects 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.
    See also reference (FX) in Slovak bunky čapíkov sietnice, fotoreceptorové
    choroby sietnice
    See also reference (FX) in English Retinal Cone Photoreceptor Cells
    Retinal Diseases
    Links (4) - ARTICLES
    (3) - MeSH descriptor
    (1) - CiBaMed
    (1) - ELECTRONIC RESOURCES
    (6) - BOOKS
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Number of the records: 1  

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