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poruchy farebného videnia

  1. Record numberd003117
    Date06.06.2025
    TypeM - MESH
    Topical termporuchy farebného videnia
    Other termEnglish (Pseudonym) Achromatopsia
    English (Pseudonym) Color Blindness
    English (Pseudonym) Monochromatopsia
    Slovak (Pseudonym) poruchy videnia farieb
    Slovak (Pseudonym) achromatopsia
    Slovak (Pseudonym) farboslepota
    Slovak (Pseudonym) monochromatopsia
    See also(Skutočné meno) choroby sietnice
    (Skutočné meno) bunky čapíkov sietnice, fotoreceptorové
    (Later heading) vnímanie farieb
    UDCC10.597.751.941.256C11.270.151.500C11.966.256C23.888.592.763.941.256
    NoteDefects 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.
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Number of the records: 1  

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