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An Entity of Type : skos:Concept, within Data Space : data.idref.fr associated with source document(s)

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type
seeAlso
sameAs
notation
  • C10.597.751.941.256
  • C11.966.256
  • C23.888.592.763.941.256
  • C11.270.151.500
alternative label
  • Cécité des couleurs
  • Daltonisme
  • Color Blindness, Red Green
  • Color Blindness, Red-Green
  • Protan Defect
  • Achromatopsia
  • Color Blindness
  • Defects, Color Vision
  • Défauts de vision des couleurs
  • Déficiences de la vision des couleurs
  • Monochromatopsie du rouge
  • Vision Defect, Color
  • Vision Defects, Color
  • Achromatopsie
  • Acquired Color Blindness
  • Blindness, Color
  • Color Blindness, Acquired
  • Color Blindness, Green
  • Cécité acquise de la vision des couleurs
  • Cécité héréditaire de la vision des couleurs
  • Daltonisme rouge-vert
  • Monochromatopsie
  • Red Color Blindness
  • Blue Color Blindness
  • Color Blindness, Blue
  • Color Blindness, Inherited
  • Color Vision Defect
  • Color Vision Defects
  • Cécité au rouge-vert
  • Defect, Color Vision
  • Defect, Deutan
  • Dyschromatopsie acquise
  • Monochromatopsia
  • Protanomalie
  • Cécité au bleu
  • Cécité au rouge
  • Deutan Defect
  • Dyschromatopsies
  • Green Color Blindness
  • Monochromatopsie du bleu
  • Monochromatopsie du vert
  • Red-Green Color Blindness
  • Tritanomalie
  • Color Blindness, Red
  • Color Vision Deficiency
  • Cécité au vert
  • Deutéranomalie
  • Dyschromatopsie héréditaire
  • Déficiences de la vision colorée
  • Incapacité acquise de la perception des couleurs
  • Inherited Color Blindness
  • Tritan Defect
  • Achromatopsias
  • Color Vision Deficiencies
  • Deficiencies, Color Vision
  • Deficiency, Color Vision
  • Vision Deficiencies, Color
  • Vision Deficiency, Color
preferred label
  • Troubles de la vision des couleurs
is in scheme
note
  • Severely deficient color perception, typically with monochromacy and reduced visual acuity. The atypical form can include normal visual acuity with pseudomonochromacy
  • 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
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