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Color Blindness Simulator

See how your palette looks to people with different types of color vision deficiency. Enter up to 6 colors, then check each simulation row below.

Your palette

5 / 6 colors
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Normal vision~92% of people

Full trichromatic color vision — three functioning cone types.

Protanopia~1% of men

Red-blind. L-cones (red) are absent. Reds appear dark; confusion between red, green, and brown.

#9B9A43
#5C5D95
#5C5D92
#D9D980
#343450
Deuteranopia~1% of men

Green-blind. M-cones (green) are absent. Most common form. Greens and reds are easily confused.

#A5B242
#595593
#554D93
#DBDE85
#32304F
Tritanopia<0.01% of people

Blue-blind. S-cones (blue) are absent. Blues appear green; yellows appear violet or grey.

#DD4040
#488E8D
#309596
#E79195
#284D4D
Achromatopsia~0.003% of people

Complete color blindness. No functional cones — only rod-based monochromatic vision.

#6E6E6E
#6F6F6F
#797979
#C5C5C5
#3E3E3E

About color vision deficiency

How common is it?

Color vision deficiency affects roughly 8% of men and 0.5% of women of Northern European descent. Deuteranomaly (reduced green sensitivity) is by far the most common form, followed by protanomaly (reduced red sensitivity). Tritanopia and complete achromatopsia are rare.

What makes a palette accessible?

A palette accessible to color-blind users relies on more than hue — lightness contrast is the most robust signal. Use the Contrast Checker to verify text legibility, and avoid communicating information through color alone (use icons, labels, or patterns too).

Red–green confusion

Protanopia and deuteranopia both cause confusion between reds, greens, and browns. If your palette contains red and green together as the only distinguishing cues (e.g. status indicators), consider adding blue or ensuring strong lightness difference between them.

Simulator limitations

This simulator uses the Viénot et al. transformation matrices, which model dichromacy (complete absence of a cone type). Real-world color vision deficiency is a spectrum — many people have reduced sensitivity rather than full absence. Use this as a design sanity check, not a clinical tool.