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Colour Blindness: Types, Causes and How Testing Works

Protan, deutan and tritan deficiencies explained, how common each is, why it affects men more often, and what online screening can and cannot tell you.

Colour blindness is a misleading name. Most people with a colour vision deficiency can see colour; they see some colours as more alike than other people do. The most common form, difficulty telling reds from greens, affects about one man in twelve of Northern European descent. This article explains the types, why it is so much more common in men, how testing works, and what an online test can and cannot do.

How normal colour vision works

The retina holds three types of cone cell, each most sensitive to a range of wavelengths: long (L, roughly red), medium (M, roughly green) and short (S, roughly blue). The brain compares the signals from the three types to build the sensation of colour. A colour vision deficiency occurs when one type of cone is missing, or when its sensitivity is shifted so that it overlaps too much with another.

The types

TypeWhat is affectedWhat it looks like
Protanomaly / protanopiaL cones shifted or missingReds look darker and less saturated; red can be confused with dark green, brown or black
Deuteranomaly / deuteranopiaM cones shifted or missingGreens and reds, and some browns, oranges and pinks, are confused
Tritanomaly / tritanopiaS cones shifted or missingBlues and greens, and yellows and pinks or violets, are confused (rare)
AchromatopsiaCone function absent or severely reducedLittle or no colour perception; often with poor acuity and light sensitivity (very rare)

The suffix "-anomaly" means the cone is present but shifted (a milder deficiency), and "-opia" means it is missing (more severe). Deuteranomaly is the most common deficiency overall.

How common is it?

Among people of Northern European descent, roughly 8% of men and 0.5% of women have a red-green deficiency (Birch, 2012). Rates are somewhat lower in many other populations. Tritan deficiencies are far rarer, with estimates of the order of 1 in several thousand people, and complete colour blindness is rarer still.

Why men are affected far more often

The genes for the L and M cone pigments sit on the X chromosome. Men have one X chromosome, so a single faulty copy produces a deficiency. Women have two, so they usually need faulty copies on both, although a woman who carries one faulty copy can pass it on to her sons. Tritan deficiency is carried on an autosome (chromosome 7) and affects men and women equally.

Acquired colour vision changes

Colour vision can also change later in life. Causes include eye diseases such as glaucoma, macular degeneration and diabetic retinopathy; neurological conditions; certain medications and chemical exposures; and the natural yellowing of the lens with age, which makes blues harder to discriminate. A sudden change in colour vision is a reason to see an eye professional.

How colour vision is tested

Our colour vision test is an arrangement test in the style of the Farnsworth-Munsell approach: you drag chips into a smooth progression of hue.

What an online test can and cannot tell you

A screen is not a calibrated instrument. The colours you see depend on the display, brightness, colour temperature and room lighting, so the same test can give different results on different devices. Turn off night mode and blue-light filters, use a bright screen and avoid glare. An online test can suggest a possible deficiency, and it can show roughly which part of the hue circle gives you trouble, but it cannot diagnose. If colour matters for your work or studies (aviation, electrical trades, some design and medical roles, and some armed services have colour vision requirements), get a clinical test.

Living with it

Sources

Try it yourself: Color Vision TestFree, no sign-up, results shown on this device.
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About the author. Eduard-Dragos Condria builds and maintains CoreSkillAI from Romania. He is a web developer, not a clinician. Articles are written from published research, cited at the end, and corrected when a reader or a source shows an error. See the methodology page and about page. To report a mistake, use the contact page. Nothing on this site is medical or psychological advice.
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