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Living with Blue color blindness

An extremely rare inherited condition in which blue colors are hard to see.

Understanding Blue color blindness

Blue color blindness, also called tritanopia, is an extremely rare form of color blindness with a lack of blue vision.

It is present from newborn and infant years. Color vision tests are abnormal. Some people may also have less clear vision, light sensitivity, or rhythmic eye movements.

Signs & symptoms

Symptoms vary from person to person. GARD lists these among the most common:

  • Trouble telling blue and yellow apart
  • Abnormal color vision test
  • Changes in the retina

Not everyone has every symptom. GARD's list comes from the Human Phenotype Ontology.

Diagnosis

  1. Talk with your doctor

    Share the symptoms you've noticed, when they started and your family health history. Notes and photos can help.

  2. See a specialist

    Specialists who may be involved include eye disease specialists and genetic specialists.

  3. Consider genetic testing

    Changes in OPN1SW are linked to this condition. Genetic testing and counseling can help confirm a diagnosis and explain what it means for your family.

Care & treatment

Care team
Eye disease specialists (ophthalmologists); Genetic specialists (geneticists)
Expert care
Ask about multidisciplinary care centers for rare conditions
Treatment
GARD doesn't list specific treatments for this condition. Your care team will tailor care to your symptoms.
Research
Clinical trials and observational studies may be options. See the research section below.

General information, not medical advice. Your care team makes the decisions.

Everyday life

Living with a rare condition is easier with support.

  • Connect with Prevent Blindness America
  • Keep notes on symptoms, changes and questions for appointments
  • Ask about patient registries that help research
  • Look into financial aid and travel resources for care visits
Bring these questions to your next doctor visit
Which color vision tests can confirm this type?
Can OPN1SW gene testing be done?
Do I need other eye checks?

Quick facts

Symptoms usually startNewborn and as an Infant
InheritanceAutosomal Dominant
GenesOPN1SW

Changes in the OPN1SW gene cause this condition. It is autosomal dominant, so one changed copy of the gene is enough.

Genetic

Also known as: blue colorblindness; blue colour blindness; blue yellow color blindness; blue yellow colour blindness; blue-yellow dyschromatopsia; blue/yellow color vision defect

Patient organizations

Source: NIH GARD · Blue color blindnessGARD ID 16768 · GARD page updated September 2026 · Plain-language summary by Know Rare; editorial review pending. General information, not medical advice.

You are more than your diagnosis

Perspectives from people navigating life with Blue color blindness.

Explore the Blue color blindness blog

Explore research for Blue color blindness

Explore actively recruiting Blue color blindness studies with HealthSpark.

HealthSpark

Find actively recruiting studies for Blue color blindness with HealthSpark. Share your city to explore research near you.

  • Recruiting studies from ClinicalTrials.gov
  • Share your city to look for research near you
  • Eligibility is confirmed by the study team

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I can help you find recruiting Blue color blindness studies. Enter a ZIP code, address or city below and I'll look within 50 miles.

Powered by HealthSpark, our AI chat helper · Study information from ClinicalTrials.gov · Eligibility is confirmed by the study team.

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