Tritanopia

Description

Tritanopia is an extremely rare form of colour blindness characterised by a selective deficiency of blue vision.

Clinical Features

Phenotypes and symptoms related to Tritanopia

  • Optic atrophy
  • Confusion
  • Dyschromatopsia
  • Tritanomaly
  • Abnormal light-adapted electroretinogram

Incidence and onset information

— Based on the latest data available TRITANOPIA have a estimated prevalence of 4.8 per 100k worldwide.
No data available about the known clinical features onset.

Alternative names

Tritanopia Is also known as blue colorblindness, tritan colour blindness, blue colour blindness, colorblindness, tritanopic, congenital tritanopia, colorblindness, tritan, cbt.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Tritanopia Recommended genes panels

Panel Name, Specifity and genes Tested/covered
OPN1SW.

By Fulgent Genetics Fulgent Genetics (United States).

OPN1SW
Specificity
100 %
Genes
100 %

You can get up to -7 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

ORPHANET OMIM Rare Disease Search Engine

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