Tritanopia is an extremely rare form of colour blindness characterised by a selective deficiency of blue vision.
Genes related to Tritanopia
Clinical FeaturesPhenotypes and symptoms related to Tritanopia
- Optic atrophy
- 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.
Tritanopia Is also known as blue colorblindness, tritan colour blindness, blue colour blindness, colorblindness, tritanopic, congenital tritanopia, colorblindness, tritan, cbt.
Researches and researchersCurrently, 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|
By Fulgent Genetics Fulgent Genetics (United States).
You can get up to -7 more panels with our dedicated toolLearn more
Sources and references
You can check the following sources for additional information.ORPHANET OMIM Rare Disease Search Engine
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