blue color blindness

Summary
Synonym
  • Tritan defect
  • Tritanopia
Definition
A color blindness that is characterized by a selective deficiency of blue vision, has_material_basis_in autosomal dominant inheritance of a mutation in the OPN1SW gene and is associated with a deficiency or absence of blue-sensitive cone photoreceptor function.
Super Class
autosomal dominant disease color blindness
Disease Ontology
DOID:11661
Mondo Disease Ontology
MeSH
UMLS
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
12057 Opn1sw opsin 1 (cone pigments), short-wave-sensitive (color blindness, tritan)
Displaying 1 entry
Gene ID Gene Symbol Description Source
81644 Opn1sw opsin 1, short wave sensitive
Displaying 1 entry
Gene ID Gene Symbol Description Source
30582 opn1sw1 opsin 1 (cone pigments), short-wave-sensitive 1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024