Tritanopia

Tritanopia is an extremely rare hereditary condition corresponding to a loss in function of the short wavelength sensitive cones. To produce transient tritanopia, the eye of the normal observer is first strongly adapted to a yellow light that maximally adapts the pigment of the long and middle wavelength cones, but has relatively less influence on the short wavelength sensitive cones.

1997, M. Alpern, K. Kitahara, D. H. Krantz, 9: Perception of Colour in Unilateral Tritanopia, Alex Byrne, David R. Hilbert (editors), Readings on Color, Volume 2: The Science of Color, page 231, M. Alpern et. al 1983 gives results of colour matching and colour discrimination for each eye separately of a subject who acquired tritanopia in his left eye while remaining a normal trichromat with his right one.

People with an inborn blue-green blindness (tritanopia) may completely lack the function of these receptor cells.[…]The inheritance of inborn tritanopia is not sex-linked; the gene for the S-cone opsin is localized to chromosome 7.