Human genes for blue cone monochromacy
Blue cone monochromacy [DOID:0050679]
An achromatopsia that is characterized by severely impaired color discrimination, low visual acuity, nystagmus, photophobia due to the absence of functional long wavelength-sensitive and medium wavelength-sensitive cones in the retina and has_material_basis_in recessive X-linked inheritance.
Synonyms: blue cone monochromacy, blue cone monochromacies, DOID:0050679
Linkouts: OMIM