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Echinobase
Summary Literature (0)
DOID:11661 - blue color blindness

Disease Ontology Definition:A color blindness that is characterised 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.

Synonyms: Tritan defect, Tritanopia,

Echinobase Genes :


OMIM:
MIM:190900 - tritanopia

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): color blindness (is_a)