blue color blindness

Summary

DOID:11661 - blue color blindness

Disease Ontology 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.

Synonyms: Tritan defect, Tritanopia,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: opn1sw

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0008610 - blue color blindness

MONDO:0008610 - blue color blindness

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), color blindness (is_a)