About   Help   FAQ
Disease Ontology Browser
blue color blindness (DOID:11661)
Alliance: disease page
Synonyms: Tritan defect; Tritanopia
Alt IDs: OMIM:190900, ICD10CM:H53.55, ICD9CM:368.53, MESH:D003117, UMLS_CUI:C0155017
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.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
12/05/2017
MGI 6.11
The Jackson Laboratory