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Disease Ontology Browser
blue color blindness (DOID:11661)
Alliance: disease page
Synonyms: Tritan defect; Tritanopia
Alt IDs: OMIM:190900, ICD10CM:H53.55, ICD9CM_2006:368.53, 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 Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
01/31/2023
MGI 6.22
The Jackson Laboratory