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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: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.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.11
The Jackson Laboratory