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| Term | blue color blindness | ID (Ontology) | DOID:11661 (Human Disease) |
| 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. | ||
| Also Known As | "Tritan defect" ; "Tritanopia" | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal genetic disease |__autosomal dominant disease__ blindness | |__color blindness_____________| blue color blindness |
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| Is a |
autosomal dominant disease color blindness |
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External Crossreferences & Linkouts
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ICD10CM:H53.55 ICD9CM:368.53 MESH:D003117 MIM:190900 SNOMEDCT_US_2023_03_01:51886007 UMLS_CUI:C0155017 |
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