OBO ID: DOID:11661 |
Term Name: | blue color blindness | Search Ontology: | |
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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. (3) | ||
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Ontology: | Human Disease ( DOID:11661 ) |
OTHER blue color blindness PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS (1)
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