OBO ID: DOID:13911 |
Term Name: | achromatopsia | Search Ontology: | |
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Definition: | A color blindness that is characterized by a congenital cone color vision disorder, the inability to perceive color and to achieve satisfactory visual acuity at high light levels has_material_basis_in autosomal recessive inheritance. (4) | ||
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Ontology: | Human Disease ( DOID:13911 ) |
OTHER achromatopsia PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
Fish | Conditions | Citations |
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gnat2w21/w21 (AB) | standard conditions | Kennedy et al., 2007 |
PHENOTYPE
No data available
CITATIONS (2)
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