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Congenital red–green color blindness is an inherited condition that is the root cause of the majority of cases of color blindness. It has no significant symptoms aside from its minor to moderate effect on color vision. It is caused by variation in the functionality of the red and/or green opsin proteins, which are the photosensitive pigment in the cone…
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| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Congenital red–green color blindness | Causes | Genetic (inherited, usually X-linked) | 1.00 | infobox |
| Congenital red–green color blindness | Diagnostic method | Color vision tests | 1.00 | infobox |
| Congenital red–green color blindness | Differential diagnosis | Acquired red–green color blindness | 1.00 | infobox |
| Congenital red–green color blindness | Duration | Lifelong | 1.00 | infobox |
| Congenital red–green color blindness | Frequency | 2-9% males; <1% females | 1.00 | infobox |
| Congenital red–green color blindness | Medication | None | 1.00 | infobox |
| Congenital red–green color blindness | Other names | Daltonism; red–green color vision deficiency | 1.00 | infobox |
| Congenital red–green color blindness | Specialty | Ophthalmology | 1.00 | infobox |
| Congenital red–green color blindness | Symptoms | Reduced color distinction along red-green axis | 1.00 | infobox |
| Congenital red–green color blindness | Treatment | None | 1.00 | infobox |
| Congenital red–green color blindness | Usual onset | Congenital | 1.00 | infobox |
| Congenital red–green color blindness | is a | inherited condition that is the root cause of the majority of cases of color blindness | 0.90 | text |
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