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Definition: impaired but not absent color vision with less severely reduced visual acuity than in complete achromatopsia, associated with photophobia and nystagmus; autosomal recessive inheritance. An autosomal dominant [MIM*180020] form and several X-linked [MIM*304020, MIM*300085, and MIM*303700] forms exist.
Examples: glitazone, GI cocktail, etc.
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