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Up to: Retinal disorder · Color vision disorder
Achromatopsia
Achromatopsia (ACHM) is a rare autosomal recessive retinal disorder characterized by color blindness, nystagmus, photophobia, and severely reduced visual acuity due to the absence or impairment of cone function.
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Blue cone monochromacy 2 trials
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Achromatopsia 7 1 trial
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Achromatopsia 2 0 trials
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Achromatopsia 3 0 trials
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Achromatopsia 4 0 trials
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Achromatopsia 6 0 trials