Congenital stationary night blindness, TRPM1-related, horse
MONDO:1011255Non-progressive vision impairment in dim or absent lighting in horses due to a variation in the TRPM1 gene. Specifically, horses homozygous for a white spotting phenotype, known as leopard complex spotting, are affected by CSNB.
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Disease
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Congenital blindness, non-human animal
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Disorder of visual system, non-human animal
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Hereditary disease, non-human animal
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Nervous system disorder, non-human animal
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Non-human animal disease
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Perceptual disorders, non-human animal
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Vision disorder, non-human animal
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