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    <!-- http://purl.obolibrary.org/obo/MONDO_0020248 -->

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    <!-- http://purl.obolibrary.org/obo/MONDO_0100288 -->

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        <ns3:IAO_0000115>An autosomal recessive retinopathy in which patients have increased sensitivity to blue light; perception of blue light is mediated by what is normally the least populous cone photoreceptor subtype, the S (short wavelength, blue) cones. Characteristics include visual loss, with night blindness occurring from early in life, varying degrees of L (long, red)- and M (middle, green)-cone vision, and retinal degeneration.</ns3:IAO_0000115>
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