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    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_16">
        <rdfs:label>Blue cone monochromatism</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://www.orpha.net/ORDO/Orphanet_98658"/>
        <oboInOwl:hasExactSynonym>S cone monochromacy</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICD10:H53.5</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Blue cone monochromacy</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Color blindness, blue monocone monochromatic type</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MESH:C538165</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:303700</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Atypical X-linked achromatopsia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>S cone monochromatism</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Colour blindness, blue monocone monochromatic type</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>X-linked incomplete achromatopsia</oboInOwl:hasExactSynonym>
        <ns4:definition_citation>orphanet</ns4:definition_citation>
        <oboInOwl:hasDbXref>UMLS:C2931753</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>Blue cone monochromatism (BCM) is a recessive X-linked disease characterized by severely impaired color discrimination, low visual acuity, nystagmus, and photophobia, due to dysfunction of the red (L) and green (M) cone photoreceptors. BCM is as an incomplete form of achromatopsia (see this term).</ns3:IAO_0000115>
        <oboInOwl:hasDbXref>UMLS:C0339537</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C536238</oboInOwl:hasDbXref>
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