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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- http://purl.obolibrary.org/obo/HP_0012373 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0012373">
        <rdfs:label>Abnormal eye physiology</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/HP_0030637 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0030637">
        <rdfs:label>Congenital stationary cone dysfunction</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/HP_0012373"/>
        <oboInOwl:hasDbXref>UMLS:C0543968</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Cone dysfunction syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Cone dysfunction</oboInOwl:hasExactSynonym>
        <ns3:IAO_0000115>Retinal phenotype characterized by cone photoreceptor dysfunction and preserved rod system. The abnormality is typically stationary or very slowly progressive and findings may include reduced central vision, color vision abnormalities, nystagmus and photophobia.</ns3:IAO_0000115>
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