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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#disease_grouping"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#otar"/>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000233"/>
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    <!-- http://purl.obolibrary.org/obo/RO_0004020 -->

    <ObjectProperty rdf:about="http://purl.obolibrary.org/obo/RO_0004020">
        <rdfs:label>disease has basis in dysfunction of</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/CL_0000573 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/CL_0000573">
        <rdfs:label>retinal cone cell</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0001703 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0001703">
        <rdfs:label>color vision disorder</rdfs:label>
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        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/9097</ns5:IAO_0000233>
        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/9285</ns5:IAO_0000233>
        <ns3:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/color_blindness</ns3:curated_content_resource>
        <oboInOwl:hasDbXref>Orphanet:98658</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>color blindness</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>colour vision defects</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>blindness color</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>blindness colour</oboInOwl:hasExactSynonym>
        <oboInOwl:id>MONDO:0001703</oboInOwl:id>
        <oboInOwl:hasDbXref>ICD10CM:H53.5</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:193683001</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:1826147</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:368.5</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:13399</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C3891</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>color vision defects</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICD9:368.59</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>color vision deficiency</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C5681659</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>color-vision disease</oboInOwl:hasExactSynonym>
        <ns5:IAO_0000115>The absence of or defect in the perception of colors.</ns5:IAO_0000115>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0001941 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0001941">
        <rdfs:label>blindness (disorder)</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0021084 -->

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        <rdfs:label>vision disorder</rdfs:label>
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