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    <!-- http://purl.obolibrary.org/obo/MONDO_0000014 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000014">
        <rdfs:label>colorblindness, partial</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0010564 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0010564">
        <rdfs:label>red-green color blindness</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0000014"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0100545"/>
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        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/colorblindness_partial_deutan_series</ns4:curated_content_resource>
        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/red_green_color_blindness</ns4:curated_content_resource>
        <ns3:IAO_0000115>Deuteranopia is a type of color vision deficiency where the green photoreceptors are absent. It affects hue discrimination in the same way as protanopia, but without the dimming effect. Like protanopia, it is hereditary, sex-linked, and found in about 1% of the male population.</ns3:IAO_0000115>
        <oboInOwl:hasDbXref>Orphanet:319698</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:13909</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:102324</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:303800</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>CBD</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>partial achromatopsia, deutan type</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICD10CM:H53.53</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:77479002</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0155016</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0010564</oboInOwl:id>
        <oboInOwl:hasDbXref>GARD:0027795</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>deuteranopia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Deutan defect</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICD9:368.52</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>colorblindness, partial, DEUTAN series</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>colorblindness, deutan</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>EFO:0005581</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0100545 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0100545">
        <rdfs:label>hereditary neurological disease</rdfs:label>
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    <!-- http://www.ebi.ac.uk/efo/EFO_0005581 -->

    <Class rdf:about="http://www.ebi.ac.uk/efo/EFO_0005581">
        <rdfs:label>obsolete_red-green color blindness</rdfs:label>
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