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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000412"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0017773 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0017773">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">hypoalphalipoproteinemia</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0018999 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0018999">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">LCAT deficiency</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0017773"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0019743"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0020279"/>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">ICD10:E78.6</oboInOwl:hasDbXref>
        <ns2:IAO_0000115 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">LCAT (lecithin-cholesterol acyltransferase) deficiency is a rare lipoprotein metabolism disorder characterized clinically by corneal opacities, and sometimes renal failure and hemolytic anemia, and biochemically by severely reduced HDL cholesterol.</ns2:IAO_0000115>
        <oboInOwl:id rdf:datatype="http://www.w3.org/2001/XMLSchema#string">MONDO:0018999</oboInOwl:id>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Orphanet:650</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref rdf:datatype="http://www.w3.org/2001/XMLSchema#string">SCTID:49227001</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym rdf:datatype="http://www.w3.org/2001/XMLSchema#string">lecithin-cholesterol acyltransferase deficiency</oboInOwl:hasExactSynonym>
        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/49227001"/>
        <skos:closeMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C0023195"/>
        <oboInOwl:inSubset rdf:resource="http://purl.oboInOwllibrary.org/oboInOwl/mondo#ordo_disease"/>
        <ns2:IAO_0000412 rdf:resource="http://purl.obolibrary.org/obo/mondo.owl"/>
        <skos:exactMatch rdf:resource="http://www.orpha.net/ORDO/Orphanet_650"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019743 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019743">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">nephropathy secondary to a storage or other metabolic disease</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0020279 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020279">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">metabolic disease with corneal opacity</rdfs:label>
    </Class>
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