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    <!-- http://purl.obolibrary.org/obo/MONDO_0001336 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0001336">
        <rdfs:label>familial hyperlipidemia</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0008810 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0008810">
        <rdfs:label>familial apolipoprotein C-II deficiency</rdfs:label>
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        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015905"/>
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        <ns3:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/familial_apolipoprotein_c_ii_deficiency</ns3:curated_content_resource>
        <oboInOwl:hasDbXref>UMLS:C1720779</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>icd11.foundation:877401371</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:207750</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:309020</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>familial apoC-II deficiency</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>GARD:0000759</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:0111418</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:328375</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>hyperlipoproteinemia, type IB</oboInOwl:hasExactSynonym>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015905 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015905">
        <rdfs:label>syndromic dyslipidemia</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0018637 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0018637">
        <rdfs:label>familial chylomicronemia syndrome</rdfs:label>
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    <!-- http://www.orpha.net/ORDO/Orphanet_309020 -->

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        <rdfs:label>obsolete_familial apolipoprotein C-II deficiency</rdfs:label>
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