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    <!-- http://www.orpha.net/ORDO/Orphanet_181422 -->

    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_181422">
        <rdfs:label>Rare hyperlipidemia</rdfs:label>
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    <!-- http://www.orpha.net/ORDO/Orphanet_70470 -->

    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_70470">
        <rdfs:label>Hyperlipoproteinemia type 5</rdfs:label>
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        <oboInOwl:hasDbXref>ICD10:E78.3</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>familial type 5 hyperlipoproteinemia (disorder)</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:144650</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Fredrickson type V lipaemia</oboInOwl:hasExactSynonym>
        <ns2:IAO_0000115>A severe type of hyperlipidemia, sometimes familial, that is characterized by the elevation of both plasma CHYLOMICRONS and TRIGLYCERIDES contained in VERY-LOW-DENSITY LIPOPROTEINS. Type V hyperlipoproteinemia is often associated with DIABETES MELLITUS and is not caused by reduced LIPOPROTEIN LIPASE activity as in HYPERLIPOPROTEINEMIA TYPE I .</ns2:IAO_0000115>
        <oboInOwl:hasDbXref>MedDRA:10060755</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Major hyperlipidemia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>hyperlipoproteinemia type V</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MESH:D006954</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0020481</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Hyperlipoproteinemia Type V</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>DOID:1171</oboInOwl:hasDbXref>
        <ns2:IAO_0000117>Sirarat Sarntivijai</ns2:IAO_0000117>
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