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    <!-- http://www.orpha.net/ORDO/Orphanet_31150 -->

    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_31150">
        <rdfs:label>obsolete_Tangier disease</rdfs:label>
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        <oboInOwl:hasDbXref>UMLS:C0039292</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>Tangier disease (TD) is a rare lipoprotein metabolism disorder characterized biochemically by an almost complete absence of plasma high-density lipoproteins (HDL), and clinically by liver, spleen, lymph node and tonsil enlargement along with peripheral neuropathy in children and adolescents, and, occasionally, cardiovascular disease in adults.</ns4:IAO_0000115>
        <oboInOwl:hasExactSynonym>ATP-binding cassette transporter A1 deficiency</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:205400</oboInOwl:hasDbXref>
        <ns5:definition_citation>orphanet</ns5:definition_citation>
        <oboInOwl:hasDbXref>MESH:D013631</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Defective adenosine triphosphate-binding cassette transporter A1</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Analphalipoproteinemia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICD10:E78.6</oboInOwl:hasDbXref>
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