<?xml version="1.0"?>
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    <!-- 
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019234 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019234">
        <rdfs:label>peroxisome biogenesis disorder</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0100322 -->

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        <rdfs:label>non-Zellweger spectrum disorder</rdfs:label>
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        <ns3:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/2632</ns3:IAO_0000233>
        <ns3:IAO_0000115>A peroxisome biogenesis disorder which is due to defect in PEX7 or PEX5. This includes rhizomelic chondrodysplasia punctata due to defect in PEX7 or PEX5, and adult Refsum Disease due to defects in PEX7.</ns3:IAO_0000115>
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