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    <!-- http://purl.obolibrary.org/obo/MONDO_0013091 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0013091">
        <rdfs:label>glycogen storage disease IXc</rdfs:label>
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        <oboInOwl:hasExactSynonym>glycogen storage disease IXc</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>NANDO:1200849</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>A liver PhK deficiency caused by variants in the PHKG2 gene</ns3:IAO_0000115>
        <oboInOwl:hasExactSynonym>GSD type IXc</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>PHKG2 glycogen storage disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:613027</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C2751643</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>GSD9C</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>glycogen storage disease caused by mutation in PHKG2</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MESH:C567809</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:442778</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0018387</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0013091</oboInOwl:id>
        <oboInOwl:hasExactSynonym>PHKG2-related glycogen storage disease type IX</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>NANDO:2201166</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>glycogen storage disease type IXc</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>GSD type 9C</oboInOwl:hasExactSynonym>
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