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    <!-- http://purl.obolibrary.org/obo/MONDO_0015168 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015168">
        <rdfs:label>arthrogryposis multiplex congenita</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0025445 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0025445">
        <rdfs:label>Wieacker-Wolff syndrome (spectrum)</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015168"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0700223"/>
        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6461</ns5:IAO_0000233>
        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/7217</ns5:IAO_0000233>
        <oboInOwl:hasDbXref>OMIMPS:314580</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>ZARD</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>ZC4H2-associated rare disorders</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>ZC4H2-associated disorder</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0025477</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0025445</oboInOwl:id>
        <rdfs:comment>Grouping for the X-linked form seen mostly in males and female-restricted</rdfs:comment>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0700223 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0700223">
        <rdfs:label>hereditary skeletal muscle disorder</rdfs:label>
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