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    <!-- http://purl.obolibrary.org/obo/MONDO_0002254 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0002254">
        <rdfs:label>syndromic disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0008262 -->

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        <rdfs:label>Poland syndrome</rdfs:label>
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        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0700223"/>
        <ns3:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/4948</ns3:IAO_0000233>
        <ns3:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6751</ns3:IAO_0000233>
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        <oboInOwl:hasDbXref>MESH:D011045</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:12961</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:173800</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:2911</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>icd11.foundation:1364451323</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:38371006</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:10822</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C85017</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Poland anomaly</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0007412</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Poland sequence</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MedDRA:10036007</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0008262</oboInOwl:id>
        <oboInOwl:hasRelatedSynonym>Poland&#39;s syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>unilateral defect of pectoralis muscle and syndactyly of the hand</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>NORD:1587</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0032357</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Poland syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICD9:756.89</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>Poland syndrome is marked by a unilateral absence or hypoplasia of the pectoralis major muscle (most frequently involving the sternocostal portion), and a variable degree of ipsilateral hand anomalies, including symbrachydactyly.</ns3:IAO_0000115>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015856 -->

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        <rdfs:label>syndromic breast hypoplasia/aplasia</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019054 -->

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        <rdfs:label>congenital limb malformation</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019713 -->

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        <rdfs:label>non-syndromic limb reduction defect</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0700223 -->

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        <rdfs:label>hereditary skeletal muscle disorder</rdfs:label>
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