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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_0005039 -->

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        <rdfs:label>reproductive system disorder</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0008305 -->

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        <rdfs:label>Currarino triad</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/6751</ns3:IAO_0000233>
        <ns3:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6753</ns3:IAO_0000233>
        <ns3:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6877</ns3:IAO_0000233>
        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/currarino_syndrome</ns4:curated_content_resource>
        <oboInOwl:hasDbXref>MESH:C536221</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>partial sacral agenesis with intact first sacral vertebra, presacral mass and anorectal malformation</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>GARD:0001626</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:759.89</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:413936007</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Currarino triad</oboInOwl:hasExactSynonym>
        <ns3:IAO_0000115>Currarino syndrome (CS) is a rare congenital disease characterized by the triad of anorectal malformations (ARMs) (usually anal stenosis), presacral mass (commonly anterior sacral meningocele (ASM) or teratoma) and sacral anomalies (i.e. total or partial agenesis of the sacrum and coccyx or deformity of the sacral vertebrae).</ns3:IAO_0000115>
        <oboInOwl:hasDbXref>DOID:0111546</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:176450</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>icd11.foundation:1532133816</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:1552</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C1531773</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Currarino syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:323460</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0018230 -->

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        <rdfs:label>skeletal dysplasia</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0018234 -->

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        <rdfs:label>dysostosis</rdfs:label>
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