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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_malformation_syndrome"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasDbXref"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasRelatedSynonym"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000233"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#id"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0006012"/>
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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>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0008666 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0008666">
        <rdfs:label>volvulus of midgut</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0016583 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0016583">
        <rdfs:label>familial intestinal malrotation-facial anomalies syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0002254"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0008666"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0021147"/>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6876</ns4:IAO_0000233>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6878</ns4:IAO_0000233>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/7700</ns4:IAO_0000233>
        <ns4:IAO_0006012>2024-09-01</ns4:IAO_0006012>
        <oboInOwl:hasRelatedSynonym>intestinal malrotation facial anomalies familial type</oboInOwl:hasRelatedSynonym>
        <rdfs:comment>Reason of obsoletion: out of scope - MONDO:excludeHistoricalDisease. Term to consider: -</rdfs:comment>
        <oboInOwl:hasDbXref>Orphanet:2454</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>Stalker Chitayat syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:id>MONDO:0016583</oboInOwl:id>
        <oboInOwl:hasExactSynonym>Stalker-Chitayat syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#inferred_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#obsoletion_candidate"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#ordo_malformation_syndrome"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#rare"/>
        <ns2:excluded_from_qc_check rdf:resource="http://purl.obolibrary.org/obo/mondo/sparql/qc/general/qc-single-child.sparql"/>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0021147 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0021147">
        <rdfs:label>disorder of development or morphogenesis</rdfs:label>
    </Class>
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