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    <!-- 
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_disorder"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#otar"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_malformation_syndrome"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasRelatedSynonym"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000233"/>
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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_0008823 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0008823">
        <rdfs:label>arthrogryposis multiplex congenita 2, neurogenic type</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0015327 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015327">
        <rdfs:label>developmental anomaly of metabolic origin</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0017123 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0017123">
        <rdfs:label>arthrogryposis-renal dysfunction-cholestasis syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0002254"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0008823"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015327"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0017755"/>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6749</ns4:IAO_0000233>
        <oboInOwl:hasRelatedSynonym>arthrogryposis renal dysfunction cholestasis syndrome</oboInOwl:hasRelatedSynonym>
        <ns4:IAO_0000115>Arthrogryposis-Renal dysfunction-Cholestasis (ARC) syndrome is a multisystem disorder, characterized by neurogenic arthrogryposis multiplex congenita, renal tubular dysfunction and neonatal cholestasis with low serum gamma-glutamyl transferase activity.</ns4:IAO_0000115>
        <oboInOwl:id>MONDO:0017123</oboInOwl:id>
        <oboInOwl:hasDbXref>Orphanet:2697</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIMPS:208085</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:0050763</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C535382</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:1647210</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C4551984</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>ARC syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>arthrogryposis, renal dysfunction, and cholestasis</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0000794</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:720513002</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>arthrogryposis - renal dysfunction - cholestasis</oboInOwl:hasRelatedSynonym>
        <rdfs:comment>This term&#39;s classification was reviewed in the context of the Strategic Refinement project (2023) and was determined to be excluded from the &#39;integumentary system disorder&#39; (MONDO:0002051) ontology branch (https://orcid.org/0000-0001-9310-0163, https://orcid.org/0000-0003-4830-7530)</rdfs:comment>
        <oboInOwl:hasRelatedSynonym>arthrogryposis multiplex congenita, renal dysfunction, and cholestasis</oboInOwl:hasRelatedSynonym>
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        <skos:exactMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C4551984"/>
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        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
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        <skos:exactMatch rdf:resource="https://omim.org/phenotypicSeries/PS208085"/>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0017755 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0017755">
        <rdfs:label>inborn disorder of bilirubin metabolism</rdfs:label>
    </Class>
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