<?xml version="1.0"?>
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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"/>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- 
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    //
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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_0005087 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005087">
        <rdfs:label>respiratory system disorder</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0005308 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005308">
        <rdfs:label>ciliopathy</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0016575 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0016575">
        <rdfs:label>primary ciliary dyskinesia</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0002254"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0005087"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0005308"/>
        <ns2:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/kartagener_syndrome</ns2:curated_content_resource>
        <ns2:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/primary_ciliary_dyskinesia</ns2:curated_content_resource>
        <oboInOwl:hasDbXref>MESH:D007619</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>icd11.foundation:1713839459</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MedDRA:10069713</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D002925</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:0050144</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>Siewert syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>DOID:9562</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:86204009</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIMPS:244400</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>Primary ciliary dyskinesia, Kartagener type</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>SCTID:42402006</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>Dextrocardia-bronchiectasis-sinusitis syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>Immotile cilia syndrome, Kartagener type</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>NORD:1605</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:3467</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>PCD</oboInOwl:hasExactSynonym>
        <rdfs:comment>Editor note: we deliberately merge two MESHes here</rdfs:comment>
        <oboInOwl:hasDbXref>NANDO:2200204</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:2100034</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0008780</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>ciliary dyskinesia primary</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>NCIT:C84797</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:2200203</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:244</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0004484</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>Primary ciliary dyskinesia and situs inversus</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>bronchiectasis, chronic sinusitis and dextrocardia syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:id>MONDO:0016575</oboInOwl:id>
        <oboInOwl:hasExactSynonym>Kartagener syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>Dextrocardia bronchiectasis and sinusitis</oboInOwl:hasRelatedSynonym>
        <ns4:IAO_0000115>A rare, genetically heterogeneous, primarily respiratory disorder characterized by chronic upper and lower respiratory tract disease. Approximately half of PCD patients have an organ laterality defect (situs inversus totalis or situs ambiguus/heterotaxy).</ns4:IAO_0000115>
        <oboInOwl:hasRelatedSynonym>ICS</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>Kartagener&#39;s syndrome</oboInOwl:hasExactSynonym>
        <skos:exactMatch rdf:resource="http://id.who.int/icd/entity/1713839459"/>
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        <skos:exactMatch rdf:resource="http://identifiers.org/mesh/D007619"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/42402006"/>
        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/86204009"/>
        <skos:exactMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C0008780"/>
        <skos:exactMatch rdf:resource="http://purl.obolibrary.org/obo/DOID_0050144"/>
        <skos:exactMatch rdf:resource="http://purl.obolibrary.org/obo/DOID_9562"/>
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        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#clingen"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#doid_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#ncit_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#nord_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#ordo_disorder"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#orphanet_rare"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#otar"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#rare"/>
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        <skos:exactMatch rdf:resource="http://www.orpha.net/ORDO/Orphanet_244"/>
        <skos:exactMatch rdf:resource="https://omim.org/phenotypicSeries/PS244400"/>
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    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0018395 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0018395">
        <rdfs:label>obsolete male infertility due to sperm motility disorder</rdfs:label>
    </Class>
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<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



