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    <!-- http://purl.obolibrary.org/obo/MONDO_0000425 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000425">
        <rdfs:label>X-linked disease</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0003847"/>
        <disjointWith rdf:resource="http://purl.obolibrary.org/obo/MONDO_0000426"/>
        <disjointWith rdf:resource="http://purl.obolibrary.org/obo/MONDO_0006025"/>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/8550</ns4:IAO_0000233>
        <oboInOwl:hasExactSynonym>X-linked disease or disorder</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>disease, X-linked genetic</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>ICD9:799.89</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>diseases, X-linked genetic</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>X-linked genetic diseases</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>X-linked inherited disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>NCIT:C85865</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0000425</oboInOwl:id>
        <oboInOwl:hasDbXref>DOID:0050735</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C1138434</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:222910</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>X-linked form of disease.</ns4:IAO_0000115>
        <oboInOwl:hasExactSynonym>X-linked hereditary disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>genetic diseases, X chromosome linked</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>SCTID:128430005</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>X-linked genetic disease</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>genetic diseases, X-chromosome linked</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>MESH:D040181</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>genetic diseases, X linked</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>disease, X-linked</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>X-linked inherited disorder</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>X linked genetic diseases</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>disease or disorder, X-linked</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>genetic disease, X-linked</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>X-linked hereditary disorder</oboInOwl:hasExactSynonym>
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        <skos:exactMatch rdf:resource="http://linkedlifedata.com/resource/umls/id/C1138434"/>
        <skos:exactMatch rdf:resource="http://purl.obolibrary.org/obo/DOID_0050735"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0000426 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000426">
        <rdfs:label>autosomal dominant disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0003847 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0003847">
        <rdfs:label>hereditary disease</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0006025 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0006025">
        <rdfs:label>autosomal recessive disease</rdfs:label>
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