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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_disorder"/>
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    <!-- http://purl.obolibrary.org/obo/RO_0004003 -->

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        <rdf:type rdf:resource="http://www.w3.org/2002/07/owl#TransitiveProperty"/>
        <rdfs:label>has material basis in germline mutation in</rdfs:label>
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        <rdfs:label>disease has feature</rdfs:label>
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    <!-- http://identifiers.org/hgnc/869 -->

    <Class rdf:about="http://identifiers.org/hgnc/869">
        <rdfs:label>ATP7A</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/HP_0000499 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0000499">
        <rdfs:label>Abnormal eyelash morphology</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/HP_0000534 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0000534">
        <rdfs:label>Abnormal eyebrow morphology</rdfs:label>
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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_0002917 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0002917">
        <rdfs:label>disorder of pilosebaceous unit</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0004689 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0004689">
        <rdfs:label>inborn metal metabolism disorder</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0010651 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0010651">
        <rdfs:label>Menkes disease</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0002254"/>
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        </rdfs:subClassOf>
        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/4521</ns5:IAO_0000233>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/1521/menkes-disease</rdfs:seeAlso>
        <ns3:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/menkes_disease</ns3:curated_content_resource>
        <oboInOwl:hasExactSynonym>Menkes kinky hair syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Menkes syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0001521</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>menkes disease, X-linked recessive</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:309400</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>X-linked copper deficiency</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Menkes disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>NANDO:1200653</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D007706</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:44030</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>kinky hair syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICD9:759.89</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:1838</oboInOwl:hasDbXref>
        <ns5:IAO_0000115>A usually severe multisystemic disorder of copper metabolism, characterized by progressive neurodegeneration and marked connective tissue anomalies as well as typical sparse abnormal steely hair.</ns5:IAO_0000115>
        <oboInOwl:hasDbXref>MedDRA:10027294</oboInOwl:hasDbXref>
        <oboInOwl:hasBroadSynonym>copper transport disease</oboInOwl:hasBroadSynonym>
        <oboInOwl:hasExactSynonym>MNK</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Mk</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C0022716</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>steely hair disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>Menkea syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>Menkes kinky-hair syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>kinky hair disease</oboInOwl:hasExactSynonym>
        <oboInOwl:id>MONDO:0010651</oboInOwl:id>
        <oboInOwl:hasDbXref>Orphanet:565</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C75486</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NORD:1440</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:59178007</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:2200580</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>icd11.foundation:986728180</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Trichopoliodystrophy</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>MD</oboInOwl:hasExactSynonym>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0017762 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0017762">
        <rdfs:label>disorder of copper metabolism</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0019282 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019282">
        <rdfs:label>obsolete syndromic hair shaft abnormality</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0020189 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020189">
        <rdfs:label>obsolete eyebrow/eyelashes structural anomaly</rdfs:label>
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