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    <!-- http://purl.obolibrary.org/obo/MONDO_0005328 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005328">
        <rdfs:label>eye disorder</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015950 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015950">
        <rdfs:label>obsolete inherited skin tumor</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019300 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019300">
        <rdfs:label>obsolete rare skin tumor or hamartoma</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0019336 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019336">
        <rdfs:label>Gardner syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0005328"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0021055"/>
        <ns2:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/gardner_syndrome</ns2:curated_content_resource>
        <oboInOwl:hasDbXref>UMLS:C0017097</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Gardner syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MESH:D005736</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0019336</oboInOwl:id>
        <oboInOwl:hasDbXref>GARD:0006482</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C6728</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:60876000</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Gardner&#39;s syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>polyposis coli and multiple hard and soft tissue tumours</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>intestinal polyposis, osteomas, sebaceous cysts</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>MedDRA:10017727</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:6547</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>Gardner syndrome is a severe form of familial adenomatous polyposis characterized by multiple adenomas in the colon and rectum associated with prominent extracolonic features including osteomas and multiple skin and soft tissue tumors.</ns4:IAO_0000115>
        <oboInOwl:hasRelatedSynonym>polyposis coli and multiple hard and soft tissue tumors</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>icd11.foundation:1428130769</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:759.89</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:79665</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0020063 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020063">
        <rdfs:label>obsolete malformation syndrome with hamartosis</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0020176 -->

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        <rdfs:label>obsolete palpebral sebaceous gland tumor</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0021055 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0021055">
        <rdfs:label>classic familial adenomatous polyposis</rdfs:label>
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