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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000233"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0002051 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0002051">
        <rdfs:label>integumentary system disorder</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0002082 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0002082">
        <rdfs:label>endocrine gland neoplasm</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0002123 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0002123">
        <rdfs:label>calcinosis</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0018891 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0018891">
        <rdfs:label>familial tumoral calcinosis</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0002051"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0002082"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0002123"/>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6749</ns4:IAO_0000233>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/10877/familial-tumoral-calcinosis</rdfs:seeAlso>
        <ns2:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/familial_tumoral_calcinosis</ns2:curated_content_resource>
        <oboInOwl:hasDbXref>GARD:0010877</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0263628</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>EFO:0009385</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0018891</oboInOwl:id>
        <oboInOwl:hasDbXref>Orphanet:53715</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>Tumoral calcinosis is a phosphocalcic metabolism anomaly, particularly among younger age groups and characterized by the presence of calcified masses in the juxta-articular regions (hip, elbow, ankle and scapula) without joint involvement. Histologically, lesions dysplay collagen necrobiosis, followed by cyst formation and a foreign-body response with calcification Two forms of tumoral calcinosis have been described: normocalcemic tumoral calcinosis and familial tumoral calcinosis.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>MEDGEN:452340</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MedDRA:10059364</oboInOwl:hasDbXref>
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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>
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