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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#otar"/>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_malformation_syndrome"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- http://purl.obolibrary.org/obo/RO_0004029 -->

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        <rdfs:label>disease has feature</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/HP_0004349 -->

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        <rdfs:label>Reduced bone mineral density</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0002254 -->

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        <rdfs:label>syndromic disease</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0017199 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0017199">
        <rdfs:label>osteoporosis-macrocephaly-blindness-joint hyperlaxity syndrome</rdfs:label>
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        <oboInOwl:hasDbXref>SCTID:716189005</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Heide syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>Orphanet:2787</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0018778</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0017199</oboInOwl:id>
        <ns5:IAO_0000115>Osteoporosis-macrocephaly-blindness-joint hyperlaxity syndrome is characterized by osteoporosis, macrocephalus, brachytelephalangy, and hyperextensibility of the joints. Congenital amaurosis and intellectual deficit have also been reported. This syndrome has been described in three members of one family.</ns5:IAO_0000115>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019704 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019704">
        <rdfs:label>obsolete primary bone dysplasia with decreased bone density</rdfs:label>
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