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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_disorder"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0001627 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0001627">
        <rdfs:label>dementia</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0018591 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0018591">
        <rdfs:label>ITM2B amyloidosis</rdfs:label>
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        <oboInOwl:hasDbXref>MEDGEN:82800</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>ITM2B-related amyloidosis</oboInOwl:hasExactSynonym>
        <oboInOwl:id>MONDO:0018591</oboInOwl:id>
        <oboInOwl:hasExactSynonym>ITM2B-related cerebral amyloid angiopathy</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C0268393</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:439254</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>icd11.foundation:503091580</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0017741</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:277.39</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:45639009</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>familial cerebral amyloid angiopathy</oboInOwl:hasExactSynonym>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0018634 -->

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        <rdfs:label>hereditary amyloidosis</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0024237 -->

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        <rdfs:label>inherited neurodegenerative disorder</rdfs:label>
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