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    <!-- http://purl.obolibrary.org/obo/MONDO_0019052 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019052">
        <rdfs:label>inborn errors of metabolism</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0021179 -->

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        <rdfs:label>proteostasis deficiencies</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0800464 -->

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        <rdfs:label>SQSTM1-related multisystem proteinopathy</rdfs:label>
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        <ns3:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6882</ns3:IAO_0000233>
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        <oboInOwl:hasDbXref>GARD:0026565</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0800464</oboInOwl:id>
        <ns3:IAO_0000115>A group of disorders including Paget disease of bone (PBD), inclusion body myopathy (IBM), and less frequently frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS). Phenotypic presentation and severity are highly variable, and individuals within the same family may present with different associated conditions.</ns3:IAO_0000115>
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