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    <!-- http://purl.obolibrary.org/obo/MONDO_0005144 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005144">
        <rdfs:label>familial amyotrophic lateral sclerosis</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0014640 -->

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        <rdfs:label>frontotemporal dementia and/or amyotrophic lateral sclerosis 3</rdfs:label>
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        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0800464"/>
        <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:0016113</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:897127</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>frontotemporal dementia and/or amyotrophic lateral sclerosis 3</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:616437</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>FTDALS3</oboInOwl:hasExactSynonym>
        <ns3:IAO_0000115>An amyotrophic lateral sclerosis that has material basis in mutation in the SQSTM1 gene on chromosome 5q35.</ns3:IAO_0000115>
        <oboInOwl:hasExactSynonym>frontotemporal dementia and/or amyotrophic lateral sclerosis type 3</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C4225326</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:0110068</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0014640</oboInOwl:id>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0017160 -->

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        <rdfs:label>behavioral variant of frontotemporal dementia</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0017161 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0017161">
        <rdfs:label>frontotemporal dementia with motor neuron disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0030923 -->

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        <rdfs:label>frontotemporal dementia and/or amyotrophic lateral sclerosis</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0800464 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0800464">
        <rdfs:label>SQSTM1-related multisystem proteinopathy</rdfs:label>
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