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    <!-- 
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#disease_grouping"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_group_of_disorders"/>
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    <!-- http://purl.obolibrary.org/obo/RO_0004022 -->

    <ObjectProperty rdf:about="http://purl.obolibrary.org/obo/RO_0004022">
        <rdfs:label>disease arises from feature</rdfs:label>
        <rdfs:label>disease has basis in feature</rdfs:label>
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        <rdfs:label>disease has major feature</rdfs:label>
    </ObjectProperty>
    


    <!-- 
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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>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0002279 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0002279">
        <rdfs:label>iron metabolism disease</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0002283 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0002283">
        <rdfs:label>neuroaxonal dystrophy</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0005395 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005395">
        <rdfs:label>movement disorder</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0005559 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005559">
        <rdfs:label>neurodegenerative disease</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0015547 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015547">
        <rdfs:label>hereditary dementia</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0018307 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0018307">
        <rdfs:label>neurodegeneration with brain iron accumulation</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0002279"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0002283"/>
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        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015547"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0019052"/>
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                <someValuesFrom rdf:resource="http://purl.obolibrary.org/obo/MONDO_0001627"/>
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        </rdfs:subClassOf>
        <ns5:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/neurodegeneration_with_brain_iron_accumulation</ns5:curated_content_resource>
        <ns4:IAO_0000115>Neurodegeneration with brain iron accumulation (NBIA, formerly Hallervorden-Spatz syndrome) encompasses a group of rare neurodegenerative disorders characterized by progressive extrapyramidal dysfunction (dystonia, rigidity, choreoathetosis), iron accumulation in the brain and the presence of axonal spheroids, usually limited to the central nervous system.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>MEDGEN:444156</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>icd11.foundation:440483530</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:0110734</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0018307</oboInOwl:id>
        <oboInOwl:hasDbXref>NANDO:2100241</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIMPS:234200</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:385</oboInOwl:hasDbXref>
        <rdfs:comment>Editor note: check relationship to PKAN</rdfs:comment>
        <oboInOwl:hasDbXref>GARD:0011899</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>neurodegeneration with brain iron accumulation</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C2931845</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C538421</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>NBIA</oboInOwl:hasExactSynonym>
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        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
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        <skos:exactMatch rdf:resource="http://www.orpha.net/ORDO/Orphanet_385"/>
        <skos:exactMatch rdf:resource="https://omim.org/phenotypicSeries/PS234200"/>
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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>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0024237 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0024237">
        <rdfs:label>inherited neurodegenerative disorder</rdfs:label>
    </Class>
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<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



