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

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005559">
        <rdfs:label>neurodegenerative disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015518 -->

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        <rdfs:label>infantile bilateral striatal necrosis</rdfs:label>
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        <oboInOwl:hasRelatedSynonym>striatal degeneration familial</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>striatonigral degeneration infantile</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>infantile striatonigral degeneration</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>Orphanet:1576</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>infantile striatonigral necrosis</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>infantile bilateral striatal necrosis</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C0795996</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>SNDI</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>NANDO:2200888</oboInOwl:hasDbXref>
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        <ns4:IAO_0000115>Several syndromes of bilateral symmetric spongy degeneration of the caudate nucleaus, putamen and globus pallidus characterized by developmental regression, choreoathetosis and dystonia progressing to spastic quadriparesis. IBSN can be familial or sporadic.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>GARD:0005040</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:167090</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:2100242</oboInOwl:hasDbXref>
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        <rdfs:label>obsolete rare genetic syndromic intellectual disability</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0017641 -->

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        <rdfs:label>obsolete miscellaneous movement disorder due to neurodegenerative disease</rdfs:label>
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        <rdfs:label>obsolete miscellaneous movement disorder due to genetic neurodegenerative disease</rdfs:label>
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