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    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015548">
        <rdfs:label>Huntington disease-like syndrome</rdfs:label>
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    <!-- http://www.orpha.net/ORDO/Orphanet_207018 -->

    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_207018">
        <rdfs:label>Rare hereditary metabolic disease with peripheral neuropathy</rdfs:label>
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    <!-- http://www.orpha.net/ORDO/Orphanet_2388 -->

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        <rdfs:label>Choreoacanthocytosis</rdfs:label>
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        <ns3:IAO_0000115>Chorea-acanthocytosis (ChAc) is a form of neuroacanthocytosis (see this term) and is characterized clinically by a Huntington disease-like phenotype with progressive neurological symptoms including movement disorders, psychiatric manifestations and cognitive disturbances.</ns3:IAO_0000115>
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        <oboInOwl:hasExactSynonym>Levine-Critchley syndrome</oboInOwl:hasExactSynonym>
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        <rdfs:label>Miscellaneous movement disorder due to genetic neurodegenerative disease</rdfs:label>
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        <rdfs:label>Other genetic epidermal disease</rdfs:label>
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