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    <!-- http://purl.obolibrary.org/obo/DOID_12858 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/DOID_12858">
        <rdfs:label>Huntington&#39;s disease</rdfs:label>
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        <oboInOwl:hasDbXref>ICD10CM:G10</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>MESH:D006816</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9CM:333.4</oboInOwl:hasDbXref>
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        <oboInOwl:hasExactSynonym xml:lang="en">HD</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym xml:lang="en">Huntington disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:143100</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS_CUI:C0020179</oboInOwl:hasDbXref>
        <ns2:IAO_0000115>A neurodegenerative disease that has_material_basis_in autosomal dominant inheritance and is characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia and has_material_basis_in expansion of CAG triplet repeats (glutamine) resulting in neuron degeneration affecting muscle coordination, cognitive abilities.</ns2:IAO_0000115>
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