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    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005180">
        <rdfs:label>Parkinson disease</rdfs:label>
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        <rdfs:label>Rare parkinsonian syndrome due to genetic neurodegenerative disease</rdfs:label>
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    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_411602">
        <rdfs:label>Hereditary late-onset Parkinson disease</rdfs:label>
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        <oboInOwl:hasExactSynonym>Autosomal dominant late-onset Parkinson disease</oboInOwl:hasExactSynonym>
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        <ns3:IAO_0000115>Hereditary late-onset Parkinson disease (LOPD) is a form of Parkinson disease (PD), characterized by an age of onset of more than 50 years, tremor at rest, gait complaints and falls, bradykinesia, rigidity and painful cramps. Patients usually present a low risk of developing non motor symptoms, dystonia, dyskinesia and levodopa-induced dyskinesia (LID).</ns3:IAO_0000115>
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