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    <!-- http://purl.obolibrary.org/obo/MONDO_0008215 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0008215">
        <rdfs:label>adult-onset autosomal dominant demyelinating leukodystrophy</rdfs:label>
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        <oboInOwl:hasExactSynonym>leukodystrophy, adult-onset, autosomal dominant</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0010587</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>autosomal dominant leukodystrophy with autonomic disease</oboInOwl:hasRelatedSynonym>
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        <oboInOwl:hasRelatedSynonym>autosomal dominant adult-onset demyelinating leukodystrophy</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>Orphanet:99027</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C566813</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>multiple sclerosis-like disorder</oboInOwl:hasRelatedSynonym>
        <oboInOwl:id>MONDO:0008215</oboInOwl:id>
        <oboInOwl:hasDbXref>OMIMPS:169500</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DECIPHER:59</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>adult-onset autosomal dominant leukodystrophy</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>UMLS:C1868512</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:0060785</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>A rare, slowly progressive neurological disorder involving central nervous system demyelination, leading to autonomic dysfunction, ataxia and mild cognitive impairment.</ns3:IAO_0000115>
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        <oboInOwl:hasDbXref>SCTID:448054001</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016956 -->

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        <rdfs:label>partial trisomy of the long arm of chromosome 5</rdfs:label>
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        <rdfs:label>laminopathy</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0976138 -->

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