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    <!-- http://purl.obolibrary.org/obo/MONDO_0000426 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000426">
        <rdfs:label>autosomal dominant disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0001516 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0001516">
        <rdfs:label>spinal muscular atrophy</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015362 -->

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        <rdfs:label>neuronopathy, distal hereditary motor, autosomal dominant</rdfs:label>
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        <oboInOwl:hasDbXref>Orphanet:140465</oboInOwl:hasDbXref>
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        <oboInOwl:hasExactSynonym>distal hereditary motor neuropathy, autosomal dominant</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:1787720</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0015362</oboInOwl:id>
        <oboInOwl:hasExactSynonym>autosomal dominant distal hereditary motor neuropathy</oboInOwl:hasExactSynonym>
        <ns3:IAO_0000115>Autosomal dominant form of distal hereditary motor neuropathy.</ns3:IAO_0000115>
        <oboInOwl:hasDbXref>UMLS:C5548212</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>OMIMPS:182960</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0018894 -->

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