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    <!-- http://purl.obolibrary.org/obo/RO_0004029 -->

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        <rdfs:label>disease has feature</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0000209 -->

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        <rdfs:label>prenatal-onset spinal muscular atrophy with congenital bone fractures</rdfs:label>
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        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015168"/>
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        <oboInOwl:hasExactSynonym>spinal muscular atrophy with congenital bone fractures</oboInOwl:hasExactSynonym>
        <oboInOwl:id>MONDO:0000209</oboInOwl:id>
        <oboInOwl:hasDbXref>MEDGEN:1798941</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C5567518</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:486811</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0017882</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>SMABF</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIMPS:616866</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0001516 -->

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        <rdfs:label>spinal muscular atrophy</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0002320 -->

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        <rdfs:label>congenital nervous system disorder</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015168 -->

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        <rdfs:label>arthrogryposis multiplex congenita</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0024257 -->

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        <rdfs:label>hereditary motor neuron disease</rdfs:label>
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