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    <!-- http://purl.obolibrary.org/obo/MONDO_0006025 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0006025">
        <rdfs:label>autosomal recessive disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0009999 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0009999">
        <rdfs:label>autosomal recessive Robinow syndrome</rdfs:label>
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        <ns3:IAO_0000115>Autosomal recessive Robinow syndrome (RRS) is the less common type of Robinow syndrome (RS) characterized by short-limb dwarfism, costovertebral segmentation defects and abnormalities of the head, face and external genitalia.</ns3:IAO_0000115>
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        <oboInOwl:hasExactSynonym>Robinow syndrome, autosomal recessive</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0016568</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>COVESDEM syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>costovertebral segmentation defect with mesomelia</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>RRS</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>Covesdem syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>OMIM:268310</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:1770070</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C535863</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C5399974</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019978 -->

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        <rdfs:label>Robinow syndrome</rdfs:label>
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        <rdfs:label>obsolete_autosomal recessive Robinow syndrome</rdfs:label>
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