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    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_183570">
        <rdfs:label>Genetic malformation syndrome with short stature</rdfs:label>
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        <rdfs:label>3M syndrome</rdfs:label>
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        <oboInOwl:hasDbXref>UMLS:C1848862</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Yakut short stature syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Gloomy face syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICD10:Q87.1</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Dolichospondylic dysplasia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C1851996</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>MedDRA:10081775</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Le Merrer syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:273750</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:612921</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>3-M syndrome</oboInOwl:hasExactSynonym>
        <ns3:IAO_0000115>3M syndrome is a primordial growth disorder characterized by low birth weight, reduced birth length, severe postnatal growth restriction, a spectrum of minor anomalies (including facial dysmorphism) and normal intelligence.</ns3:IAO_0000115>
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