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    <!-- http://purl.obolibrary.org/obo/MONDO_0019906 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019906">
        <rdfs:label>ring chromosome 11</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0700018"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0700091"/>
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        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/ring_chromosome_11</ns4:curated_content_resource>
        <oboInOwl:hasDbXref>Orphanet:96175</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0010846</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>chromosome 11 ring</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>r(11) syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>Ring 11</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>r11</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>ICD9:758.89</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>RC11</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:539256</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>Ring chromosome 11 syndrome is an autosomal anomaly characterized by variable clinical features, including early growth retardation and short stature, microcephaly, developmental delay, some degree of intellectual disability, facial dysmorphism and café-au-lait spots. In some cases, congenital heart disease and endocrine abnormalities have been reported.</ns3:IAO_0000115>
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        <oboInOwl:hasDbXref>UMLS:C0265444</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Ring chromosome type 11</oboInOwl:hasExactSynonym>
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        <rdfs:label>ring chromosome disorder</rdfs:label>
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    <!-- http://www.orpha.net/ORDO/Orphanet_96175 -->

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        <rdfs:label>obsolete_ring chromosome 11</rdfs:label>
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