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    <!-- http://purl.obolibrary.org/obo/MONDO_0007245 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0007245">
        <rdfs:label>cafe au lait spots, multiple</rdfs:label>
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        <oboInOwl:id>MONDO:0007245</oboInOwl:id>
        <oboInOwl:hasExactSynonym>familial café-au-lait spots</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>neurofibromatosis type 6</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasExactSynonym>multiple café-au-lait syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>autosomal dominant café au lait spots</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:114030</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:396266</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>multiple cafe-au-lait syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>cafe-au-lait spots, multiple</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>multiple cafe-au-lait spots</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0003967</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>A cutaneous disorder characterized by the presence of several cafe-au-lait (CAL) macules without any other manifestations of neurofibromatosis or any other systemic disorder.</ns3:IAO_0000115>
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