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    <!-- http://purl.obolibrary.org/obo/MONDO_0009367 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0009367">
        <rdfs:label>McKusick-Kaufman syndrome</rdfs:label>
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        <oboInOwl:hasRelatedSynonym>HMCS</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>Kaufman-Mckusick syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>McKusick-Kaufman syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:id>MONDO:0009367</oboInOwl:id>
        <oboInOwl:hasRelatedSynonym>MKKS</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>OMIM:236700</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:184924</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>McKusick-Kaufman syndrome is a very rare, genetic developmental disorder presenting in the neonatal period characterized by genitourinary malformations, polydactyly, and more rarely, congenital heart disease or gastrointestinal malformations.</ns3:IAO_0000115>
        <oboInOwl:hasDbXref>Orphanet:2473</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>McKusick Kaufman syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>MESH:C538159</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0948368</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:702407009</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MedDRA:10052312</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>Kaufman McKusick syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>hydrometrocolpos-postaxial polydactyly syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICD9:758.89</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0003427</oboInOwl:hasDbXref>
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        <rdfs:label>multiple congenital anomalies/dysmorphic syndrome without intellectual disability</rdfs:label>
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