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    <!-- http://purl.obolibrary.org/obo/MONDO_0002254 -->

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        <rdfs:label>syndromic disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0003664 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0003664">
        <rdfs:label>hemolytic anemia</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0010263 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0010263">
        <rdfs:label>Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome</rdfs:label>
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        <oboInOwl:hasDbXref>GARD:0016761</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>ATS-MR</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>AMME complex</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>AMME syndrome</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>SCTID:720982007</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>DOID:0111860</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C564570</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>MEDGEN:337424</oboInOwl:hasDbXref>
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        <rdfs:label>multiple congenital anomalies/dysmorphic syndrome-intellectual disability</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0017007 -->

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        <rdfs:label>partial deletion of the long arm of chromosome X</rdfs:label>
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