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    <!-- http://www.orpha.net/ORDO/Orphanet_124 -->

    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_124">
        <rdfs:label>Blackfan-Diamond anemia</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://www.orpha.net/ORDO/Orphanet_156237"/>
        <rdfs:subClassOf rdf:resource="http://www.orpha.net/ORDO/Orphanet_183422"/>
        <rdfs:subClassOf rdf:resource="http://www.orpha.net/ORDO/Orphanet_68383"/>
        <rdfs:subClassOf rdf:resource="http://www.orpha.net/ORDO/Orphanet_79191"/>
        <oboInOwl:hasExactSynonym>Congenital hypoplastic anemia, Blackfan-Diamond type</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:612562</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:612561</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:612563</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:606129</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:614900</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:612528</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:612527</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD10:D61.0</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Congenital PRCA</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:606164</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:615909</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:105650</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Aase-Smith II syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:617911</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C1260899</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Aase syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:615550</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:618310</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Congenital pure red cell aplasia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:613309</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:613308</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MedDRA:10062989</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:610629</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:617409</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:617408</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D029503</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:618312</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:618313</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:300946</oboInOwl:hasDbXref>
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    <!-- http://www.orpha.net/ORDO/Orphanet_156237 -->

    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_156237">
        <rdfs:label>Syndrome or malformation associated with head and neck malformations</rdfs:label>
    </Class>
    


    <!-- http://www.orpha.net/ORDO/Orphanet_183422 -->

    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_183422">
        <rdfs:label>Polymalformative genetic syndrome with increased risk of developing cancer</rdfs:label>
    </Class>
    


    <!-- http://www.orpha.net/ORDO/Orphanet_68383 -->

    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_68383">
        <rdfs:label>Rare constitutional medullar aplasia</rdfs:label>
    </Class>
    


    <!-- http://www.orpha.net/ORDO/Orphanet_79191 -->

    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_79191">
        <rdfs:label>Disorder of purine metabolism</rdfs:label>
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