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    <!-- http://purl.obolibrary.org/obo/MONDO_0006025 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0006025">
        <rdfs:label>autosomal recessive disease</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0011382 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0011382">
        <rdfs:label>sickle cell disease</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0006025"/>
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        <oboInOwl:hasDbXref>Orphanet:232</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MedDRA:10040641</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Sickle Cell Disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>NCIT:C34383</oboInOwl:hasDbXref>
        <ns2:IAO_0000115>Sickle cell anemias are chronic hemolytic diseases that may induce three types of acute accidents: severe anemia, severe bacterial infections, and ischemic vasoocclusive accidents (VOA) caused by sickle-shaped red blood cells obstructing small blood vessels and capillaries. Many diverse complications can occur.</ns2:IAO_0000115>
        <oboInOwl:hasExactSynonym>sickling disorder due to Hemoglobin S</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Hb-S/Hb-C disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MESH:D000755</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:282.60</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:0081445</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:282.63</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:287</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:2200624</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD10CM:D57.2</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:10923</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:603903</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>sickle cell disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>sickling disorder due to Haemoglobin S</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Haemoglobin S disease without crisis</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C0002895</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0008614</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>sickle cell anemia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>sickle-cell/Hb-C disease without crisis</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>NORD:1714</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:282.6</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019050 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019050">
        <rdfs:label>inherited hemoglobinopathy</rdfs:label>
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