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    <!-- http://purl.obolibrary.org/obo/MONDO_0001705 -->

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        <rdfs:label>pure red-cell aplasia</rdfs:label>
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        <oboInOwl:hasDbXref>NORD:1636</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:1340</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>A disease characterized by normocytic, normochromic anemia, low hematocrit, reticulocytopenia, and selective erythroid hypoplasia.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>GARD:0007504</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0034902</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Pure Red Cell Aplasia, Acquired</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>PRCA</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>NCIT:C34974</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:11154</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D012010</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:2100177</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:284.81</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0002280 -->

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    <!-- http://purl.obolibrary.org/obo/MONDO_0012197 -->

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