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    <!-- http://purl.obolibrary.org/obo/DOID_0050120 -->

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        <rdfs:label>hemophagocytic syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/DOID_225"/>
        <rdfs:comment>&quot;A syndrome that is characterized by an expansion of the monocyte-macrophage population and intense hemophagocytosis. It can occur de novo, but more often occurs in the setting of another disorder, usually an infection or a malignancy. A clinical picture of fever, hepatosplenomegaly, lymphadenopathy and peripheral pancytopenia. The morphologic hallmark of this syndrome is the phagocytosis of hematopoietic elements by morphologically normal macrophages.&quot; [url:http\://www.mayoclinicproceedings.com/inside.asp?AID=57&amp;UID=, url:http\://www.scielo.br/scielo.php?script=sci_arttext&amp;pid=S1516-31801997000500007&amp;lng=pt&amp;nrm=iso]</rdfs:comment>
        <rdfs:seeAlso>URI: http://www.ebi.ac.uk/cellline#hemophagocytic_syndrome</rdfs:seeAlso>
        <ns2:IAO_0000118>&quot;haemophagocytic syndrome&quot; EXACT []</ns2:IAO_0000118>
        <ns2:IAO_0000118>&quot;HPS&quot; EXACT []</ns2:IAO_0000118>
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        <rdfs:label>syndrome</rdfs:label>
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