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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- http://purl.obolibrary.org/obo/HP_0002666 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0002666">
        <rdfs:label>Pheochromocytoma</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/HP_0100634"/>
        <oboInOwl:id>HP:0002666</oboInOwl:id>
        <oboInOwl:hasDbXref>SNOMEDCT_US:302835009</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>Pheochromocytomas (also known as chromaffin tumors) produce, store, and secrete catecholamines. Pheochromocytomas usually originate from the adrenal medulla but may also develop from chromaffin cells in or about sympathetic ganglia. A common symptom of pheochromocytoma is hypertension owing to release of catecholamines.</ns3:IAO_0000115>
        <oboInOwl:hasExactSynonym>Chromaffin tumors</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C0031511</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Chromaffin tumours</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>SNOMEDCT_US:399343007</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C3326</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SNOMEDCT_US:85583005</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/HP_0100634 -->

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        <rdfs:label>Neuroendocrine neoplasm</rdfs:label>
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