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    <!-- http://purl.obolibrary.org/obo/MONDO_0003847 -->

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        <rdfs:label>hereditary disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0005509 -->

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        <rdfs:label>histiocytoma</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0012809 -->

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        <rdfs:label>histiocytoma, Angiomatoid fibrous</rdfs:label>
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        <oboInOwl:hasExactSynonym>histiocytoma, angiomatoid fibrous, somatic</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>AFH</oboInOwl:hasExactSynonym>
        <oboInOwl:id>MONDO:0012809</oboInOwl:id>
        <oboInOwl:hasDbXref>OMIM:612160</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>angiomatoid fibrous histiocytoma</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0022303</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:569164</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>A low malignant potential soft tissue neoplasm of uncertain differentiation. It typically affects young patients, presenting as a slowly growing nodular or cystic tumor mass, most often in the subcutaneous tissues of the extremities. Occasionally, patients have systemic symptoms (anemia, fever, and weight loss). This tumor has a relatively good prognosis. A minority of patients develop local recurrences. Metastases are rare.</ns3:IAO_0000115>
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