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    <!-- http://purl.obolibrary.org/obo/MONDO_0000833 -->

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        <rdfs:label>bone remodeling disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0000845 -->

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        <oboInOwl:hasExactSynonym>fibrous dysplasia of bone</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICD9:733.29</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:10623005</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NORD:1147</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:120444</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>Orphanet:249</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C34609</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MedDRA:10016664</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0259779</oboInOwl:hasDbXref>
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        <ns5:IAO_0000115>A genetic, non-inheritable disorder caused by osteoblastic differentiation defects that result in the replacement of bone marrow and trabecular bone by fibrous stroma and immature bone. It usually affects a single bone and less frequently multiple bones. Skull, femur, tibia, and humerus are the most frequently affected bones. It manifests with pain, deformities, and fractures.</ns5:IAO_0000115>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019708 -->

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        <rdfs:label>obsolete primary bone dysplasia with disorganized development of skeletal components</rdfs:label>
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