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        <rdfs:label>has symptom</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/DOID_3342 -->

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        <rdfs:label xml:lang="en">bone inflammation disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/DOID_4257 -->

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        <rdfs:label xml:lang="en">Caffey disease</rdfs:label>
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        <oboInOwl:hasDbXref>ICD10CM:M89.8</oboInOwl:hasDbXref>
        <oboInOwl:id>DOID:4257</oboInOwl:id>
        <ns4:IAO_0000115 xml:lang="en">A bone inflammation disease that causes bone changes, soft tissue swelling and irritability in infants. The disease has been associated with COL1A1 gene. It has symptom soft-tissue swelling, has symptom bone lesions, and has symptom irritability.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>MESH:D006958</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SNOMEDCT_US_2025_09_01:24752008</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MIM:114000</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS_CUI:C0020497</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCI:C84645</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:1051</oboInOwl:hasDbXref>
        <rdfs:comment xml:lang="en">OMIM mapping confirmed by DO. [SN].</rdfs:comment>
        <oboInOwl:hasExactSynonym xml:lang="en">cortical congenital hyperostosis</oboInOwl:hasExactSynonym>
        <oboInOwl:hasOBONamespace>disease_ontology</oboInOwl:hasOBONamespace>
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