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    <!-- http://purl.obolibrary.org/obo/MONDO_0000226 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000226">
        <rdfs:label>mineral metabolism disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016761 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0016761">
        <rdfs:label>spondyloepiphyseal dysplasia</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019052 -->

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        <rdfs:label>inborn errors of metabolism</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019666 -->

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        <rdfs:label>spondyloepimetaphyseal dysplasia, PAPSS2 type</rdfs:label>
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        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/5280</ns4:IAO_0000233>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6752</ns4:IAO_0000233>
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        <ns4:IAO_0000115>A spondyloepimetaphyseal dysplasia characterized by short stature, short and bowed lower limbs, mild brachydactyly, kyphoscoliosis, abnormal gait, enlarged knee joints, precocious osteoarthropathy, and normal intelligence.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>GARD:0016813</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0019666</oboInOwl:id>
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        <oboInOwl:hasRelatedSynonym>BCYM4</oboInOwl:hasRelatedSynonym>
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        <oboInOwl:hasDbXref>Orphanet:93282</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>DOID:0050812</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C2748516</oboInOwl:hasDbXref>
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