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

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0003847">
        <rdfs:label>hereditary disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019040 -->

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        <rdfs:label>chromosomal disorder</rdfs:label>
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        <oboInOwl:hasRelatedSynonym>chromosome disorder, autosomal</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>chromosome abnormality disorder</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>chromosomal disorder</oboInOwl:hasExactSynonym>
        <oboInOwl:id>MONDO:0019040</oboInOwl:id>
        <oboInOwl:hasDbXref>MEDGEN:3441</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>chromosome disorder</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>DOID:0080014</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C34470</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>autosomal chromosome disorder</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>SCTID:409709004</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:68335</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:2100280</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>disorders, chromosome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>disorder, chromosome abnormality</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>ICD10CM:Q90-Q99</oboInOwl:hasDbXref>
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        <oboInOwl:hasExactSynonym>disorders, chromosomal</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>NANDO:1100014</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D025063</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>autosomal chromosome disorders</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>ICD9:758.89</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>Clinical conditions caused by an abnormal chromosome constitution in which there is extra or missing chromosome material (either a whole chromosome or a chromosome segment). (from Thompson et al., Genetics in Medicine, 5th ed, p429)</ns4:IAO_0000115>
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        <oboInOwl:hasDbXref>NANDO:2100279</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0008626</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019755 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019755">
        <rdfs:label>developmental defect during embryogenesis</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_7770009 -->

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