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     xmlns:oboInOwl="http://www.geneontology.org/formats/oboInOwl#"
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000412"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasBroadSynonym"/>
    


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    <!-- 
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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>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_7770009"/>
        <rdfs:comment>Usage note: this is intended only for diseases with an inherited genetic etiology. Somatic genetic mutations are excluded. Some ontologies use the term &#39;genetic disease&#39; in the sense of inherited disorders only, we are here careful to distinguish.</rdfs:comment>
        <oboInOwl:hasExactSynonym>hereditary disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>NCIT:C3101</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0019247</oboInOwl:hasDbXref>
        <oboInOwl:hasBroadSynonym>genetic condition</oboInOwl:hasBroadSynonym>
        <oboInOwl:hasDbXref>DOID:630</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>inherited genetic disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:5527</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:799.89</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>hereditary disease or disorder</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>molecular disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>hereditary diseases</oboInOwl:hasExactSynonym>
        <oboInOwl:hasBroadSynonym>genetic disorder</oboInOwl:hasBroadSynonym>
        <ns2:IAO_0000115>A disease that is caused by genetic modifications where those modifications are inherited from a parent&#39;s genome.</ns2:IAO_0000115>
        <oboInOwl:hasDbXref>EFO:0000508</oboInOwl:hasDbXref>
        <oboInOwl:hasBroadSynonym>genetic disease</oboInOwl:hasBroadSynonym>
        <oboInOwl:hasDbXref>SCTID:32895009</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D030342</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>inherited disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasNarrowSynonym>Mendelian disease</oboInOwl:hasNarrowSynonym>
        <oboInOwl:inSubset rdf:resource="http://purl.oboInOwllibrary.org/oboInOwl/mondo#harrisons_view"/>
        <oboInOwl:inSubset rdf:resource="http://purl.oboInOwllibrary.org/oboInOwl/mondo#otar"/>
        <oboInOwl:inSubset rdf:resource="http://purl.oboInOwllibrary.org/oboInOwl/mondo#rare_grouping"/>
        <ns2:IAO_0000412 rdf:resource="http://purl.obolibrary.org/obo/mondo.owl"/>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_7770009 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_7770009">
        <rdfs:label>disease of genetic or genomic mechanism</rdfs:label>
    </Class>
</rdf:RDF>



<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



