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    <!-- http://purl.obolibrary.org/obo/MONDO_0000426 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000426">
        <rdfs:label>autosomal dominant disease</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0001576 -->

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        <rdfs:label>telangiectasis</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016231 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0016231">
        <rdfs:label>capillary malformation</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019180 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019180">
        <rdfs:label>hereditary hemorrhagic telangiectasia</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0000426"/>
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        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/5682</ns4:IAO_0000233>
        <ns2:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/hereditary_hemorrhagic_telangiectasia</ns2:curated_content_resource>
        <oboInOwl:hasDbXref>NANDO:1200744</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0019180</oboInOwl:id>
        <oboInOwl:hasDbXref>NCIT:C35064</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>icd11.foundation:714406192</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0006626</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIMPS:187300</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:2201034</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Rendu-Osler-Weber disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>Orphanet:774</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:2100296</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:448.0</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>A disorder of angiogenesis leading to arteriovenous dilatations: cutaneo-mucosal hemorrhagic telangiectasias and visceral shunting.</ns4:IAO_0000115>
        <oboInOwl:hasExactSynonym>hereditary hemorrhagic telangiectasia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C0039445</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NORD:1229</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>telangiectasia, hereditary Hemorrahagic, of Rendu, Osler</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Rendu-Osler disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>DOID:1270</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>telangiectasia, hereditary hemorrhagic</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>SCTID:21877004</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD10CM:I78.0</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Osler-Weber-Rendu disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MESH:D013683</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MedDRA:10019883</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:52657</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>HHT</oboInOwl:hasExactSynonym>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019293 -->

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        <rdfs:label>skin vascular disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019755 -->

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        <rdfs:label>developmental defect during embryogenesis</rdfs:label>
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