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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_disorder"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#curated_content_resource"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000231"/>
    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#hasDbXref"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000233"/>
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    <AnnotationProperty rdf:about="http://www.geneontology.org/formats/oboInOwl#id"/>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_morphological_anomaly"/>
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    <!-- http://purl.obolibrary.org/obo/HP_0009743 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0009743">
        <rdfs:label>Distichiasis</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0007464 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0007464">
        <rdfs:label>obsolete isolated distichiasis</rdfs:label>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/1501</ns4:IAO_0000233>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/7693</ns4:IAO_0000233>
        <ns5:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/distichiasis</ns5:curated_content_resource>
        <deprecated rdf:datatype="http://www.w3.org/2001/XMLSchema#boolean">true</deprecated>
        <oboInOwl:hasDbXref>OMIM:126300</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0007464</oboInOwl:id>
        <ns4:IAO_0000115>OBSOLETE. Isolated distichiasis is a rare congenital eyelid anomaly characterized by an accessory row of eyelashes (that may be partial or complete) posterior to the normal row of cilia, at or close to the meibomian gland orifices, that is not associated with any other condition, and that may lead to ocular irritation and corneal damage if left untreated.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>SCTID:95339000</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:743.63</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:99177</oboInOwl:hasDbXref>
        <rdfs:comment>Reason of obsoletion: is a phenotype and not a disease - MONDO:excludePhenotype. Term to consider: HP:0009743</rdfs:comment>
        <skos:exactMatch rdf:resource="http://identifiers.org/snomedct/95339000"/>
        <oboInOwl:consider rdf:resource="http://purl.obolibrary.org/obo/HP_0009743"/>
        <ns4:IAO_0000231 rdf:resource="http://purl.obolibrary.org/obo/OMO_0001000"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#ordo_disorder"/>
        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#ordo_morphological_anomaly"/>
        <skos:exactMatch rdf:resource="http://www.orpha.net/ORDO/Orphanet_99177"/>
        <skos:exactMatch rdf:resource="https://omim.org/entry/126300"/>
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