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    <!-- 
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_disorder"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#gard_rare"/>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_malformation_syndrome"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000233"/>
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    <!-- http://purl.obolibrary.org/obo/RO_0004003 -->

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        <rdf:type rdf:resource="http://www.w3.org/2002/07/owl#TransitiveProperty"/>
        <rdfs:label>has material basis in germline mutation in</rdfs:label>
    </ObjectProperty>
    


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    <!-- http://identifiers.org/hgnc/15979 -->

    <Class rdf:about="http://identifiers.org/hgnc/15979">
        <rdfs:label>TP63</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0011334 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0011334">
        <rdfs:label>limb-mammary syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0019287"/>
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                <someValuesFrom rdf:resource="http://identifiers.org/hgnc/15979"/>
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        </rdfs:subClassOf>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/4948</ns4:IAO_0000233>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6744</ns4:IAO_0000233>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6749</ns4:IAO_0000233>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6878</ns4:IAO_0000233>
        <ns5:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/limb_mammary_syndrome</ns5:curated_content_resource>
        <oboInOwl:hasDbXref>UMLS:C1863753</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:721972001</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:69085</oboInOwl:hasDbXref>
        <rdfs:comment>This term&#39;s classification was reviewed in the context of the Strategic Refinement project (2023) and was determined to be excluded from the &#39;disorder of visual system&#39; (MONDO:0024458) ontology branch (https://orcid.org/0000-0001-9310-0163)</rdfs:comment>
        <oboInOwl:hasDbXref>OMIM:603543</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>LMS</oboInOwl:hasExactSynonym>
        <oboInOwl:id>MONDO:0011334</oboInOwl:id>
        <oboInOwl:hasDbXref>MEDGEN:355051</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>Limb-mammary syndrome (LMS) is a rare disease belonging to the group of ectodermal dysplasias.</ns4:IAO_0000115>
        <oboInOwl:hasExactSynonym>limb-mammary syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>icd11.foundation:1958986288</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>mammary hypoplasia, ectrodactyly, and other hand/foot anomalies</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>GARD:0010051</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C535903</oboInOwl:hasDbXref>
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        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#ordo_malformation_syndrome"/>
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        <oboInOwl:inSubset rdf:resource="http://purl.obolibrary.org/obo/mondo#rare"/>
        <skos:exactMatch rdf:resource="http://www.orpha.net/ORDO/Orphanet_69085"/>
        <skos:exactMatch rdf:resource="https://omim.org/entry/603543"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019287 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019287">
        <rdfs:label>ectodermal dysplasia syndrome</rdfs:label>
    </Class>
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