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    <!-- http://purl.obolibrary.org/obo/RO_0004029 -->

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        <rdfs:label>disease has feature</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/HP_0000668 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0000668">
        <rdfs:label>Hypodontia</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/HP_0001480 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0001480">
        <rdfs:label>Freckling</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/HP_0002164 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0002164">
        <rdfs:label>Nail dysplasia</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/HP_0003187 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0003187">
        <rdfs:label>Breast hypoplasia</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/HP_0008070 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0008070">
        <rdfs:label>Sparse hair</rdfs:label>
    </Class>
    


    <!-- 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_0007072 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0007072">
        <rdfs:label>ADULT syndrome</rdfs:label>
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        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0018234"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0019054"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0019287"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_1040001"/>
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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/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/adult_syndrome</ns5:curated_content_resource>
        <oboInOwl:hasDbXref>DOID:0050601</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0007072</oboInOwl:id>
        <oboInOwl:hasDbXref>MEDGEN:400232</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C1863204</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>acrodermatounguallacrimaltooth syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>ADULT syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>pigment anomaly-ectrodactyly-hypodontia syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>icd11.foundation:1445741645</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:103285</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0000384</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>ADULT (Acro-dermo-ungual-lacrimal-tooth) syndrome is a rare ectodermal dysplasia syndrome characterized by ectrodactyly, syndactyly, mammary hypoplasia, and excessive freckling as well as other typical ectodermal defects such as hypodontia, lacrimal duct anomalies, hypotrichosis, and onychodysplasia.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>MESH:C538052</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:720464003</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>acro-dermato-ungual-lacrimal-Tooth syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>acro-dermato-ungual-lacrimal-tooth syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>acro dermato ungual lacrimal tooth syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>Orphanet:978</oboInOwl:hasDbXref>
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        <skos:exactMatch rdf:resource="http://www.orpha.net/ORDO/Orphanet_978"/>
        <skos:exactMatch rdf:resource="https://omim.org/entry/103285"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0018234 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0018234">
        <rdfs:label>dysostosis</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0019054 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019054">
        <rdfs:label>congenital limb malformation</rdfs:label>
    </Class>
    


    <!-- 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>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_1040001 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_1040001">
        <rdfs:label>TP63-related ectodermal dysplasia spectrum with limb and orofacial malformations</rdfs:label>
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