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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_0007872 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0007872">
        <rdfs:label>LADD syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0000426"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0015161"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0800066"/>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/4948</ns4:IAO_0000233>
        <ns2:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/lacrimoauriculodentodigital_syndrome_1</ns2:curated_content_resource>
        <oboInOwl:hasExactSynonym>LACRIMOAURICULODENTODIGITAL syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>DOID:0050331</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:2363</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:759.89</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:0081370</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0007872</oboInOwl:id>
        <oboInOwl:hasExactSynonym>Lacrimoauriculoradiodental syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0006848</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:23817003</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NORD:1345</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>lard syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>LADD</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>Lacrimoauriculodento-digital syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MESH:C538132</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:78545</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>A multiple congenital anomaly syndrome characterized by hypoplasia, aplasia or atresia of the lacrimal system; anomalies of the ears and hearing loss; hypoplasias, apalsias or atresias of the salivary glands; dental anomalies and digital malformations.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>UMLS:C0265269</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Levy Hollister syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>LADD syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Levy-Hollister syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>lacrimoauriculodentodigital syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIMPS:149730</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Lacrimo-auriculo-dento-digital syndrome</oboInOwl:hasExactSynonym>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015161 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015161">
        <rdfs:label>multiple congenital anomalies/dysmorphic syndrome without intellectual disability</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015503 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015503">
        <rdfs:label>obsolete nose and cavum anomaly</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0018562 -->

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        <rdfs:label>obsolete hereditary otorhinolaryngological malformation</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0020197 -->

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        <rdfs:label>obsolete EEC syndrome and related syndrome</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0800066 -->

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        <rdfs:label>polydactyly-syndactyly-triphalangism</rdfs:label>
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