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    <!-- http://purl.obolibrary.org/obo/MONDO_0010111 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0010111">
        <rdfs:label>odontotrichomelic syndrome</rdfs:label>
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        <oboInOwl:hasExactSynonym>Freire-Maia odontotrichomelic syndrome</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>SCTID:239028001</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>Odontotrichomelic syndrome is characterized by malformations of all four extremities, hypoplastic nails, ear anomalies, hypotrichosis, abnormal dentition, hyperhidrosis and nasolacrimal duct obstruction. So far, it has been described in less than 10 patients. Transmission is autosomal recessive.</ns3:IAO_0000115>
        <oboInOwl:hasExactSynonym>odontotrichomelic hypohidrotic dysplasia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>odontotrichomelic syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:443944</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0002381</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Freire-Maia syndrome</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>OMIM:273400</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0010111</oboInOwl:id>
        <oboInOwl:hasExactSynonym>tetramelic deficiencies, ectodermal dysplasia, deformed ears, and other abnormalities</oboInOwl:hasExactSynonym>
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        <rdfs:label>ectodermal dysplasia syndrome</rdfs:label>
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