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    <!-- http://purl.obolibrary.org/obo/DOID_14793 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/DOID_14793">
        <rdfs:label>hypohidrotic ectodermal dysplasia</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/DOID_2121"/>
        <oboInOwl:hasExactSynonym xml:lang="en">Christ-Siemens-Touraine Syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasOBONamespace>disease_ontology</oboInOwl:hasOBONamespace>
        <oboInOwl:hasDbXref>GARD:76</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ORDO:238468</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D053358</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>NCI:C84562</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:224900</oboInOwl:hasDbXref>
        <ns2:IAO_0000115>An ectodermal dysplasia that is characterized by malformation of ectodermal (skin, hair, teeth and sweat glands) structures including hypotrichosis (sparseness of scalp and body hair), hypohidrosis (reduced ability to sweat), and hypodontia (congenital absence of teeth).</ns2:IAO_0000115>
        <oboInOwl:hasDbXref>UMLS_CUI:C0162359</oboInOwl:hasDbXref>
        <oboInOwl:id>DOID:14793</oboInOwl:id>
        <oboInOwl:hasDbXref>OMIM:129490</oboInOwl:hasDbXref>
        <oboInOwl:hasAlternativeId>DOID:0050447</oboInOwl:hasAlternativeId>
        <oboInOwl:hasDbXref>OMIM:300291</oboInOwl:hasDbXref>
        <oboInOwl:hasAlternativeId>DOID:0050446</oboInOwl:hasAlternativeId>
        <oboInOwl:hasExactSynonym xml:lang="en">Ectodermal Dysplasia 1, Anhydrotic</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym xml:lang="en">Hypohidrotic X-linked ectodermal dysplasia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:305100</oboInOwl:hasDbXref>
        <rdfs:comment>OMIM mapping confirmed by DO. [SN].</rdfs:comment>
        <oboInOwl:hasExactSynonym xml:lang="en">anhidrotic ectodermal dysplasia 3</oboInOwl:hasExactSynonym>
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        <rdfs:label>ectodermal dysplasia</rdfs:label>
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