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    <!-- http://purl.obolibrary.org/obo/MONDO_0000508 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000508">
        <rdfs:label>syndromic intellectual disability</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0002254 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0002254">
        <rdfs:label>syndromic disease</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0009318 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0009318">
        <rdfs:label>Hallermann-Streiff syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0800063"/>
        <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/6227</ns4:IAO_0000233>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/288/hallermann-streiff-syndrome</rdfs:seeAlso>
        <ns2:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/hallermann_streiff_syndrome</ns2:curated_content_resource>
        <oboInOwl:hasRelatedSynonym>HSS</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>NANDO:2200973</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:234100</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C84746</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0009318</oboInOwl:id>
        <oboInOwl:hasRelatedSynonym>Hallermann Streiff Francois syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>MEDGEN:5414</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>oculomandibulofacial syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>Hallermann Streiff syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>Francois dyscephalic syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>Orphanet:2108</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0018522</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:4534</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Hallermann&#39;s syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MESH:D006210</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>François dyscephalic syndrome</oboInOwl:hasExactSynonym>
        <ns4:IAO_0000115>Hallermann-Streiff syndrome is a rare genetic syndrome characterized mainly by head and facial abnormalities such as bird-like facies (with beak-shaped nose and retrognathia), hypoplastic mandible, brachycephaly with frontal bossing, dental abnormalities (e.g. absence of teeth, natal teeth, supernumerary teeth, severe agenesis of permanent teeth, enamel hypoplasia) hypotrichosis, various ophthalmic disorders (e.g. congenital cataracts, bilateral microphthalmia, ptosis, nystagmus) and atrophy of skin (especially around the center of face and nose) as well as telangiectasia and proportionate short stature. Intellectual disability is reported in some cases.</ns4:IAO_0000115>
        <oboInOwl:hasExactSynonym>Hallermann syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>SCTID:7903009</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0000288</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NORD:1888</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>FranC&#39;ois dyscephalic syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Hallermann-Streiff syndrome</oboInOwl:hasExactSynonym>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015160 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015160">
        <rdfs:label>multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0015329 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015329">
        <rdfs:label>obsolete malformation syndrome with short stature</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_0019303 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019303">
        <rdfs:label>premature aging syndrome</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0019699 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019699">
        <rdfs:label>obsolete slender bone dysplasia</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0020188 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020188">
        <rdfs:label>obsolete congenital absence of the eyebrow/eyelashes</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0020234 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020234">
        <rdfs:label>obsolete craniofacial anomaly with cataract</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0043007 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0043007">
        <rdfs:label>obsolete genetic multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0800063 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0800063">
        <rdfs:label>primordial dwarfism and slender bone disorder</rdfs:label>
    </Class>
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