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    <!-- http://purl.obolibrary.org/obo/MONDO_0019027 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019027">
        <rdfs:label>otopalatodigital syndrome</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0020119 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0020119">
        <rdfs:label>X-linked syndromic intellectual disability</rdfs:label>
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        <rdfs:label>Syndromic developmental defect of the eye</rdfs:label>
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    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_2484">
        <rdfs:label>Osteodysplasty, Melnick-Needles type</rdfs:label>
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        <oboInOwl:hasDbXref>UMLS:C0025237</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD10:Q77.8</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>Osteodysplasty, Melnick-Needles type (MNS) is a severe form of frontootopalatodigital syndrome (see this term) and is associated with a short stature, facial dysmorphism, osseous abnormalities involving the majority of the axial and appendicular skeleton resulting in significant effects on the craniofacial skeleton including impaired speech and masticatory problems.</ns3:IAO_0000115>
        <oboInOwl:hasExactSynonym>Melnick-Needles syndrome</oboInOwl:hasExactSynonym>
        <ns4:definition_citation>orphanet</ns4:definition_citation>
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    <!-- http://www.orpha.net/ORDO/Orphanet_98638 -->

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        <rdfs:label>Rare disease with glaucoma as a major feature</rdfs:label>
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