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

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        <rdfs:label>syndromic disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015159 -->

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        <rdfs:label>multiple congenital anomalies/dysmorphic syndrome-intellectual disability</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019414 -->

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        <rdfs:label>BRESEK syndrome</rdfs:label>
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        <ns2:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/bresek_syndrome</ns2:curated_content_resource>
        <oboInOwl:hasDbXref>UMLS:C3502469</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>A syndrome characterized by Brain anomalies, severe mental Retardation, Ectodermal dysplasia, Skeletal deformities (vertebral anomalies, scoliosis, polydactyly), Ear/eye anomalies (maldevelopment, small optic nerves, low set and large ears with hearing loss) and Kidney dysplasia/hypoplasia (giving the acronym BRESEK syndrome).</ns4:IAO_0000115>
        <oboInOwl:hasExactSynonym>BRESHECK syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0016746</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C564519</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:502868</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:717945001</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0019414</oboInOwl:id>
        <oboInOwl:hasDbXref>Orphanet:85284</oboInOwl:hasDbXref>
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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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    <!-- http://purl.obolibrary.org/obo/MONDO_0100213 -->

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        <rdfs:label>IFAP syndrome 1, with or without BRESHECK syndrome</rdfs:label>
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