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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>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0008894 -->

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        <rdfs:label>cataract-hypertrichosis-intellectual disability 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/cahmr_syndrome</ns2:curated_content_resource>
        <oboInOwl:id>MONDO:0008894</oboInOwl:id>
        <oboInOwl:hasExactSynonym>CAHMR syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0001052</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:722379001</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>Cataract-hypertrichosis-intellectual disability syndrome is characterized by congenital cataract, generalized hypertrichosis and intellectual deficit. It has been described in two Egyptian sibs born to consanguineous parents. It is transmitted as an autosomal recessive trait.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>MESH:C537959</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>cataract, hypertrichosis, mental retardation syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>Orphanet:1375</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:167117</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0796282</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:211770</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019280 -->

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        <rdfs:label>hypertrichosis</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019287 -->

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        <rdfs:label>ectodermal dysplasia syndrome</rdfs:label>
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