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

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        <rdfs:label>syndromic intellectual disability</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_0016433 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0016433">
        <rdfs:label>dysmorphism-short stature-deafness-disorder of sex development syndrome</rdfs:label>
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        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/5588</ns4:IAO_0000233>
        <ns2:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/dysmorphism_short_stature_deafness_difference_of_sex_development_syndrome</ns2:curated_content_resource>
        <oboInOwl:hasDbXref>UMLS:C4518561</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0016433</oboInOwl:id>
        <oboInOwl:hasExactSynonym>Dysmorphism-short stature-deafness-pseudohermaphroditism syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:1383129</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0018764</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>Dysmorphism-short stature-deafness-disorder of sex development syndrome is characterized by dysmorphism (including facial asymmetry, arched eyebrows, hypertelorism, broad and flat nasal bridge, microtia, small nose with anteverted nostrils, micrognathia), deafness, cleft palate, male pseudohermaphroditism, and growth and psychomotor retardation. It has been described in two siblings. It is transmitted as an autosomal recessive trait.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>Orphanet:2282</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0020040 -->

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        <rdfs:label>46,XY disorder of sex development</rdfs:label>
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