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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_0002254 -->

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        <rdfs:label>syndromic disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0011640 -->

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        <rdfs:label>genitopatellar syndrome</rdfs:label>
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        <oboInOwl:hasDbXref>MEDGEN:381208</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0011640</oboInOwl:id>
        <oboInOwl:hasExactSynonym>genitopatellar syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MESH:C565255</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>absent patellae, scrotal hypoplasia, renal anomalies, Facial Dysmorphism, and mental retardation</oboInOwl:hasRelatedSynonym>
        <ns4:IAO_0000115>Genitopatellar syndrome is a rare congenital patellar anomaly syndrome characterized by patellar aplasia or hypoplasia associated with microcephaly, characteristic coarse facial features (microcephaly, bitemporal narrowing, large, broad nose with high nasal bridge, prominent cheeks and micro/retrognathia or prognathism), arthrogryposis of the hips and knees, urogenital abnormalities and intellectual deficiency.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>OMIM:606170</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:759.89</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>absent patellae-scrotal hypoplasia-renal anomalies-facial dysmorphism-intellectual disability syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0010994</oboInOwl:hasDbXref>
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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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        <rdfs:label>skeletal dysplasia</rdfs:label>
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