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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_0018569 -->

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        <rdfs:label>X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome</rdfs:label>
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        <oboInOwl:hasDbXref>UMLS:C5681178</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:1812501</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome is a rare syndromic intellectual disability characterized by hypotonia, microcephaly, severe developmental delay, seizures, intellectual disability, growth retardation, cardiovascular septal defects, cryptorchidism, hypospadias, and dysmorphic features - prominent ears, prognathism, thin upper lip, dental crowding.</ns4:IAO_0000115>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0020119 -->

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