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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_0010749 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0010749">
        <rdfs:label>trigonocephaly-short stature-developmental delay syndrome</rdfs:label>
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        <oboInOwl:hasDbXref>MESH:C536620</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Say-Meyer syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>trigonocephaly with short stature and developmental delay</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>SCTID:733066002</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>A syndrome characterized by short stature, trigonocephaly and developmental delay. It has been described in three males. Moderate intellectual deficit was reported in one of the males and the other two patients displayed psychomotor retardation. X-linked transmission has been suggested but autosomal recessive inheritance can not be ruled out.</ns4:IAO_0000115>
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        <oboInOwl:hasRelatedSynonym>Say Meyer syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>GARD:0000243</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0010749</oboInOwl:id>
        <oboInOwl:hasDbXref>OMIM:314320</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C1839125</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:3369</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:374138</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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    <!-- http://purl.obolibrary.org/obo/MONDO_0015338 -->

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        <rdfs:label>syndromic craniosynostosis</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0020119 -->

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