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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#otar"/>
    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_malformation_syndrome"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0009856 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0009856">
        <rdfs:label>Peters plus syndrome</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0017770 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0017770">
        <rdfs:label>obsolete Robinow-like syndrome</rdfs:label>
        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/9206</ns4:IAO_0000233>
        <deprecated rdf:datatype="http://www.w3.org/2001/XMLSchema#boolean">true</deprecated>
        <ns4:IAO_0000115>OBSOLETE. Robinow-like syndrome is characterized by the association of the clinical features present in Robinow syndrome (short stature, mesomelic brachymelia, macrocephaly, and hypoplastic genitalia), with anterior chamber cleavage anomalies. It has been described in two sisters and is transmitted as an autosomal recessive trait.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>SCTID:721905000</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0017770</oboInOwl:id>
        <oboInOwl:hasDbXref>Orphanet:3105</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Saal-Greenstein syndrome</oboInOwl:hasExactSynonym>
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