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    <!-- http://purl.obolibrary.org/obo/MONDO_0009121 -->

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        <rdfs:label>von Voss-Cherstvoy syndrome</rdfs:label>
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        <oboInOwl:hasDbXref>Orphanet:3439</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>phocomelia thrombocytopenia encephalocele and urogenital malformations</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>SCTID:719021005</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>UMLS:C1857226</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0001894</oboInOwl:hasDbXref>
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        <oboInOwl:hasRelatedSynonym>Von Voss Cherstvoy syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>von Voss-Cherstvoy syndrome</oboInOwl:hasExactSynonym>
        <ns3:IAO_0000115>Von Voss-Cherstvoy syndrome is a very rare disorder with phocomelia of upper limbs, encephalocele, variable brain anomalies, urogenital abnormalities, and thrombocytopenia.</ns3:IAO_0000115>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015161 -->

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        <rdfs:label>multiple congenital anomalies/dysmorphic syndrome without intellectual disability</rdfs:label>
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