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    <!-- http://purl.obolibrary.org/obo/MONDO_0008139 -->

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        <rdfs:label>OSLAM syndrome</rdfs:label>
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        <oboInOwl:hasDbXref>GARD:0004129</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>OSLAM syndrome</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>UMLS:C1833792</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>osteosarcoma, limb anomalies, and macrocytosis</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>osteosarcoma, limb anomalies (clinodactyly, absence of digital ray in foot, bilateral radioulnar synostosis) and macrocytosis without anaemia</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>OMIM:165660</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>osteosarcoma, limb anomalies (clinodactyly, absence of digital ray in foot, bilateral radioulnar synostosis) and macrocytosis without anemia</oboInOwl:hasRelatedSynonym>
        <ns3:IAO_0000115>OSLAM syndrome is characterized by the association of osteosarcoma, limb anomalies (clinodactyly with brachymesophalangy, bilateral radioulnar synostosis and absence of one digital ray of the foot) and red cell macrocytosis without anemia.</ns3:IAO_0000115>
        <oboInOwl:hasRelatedSynonym>osteosarcoma, limb anomalies, and erythroid macrocytosis with megaloblastic marrow</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>osteosarcoma-limb anomalies-erythroid macrocytosis syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:331588</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0008139</oboInOwl:id>
        <oboInOwl:hasDbXref>MESH:C537138</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:2760</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019054 -->

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