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        <rdfs:label>disease has feature</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/HP_0001373 -->

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        <rdfs:label>Joint dislocation</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0007875 -->

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        <rdfs:label>Larsen syndrome</rdfs:label>
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        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/6860/larsen-syndrome</rdfs:seeAlso>
        <ns3:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/larsen_syndrome</ns3:curated_content_resource>
        <oboInOwl:hasRelatedSynonym>LRS</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>OMIM:150250</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:2201019</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NORD:1349</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0007875</oboInOwl:id>
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        <oboInOwl:hasDbXref>icd11.foundation:607849551</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:759.89</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0175778</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>autosomal dominant Larsen syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>MEDGEN:104500</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:503</oboInOwl:hasDbXref>
        <ns5:IAO_0000115>A rare skeletal dysplasia characterized by congenital dislocation of large joints, foot deformities, cervical spine dysplasia, scoliosis, spatula-shaped distal phalanges and distinctive craniofacial abnormalities, including cleft palate.</ns5:IAO_0000115>
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        <oboInOwl:hasDbXref>DOID:14764</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0006860</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019700 -->

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        <rdfs:label>obsolete primary bone dysplasia with multiple joint dislocations</rdfs:label>
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        <rdfs:label>developmental defect during embryogenesis</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_1060173 -->

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        <rdfs:label>FLNB-associated autosomal dominant filamin related bone disorder</rdfs:label>
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