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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000233"/>
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    <!-- http://purl.obolibrary.org/obo/RO_0004029 -->

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        <rdfs:label>disease has feature</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/HP_0004348 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0004348">
        <rdfs:label>Abnormality of bone mineral density</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0011976 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0011976">
        <rdfs:label>lipodystrophy-intellectual disability-deafness syndrome</rdfs:label>
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        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/1567</ns5:IAO_0000233>
        <ns3:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/lipodystrophy_generalized_with_impaired_intellectual_development_deafness_short_stature_and_slender_bones</ns3:curated_content_resource>
        <ns3:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/lipodystrophy_intellectual_disability_deafness_syndrome</ns3:curated_content_resource>
        <oboInOwl:hasDbXref>GARD:0016646</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:721973006</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0011976</oboInOwl:id>
        <oboInOwl:hasDbXref>UMLS:C1842465</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C564283</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>lipodystrophy, generalized, with intellectual disability, deafness, short stature, and slender bones</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>Orphanet:50811</oboInOwl:hasDbXref>
        <ns5:IAO_0000115>Lipodystrophy-intellectual disability-deafness syndrome is an extremely rare form of genetic lipodystrophy, reported in 3 patients from one family to date, characterized by generalized congenital lipodystrophy, low birth weight, progressive sensorineural deafness occurring in childhood, intellectual deficit, progressive osteopenia, delayed skeletal maturation, skeletal abnormalities described as slender, undermineralized tubular bones, and dense metaphyseal striations in the distal femur, ulna and radius of older patients. Autosomal recessive inheritance has been suggested.</ns5:IAO_0000115>
        <oboInOwl:hasDbXref>MEDGEN:334166</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Rajab-Spranger syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:608154</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>lipodystrophy, generalized, with mental retardation, deafness, short stature, and slender bones</oboInOwl:hasRelatedSynonym>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015333 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0015333">
        <rdfs:label>progeroid syndrome</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MONDO_0019705 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019705">
        <rdfs:label>obsolete primary bone dysplasia with defective bone mineralization</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0020087 -->

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        <rdfs:label>hereditary lipodystrophy</rdfs:label>
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