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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/mondo#ordo_malformation_syndrome"/>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0003847 -->

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        <rdfs:label>hereditary disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0007584 -->

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        <rdfs:label>exostoses-anetodermia-brachydactyly type E syndrome</rdfs:label>
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        <ns4:IAO_0000115>Exostoses-anetodermia-brachydactyly type E syndrome is an association reported in a single kindred characterized by the variable presence of the following features: anetodermia (macular atrophy of the skin), multiple exostoses, and brachydactyly type E. There have been no further descriptions in the literature since 1985.</ns4:IAO_0000115>
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        <oboInOwl:hasDbXref>OMIM:133690</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C565034</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0007584</oboInOwl:id>
        <oboInOwl:hasDbXref>GARD:0002202</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:1962</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019708 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0019708">
        <rdfs:label>obsolete primary bone dysplasia with disorganized development of skeletal components</rdfs:label>
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