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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_0100306 -->

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        <rdfs:label>Muscle fiber hyaline bodies</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0000727 -->

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        <rdfs:label>scapuloperoneal myopathy</rdfs:label>
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        <rdfs:label>X-linked scapuloperoneal muscular dystrophy</rdfs:label>
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        <ns5:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/x_linked_scapuloperoneal_muscular_dystrophy</ns5:curated_content_resource>
        <oboInOwl:hasDbXref>UMLS:C2678061</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>scapuloperoneal myopathy, X-linked dominant, X-linked dominant</oboInOwl:hasExactSynonym>
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        <ns4:IAO_0000115>X-linked scapuloperoneal muscular dystrophy (X-linked SPMD) is a skeletal muscle disease characterized by late onset, co-occurrence of scapular and peroneal muscle weakness, and scapular winging.</ns4:IAO_0000115>
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        <oboInOwl:hasDbXref>Orphanet:431272</oboInOwl:hasDbXref>
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        <rdfs:label>FHL1-related myopathy</rdfs:label>
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