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    <!-- http://www.ebi.ac.uk/efo/EFO_0000463 -->

    <Class rdf:about="http://www.ebi.ac.uk/efo/EFO_0000463">
        <rdfs:label>Emery-Dreifuss muscular dystrophy</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://www.ebi.ac.uk/efo/EFO_0000757"/>
        <ns2:IAO_0000119>DOID:11726</ns2:IAO_0000119>
        <ns2:IAO_0000117>James Malone</ns2:IAO_0000117>
        <ns2:IAO_0000118>Emery-Dreifuss muscular dystrophy (disorder)</ns2:IAO_0000118>
        <ns2:IAO_0000118>EMD - Emery-Dreifuss muscular dystrophy</ns2:IAO_0000118>
        <ns2:IAO_0000118>Hauptmann-Thannhauser Muscular Dystrophy</ns2:IAO_0000118>
        <ns2:IAO_0000118>Muscular Dystrophy, Scapuloperoneal</ns2:IAO_0000118>
        <ns2:IAO_0000119>SNOMEDCT:111508004</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:12467752</ns2:IAO_0000119>
        <ns2:IAO_0000118>Emery-Dreifuss Muscular Dystrophy 2</ns2:IAO_0000118>
        <ns2:IAO_0000118>Emery Dreifuss Syndrome</ns2:IAO_0000118>
        <rdfs:seeAlso>URI: http://www.ebi.ac.uk/cellline#Emery-Dreifuss_muscular_dystrophy</rdfs:seeAlso>
        <ns2:IAO_0000119>MSH:D020389</ns2:IAO_0000119>
        <ns2:IAO_0000118>Scapuloperoneal muscular dystrophy (disorder)</ns2:IAO_0000118>
        <ns2:IAO_0000118>Muscular Dystrophy, Emery-Dreifuss, X-Linked</ns2:IAO_0000118>
        <ns2:IAO_0000118>Muscular Dystrophy, Emery-Dreifuss, Autosomal Dominant</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:12755701</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:11973618</ns2:IAO_0000119>
        <ns2:IAO_0000119>SNOMEDCT:129620000</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15009215</ns2:IAO_0000119>
        <ns2:IAO_0000118>Emery-Dreifuss muscular dystrophy</ns2:IAO_0000118>
        <ns2:IAO_0000118>Scapuloilioperoneal Atrophy with Cardiopathy</ns2:IAO_0000118>
        <ns2:IAO_0000118>Emery-Dreifuss Muscular Dystrophy, Autosomal Recessive</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:12684533</ns2:IAO_0000119>
        <ns2:IAO_0000118>Muscular Dystrophy, Emery-Dreifuss Type</ns2:IAO_0000118>
        <ns2:IAO_0000118>Scapuloperoneal Syndrome, X Linked</ns2:IAO_0000118>
        <ns2:IAO_0000118>Benign scapuloperoneal muscular dystrophy with early contractures</ns2:IAO_0000118>
        <rdfs:comment>A heterogenous group of inherited muscular dystrophy without the involvement of nervous system. The disease is characterized by MUSCULAR ATROPHY; MUSCLE WEAKNESS; CONTRACTURE of the elbows; ACHILLES TENDON; and posterior cervical muscles; with or without cardiac features. There are several INHERITANCE PATTERNS including X-linked (X CHROMOSOME), autosomal dominant, and autosomal recessive gene mutations.</rdfs:comment>
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    <!-- http://www.ebi.ac.uk/efo/EFO_0000757 -->

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        <rdfs:label>muscular dystrophy</rdfs:label>
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