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    <!-- http://www.ebi.ac.uk/efo/EFO_0000310 -->

    <Class rdf:about="http://www.ebi.ac.uk/efo/EFO_0000310">
        <rdfs:label>limb-girdle muscular dystrophy</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://www.ebi.ac.uk/efo/EFO_0000757"/>
        <ns2:IAO_0000118>Leyden-Mbius muscular dystrophy</ns2:IAO_0000118>
        <rdfs:seeAlso>URI: http://www.ebi.ac.uk/cellline#obsolete_calpainopathy</rdfs:seeAlso>
        <ns2:IAO_0000119>MSH:D049288</ns2:IAO_0000119>
        <ns2:IAO_0000118>Muscular Dystrophies, Limb Girdle</ns2:IAO_0000118>
        <ns2:IAO_0000231>duplicate of limb-girdle muscular dystrophy EFO_0000758</ns2:IAO_0000231>
        <ns2:IAO_0000118>Leyden-MÃƒÆ’Ã‚Â¶bius muscular dystrophy</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:12032588</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:11741828</ns2:IAO_0000119>
        <ns2:IAO_0000119>SNOMEDCT:93153005</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15385448</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:14981167</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:16344347</ns2:IAO_0000119>
        <ns2:IAO_0000118>Leyden-Mobius muscular dystrophy</ns2:IAO_0000118>
        <ns2:IAO_0000119>DOID:11724</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15351423</ns2:IAO_0000119>
        <ns2:IAO_0000118>limb girdle muscular dystrophy</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:11822024</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:11891182</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:15087111</ns2:IAO_0000119>
        <ns2:IAO_0000119>GeneRIF:12428213</ns2:IAO_0000119>
        <ns2:IAO_0000118>limb-girdle muscular dystrophy type 2A</ns2:IAO_0000118>
        <ns2:IAO_0000118>Limb-girdle muscular dystrophy (disorder)</ns2:IAO_0000118>
        <ns2:IAO_0000118>obsolete_calpainopathy</ns2:IAO_0000118>
        <ns2:IAO_0000119>GeneRIF:12499399</ns2:IAO_0000119>
        <ns2:IAO_0000117>James Malone</ns2:IAO_0000117>
        <ns2:IAO_0000119>GeneRIF:14600260</ns2:IAO_0000119>
        <rdfs:comment>A heterogenous group of inherited muscular dystrophy that can be autosomal dominant or autosomal recessive. There are many forms (called LGMDs) involving genes encoding muscle membrane proteins such as the sarcoglycan (SARCOGLYCANS) complex that interacts with DYSTROPHIN. The disease is characterized by progressing wasting and weakness of the proximal muscles of arms and legs around the HIPS and SHOULDERS (the pelvic and shoulder girdles).</rdfs:comment>
    </Class>
    


    <!-- http://www.ebi.ac.uk/efo/EFO_0000757 -->

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