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    <!-- http://www.orpha.net/ORDO/Orphanet_308604 -->

    <Class rdf:about="http://www.orpha.net/ORDO/Orphanet_308604">
        <rdfs:label>Glycogen storage disease due to acid maltase deficiency, adult onset</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://www.orpha.net/ORDO/Orphanet_365"/>
        <oboInOwl:hasExactSynonym>Pompe disease, adult onset</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Alpha-1,4-glucosidase acid deficiency, adult onset</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>GSD due to acid maltase deficiency, adult onset</oboInOwl:hasExactSynonym>
        <ns4:definition_citation>orphanet</ns4:definition_citation>
        <ns3:IAO_0000115>Glycogen storage disease due to acid maltase deficiency, late onset (AMDL), a form of Glycogen storage disease due to acid maltase deficiency (AMD), a degenerative metabolic myopathy particularly affecting respiratory and skeletal muscles, is characterized by an accumulation of glycogen in lysosomes.</ns3:IAO_0000115>
        <oboInOwl:hasExactSynonym>glycogen storage disease ii, adult form</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>GSD type 2, adulte onset</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Glycogenosis due to acid maltase deficiency, adult onset</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>ICD10:E74.0</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Glycogenosis type 2, adult onset</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Glycogen storage disease type 2, adult onset</oboInOwl:hasExactSynonym>
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