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    <!-- http://purl.obolibrary.org/obo/MONDO_0000577 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0000577">
        <rdfs:label>congenital anemia</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0000863 -->

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        <rdfs:label>myopathy, lactic acidosis, and sideroblastic anemia</rdfs:label>
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        <oboInOwl:hasRelatedSynonym>sideroblastic anemia and mitochondrial myopathy</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>myopathy, lactic acidosis, and siderblastic anemia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C1838103</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0000863</oboInOwl:id>
        <oboInOwl:hasDbXref>DOID:0080099</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C536101</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>myopathy, lactic acidosis, and siderblastic anaemia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>mitochondrial myopathy and sideroblastic anaemia</oboInOwl:hasExactSynonym>
        <ns3:IAO_0000115>Mitochondrial myopathy and sideroblastic anemia belongs to the heterogeneous family of metabolic myopathies. It is characterized by progressive exercise intolerance manifesting in childhood, onset of sideroblastic anemia around adolescence, lactic acidaemia, and mitochondrial myopathy.</ns3:IAO_0000115>
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        <oboInOwl:hasRelatedSynonym>sideroblastic anaemia and mitochondrial myopathy</oboInOwl:hasRelatedSynonym>
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        <oboInOwl:hasDbXref>SCTID:724138007</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0003885</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>myopathy with lactic acidosis and sideroblastic anemia</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>mitochondrial myopathy and sideroblastic anemia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIMPS:600462</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>MSA</oboInOwl:hasExactSynonym>
        <oboInOwl:hasRelatedSynonym>myopathy with lactic acidosis and sideroblastic anaemia</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>Orphanet:2598</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>myopathy, lactic acidosis and sideroblastic anaemia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:373888</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0009637 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0009637">
        <rdfs:label>inborn mitochondrial myopathy</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016387 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0016387">
        <rdfs:label>mitochondrial oxidative phosphorylation disorder</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0020099 -->

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        <rdfs:label>inherited sideroblastic anemia</rdfs:label>
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