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    <!-- http://purl.obolibrary.org/obo/MONDO_0002412 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0002412">
        <rdfs:label>disorder of glycogen metabolism</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0010392 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0010392">
        <rdfs:label>glycogen storage disease due to phosphoglycerate kinase 1 deficiency</rdfs:label>
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        <ns4:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/4985</ns4:IAO_0000233>
        <ns2:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/phosphoglycerate_kinase_1_deficiency</ns2:curated_content_resource>
        <oboInOwl:id>MONDO:0010392</oboInOwl:id>
        <oboInOwl:hasExactSynonym>glycogen storage disease due to phosphoglycerate kinase 1 deficiency</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>NCIT:C126738</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:300653</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>PGK1 glycogen storage disease</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>glycogenosis due to phosphoglycerate kinase 1 deficiency</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>DOID:0111933</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C1970848</oboInOwl:hasDbXref>
        <ns4:IAO_0000115>Phosphoglycerate kinase (PGK) deficiency is a metabolic disorder characterized by variable combinations of nonspherocytic hemolytic anemia, myopathy, and various central nervous system abnormalities.</ns4:IAO_0000115>
        <oboInOwl:hasDbXref>MESH:C567067</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>Phosphoglycerate kinase deficiency</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>NORD:1577</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>GSD due to phosphoglycerate kinase 1 deficiency</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Phosphoglycerate Kinase Deficiency</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0007389</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>PGK deficiency</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>glycogen storage disease caused by mutation in PGK1</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>Orphanet:713</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>icd11.foundation:1396572570</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NANDO:1200831</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:410166</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016118 -->

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        <rdfs:label>obsolete muscular glycogenosis</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0017688 -->

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        <rdfs:label>disorder of glycolysis</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0020585 -->

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        <rdfs:label>anemia due to erythrocyte enzyme disorder</rdfs:label>
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        <rdfs:label>obsolete_glycogen storage disease due to phosphoglycerate kinase 1 deficiency</rdfs:label>
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