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    <!-- http://purl.obolibrary.org/obo/MONDO_0017687 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0017687">
        <rdfs:label>disorder of neutral amino acid transport</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0019216"/>
        <ns3:IAO_0000115>An inherited metabolic disease that is has its basis in the disruption of neutral amino acid transport.</ns3:IAO_0000115>
        <oboInOwl:hasDbXref>MEDGEN:1863589</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>inborn neutral amino acid transport disorder</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>Orphanet:308451</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>rare inborn error of neutral amino acid transport</oboInOwl:hasExactSynonym>
        <oboInOwl:id>MONDO:0017687</oboInOwl:id>
        <oboInOwl:hasExactSynonym>inborn error of neutral amino acid transport</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C5848149</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0021305</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019216 -->

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