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    <!-- http://purl.obolibrary.org/obo/MONDO_0003778 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0003778">
        <rdfs:label>inborn error of immunity</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0100210 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0100210">
        <rdfs:label>growth hormone insensitivity syndrome with immune dysregulation</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_1060224 -->

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        <rdfs:label>STAT5 haploinsufficiency</rdfs:label>
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        <ns3:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/9961</ns3:IAO_0000233>
        <oboInOwl:id>MONDO:1060224</oboInOwl:id>
        <oboInOwl:hasDbXref>GARD:0015006</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>STAT5A/5B haploinsufficiency</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>STAT5 deficiency (haploinsufficient)</oboInOwl:hasExactSynonym>
        <ns3:IAO_0000115>A condition characterized by haploinsufficient levels of STAT5 protein due to reduced copy number or expression of the STAT5A and/or STAT5B genes, with consequent attenuation of STAT5-mediated cytokine signalling (including IL-7 and growth hormone pathways). This condition is also associated with altered lymphocyte homeostasis and modified susceptibility to lymphoma development.</ns3:IAO_0000115>
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