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        <rdfs:label>has material basis in germline mutation in</rdfs:label>
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    <!-- http://identifiers.org/hgnc/5209 -->

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        <rdfs:label>HSD11B2</rdfs:label>
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        <rdfs:label>adrenal gland disorder</rdfs:label>
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        <rdfs:label>steroid inherited metabolic disorder</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0006640 -->

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        <rdfs:label>adrenal gland hyperfunction</rdfs:label>
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        <rdfs:label>apparent mineralocorticoid excess</rdfs:label>
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        <oboInOwl:hasDbXref>DOID:0090121</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0342488</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>11-beta-hydroxysteroid dehydrogenase deficiency type 2</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>NCIT:C131083</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>cortisol 11-beta-ketoreductase deficiency</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasExactSynonym>11 Beta-hydroxysteroid dehydrogenase type 2 deficiency</oboInOwl:hasExactSynonym>
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        <oboInOwl:hasDbXref>SCTID:703256004</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>icd11.foundation:1737310323</oboInOwl:hasDbXref>
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        <oboInOwl:hasRelatedSynonym>AME 1</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>Ulick syndrome</oboInOwl:hasExactSynonym>
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        <rdfs:label>syndromic dyslipidemia</rdfs:label>
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