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        <rdfs:label>disease has basis in disruption of</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/GO_0070330 -->

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        <rdfs:label>aromatase activity</rdfs:label>
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        <rdfs:label>reproductive system disorder</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0007690 -->

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        <rdfs:label>aromatase excess syndrome</rdfs:label>
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        <ns3:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/aromatase_excess_syndrome</ns3:curated_content_resource>
        <oboInOwl:hasDbXref>ICD9:259.8</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>familial hyperestrogenism</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>AEXS</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C1970109</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MEDGEN:409989</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>gynecomastia, familial, due to increased aromatase activity</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>SCTID:709075008</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>hereditary prepubertal gynecomastia</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>increased aromatase activity</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>GARD:0012494</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:0090122</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>aromatase excess syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>icd11.foundation:191989744</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:C000591739</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>OMIM:139300</oboInOwl:hasDbXref>
        <ns5:IAO_0000115>Aromatase excess syndrome is a rare, genetic endocrine disease characterized by increased levels of estrogen due to elevated extraglandular aromatase activity. Males present with heterosexual precocious puberty which manifests with pre- or peripubertal onset of gynecomastia, premature growth spurt, accelerated bone maturation resulting in decreased adult stature, and may present mild hypogonadotropic hypogonadism. Female patients may have isosexual precocious puberty or not have any manifestations at all.</ns5:IAO_0000115>
        <oboInOwl:hasExactSynonym>gynecomastia, hereditary</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>Orphanet:178345</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015791 -->

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        <rdfs:label>peripheral precocious puberty</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0016072 -->

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        <rdfs:label>obsolete anomaly of puberty or/and menstrual cycle of genetic origin</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0018561 -->

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        <rdfs:label>precocious puberty in female</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019052 -->

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        <rdfs:label>inborn errors of metabolism</rdfs:label>
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