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        <rdf:type rdf:resource="http://www.w3.org/2002/07/owl#TransitiveProperty"/>
        <rdfs:label>has material basis in germline mutation in</rdfs:label>
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    <!-- http://identifiers.org/hgnc/6091 -->

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        <rdfs:label>INSR</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0002254 -->

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        <rdfs:label>syndromic disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0005015 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0005015">
        <rdfs:label>diabetes mellitus</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0006025 -->

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        <rdfs:label>autosomal recessive disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0009517 -->

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        <rdfs:label>Donohue syndrome</rdfs:label>
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        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/1567</ns5:IAO_0000233>
        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/5723</ns5:IAO_0000233>
        <ns3:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/donohue_syndrome</ns3:curated_content_resource>
        <oboInOwl:hasDbXref>Orphanet:508</oboInOwl:hasDbXref>
        <ns5:IAO_0000115>Leprechaunism is a congenital form of extreme insulin resistance (a group of syndromes that also includes Rabson-Mensenhall syndrome, type A insulin-resistance syndrome, and acquired type B insulin-resistance syndrome) characterized by intrauterine and mainly postnatal severe growth retardation.</ns5:IAO_0000115>
        <oboInOwl:hasDbXref>NCIT:C84676</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Donohue syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Leprechaunism</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>leprechaunism</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>MEDGEN:82708</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:0050470</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0009517</oboInOwl:id>
        <oboInOwl:hasDbXref>UMLS:C0265344</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0006885</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NORD:1361</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D056731</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>ICD9:259.8</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>OMIM:246200</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015161 -->

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        <rdfs:label>multiple congenital anomalies/dysmorphic syndrome without intellectual disability</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015333 -->

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        <rdfs:label>progeroid syndrome</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019280 -->

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        <rdfs:label>hypertrichosis</rdfs:label>
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