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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/391 -->

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        <rdfs:label>AKT1</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0008318 -->

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        <rdfs:label>Proteus syndrome</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0017623"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MONDO_0018230"/>
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        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/4521</ns5:IAO_0000233>
        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/4948</ns5:IAO_0000233>
        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6751</ns5:IAO_0000233>
        <ns5:IAO_0000233 rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://github.com/monarch-initiative/mondo/issues/6877</ns5:IAO_0000233>
        <ns3:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/proteus_syndrome</ns3:curated_content_resource>
        <oboInOwl:hasExactSynonym>proteus syndrome, somatic</oboInOwl:hasExactSynonym>
        <ns5:IAO_0000115>Proteus syndrome (PS) is a very rare and complex hamartomatous overgrowth disorder characterized by progressive overgrowth of the skeleton, skin, adipose, and central nervous systems.</ns5:IAO_0000115>
        <oboInOwl:hasDbXref>icd11.foundation:760267333</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Proteus syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>OMIM:176920</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>Elattoproteus syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>ICD9:759.89</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>partial gigantism-nevi-hemihypertrophy-macrocephaly syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:id>MONDO:0008318</oboInOwl:id>
        <oboInOwl:hasDbXref>NCIT:C85032</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>DOID:13482</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>Orphanet:744</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NORD:1622</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>partial gigantism of hands and feet, nevi, hemihypertrophy, macrocephaly</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>MEDGEN:39008</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Wiedemann&#39;s syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C0085261</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0007475</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>MESH:D016715</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>gigantism, partial, of hands and feet, nevi, hemihypertrophy, and macrocephaly</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasRelatedSynonym>hemihypertrophy and macrocephaly</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasDbXref>SCTID:23150001</oboInOwl:hasDbXref>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0015501 -->

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        <rdfs:label>obsolete syndrome or malformation associated with head and neck malformations</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0017623 -->

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        <rdfs:label>PTEN hamartoma tumor syndrome</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0018230 -->

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        <rdfs:label>skeletal dysplasia</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019716 -->

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        <rdfs:label>overgrowth syndrome</rdfs:label>
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