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    <!-- http://purl.obolibrary.org/obo/RO_0004020 -->

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        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">disease has basis in dysfunction of</rdfs:label>
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    <!-- http://identifiers.org/hgnc/3690 -->

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        <rdfs:label>FGFR3</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0000426 -->

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    <!-- http://purl.obolibrary.org/obo/MONDO_0005363 -->

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        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">focal segmental glomerulosclerosis</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0012833 -->

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        <ns3:IAO_0000115 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Crouzon syndrome with acanthosis nigricans (CAN) is a very rare, clinically heterogeneous form of faciocraniostenosis with Crouzon-like features and premature synostosis of cranial sutures (Crouzon disease), associated with acanthosis nigricans (AN).</ns3:IAO_0000115>
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