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    <!-- http://purl.obolibrary.org/obo/MONDO_0003847 -->

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        <rdfs:label>hereditary disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0013125 -->

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        <rdfs:label>CLAPO syndrome</rdfs:label>
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        <ns4:curated_content_resource rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://www.malacards.org/card/capillary_malformation_of_the_lower_lip_lymphatic_malformation_of_face_and_neck_asymmetry_of_face_and_limbs_and_partial_generalized_overgrowth</ns4:curated_content_resource>
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        <oboInOwl:hasDbXref>SCTID:717765001</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>MESH:C567763</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>CLAPO syndrome is a newly described syndrome consisting of capillary malformation of the lower lip (C), lymphatic malformation of the face and neck (L), asymmetry of face and limbs (A) and partial or generalized overgrowth (O).</ns3:IAO_0000115>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0019716 -->

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