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    <!-- http://purl.obolibrary.org/obo/HP_0003812 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HP_0003812">
        <rdfs:label>Phenotypic variability</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/HP_0012823"/>
        <rdfs:comment>This term can be applied to disease entities but not to individuals. It may be made obsolete in future versions of the HPO.</rdfs:comment>
        <oboInOwl:hasExactSynonym>Highly variable phenotype, even within families</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Clinical heterogeneity</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Variable phenotypic severity</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Highly variable phenotype and severity</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C1839039</oboInOwl:hasDbXref>
        <oboInOwl:hasAlternativeId>HP:0003815</oboInOwl:hasAlternativeId>
        <oboInOwl:hasExactSynonym>Highly variable clinical phenotype</oboInOwl:hasExactSynonym>
        <oboInOwl:hasAlternativeId>HP:0003813</oboInOwl:hasAlternativeId>
        <oboInOwl:hasDbXref>UMLS:C1850667</oboInOwl:hasDbXref>
        <ns3:IAO_0000115>A variability of phenotypic features.</ns3:IAO_0000115>
        <oboInOwl:hasExactSynonym>Highly variable phenotype</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>UMLS:C1837514</oboInOwl:hasDbXref>
        <oboInOwl:hasAlternativeId>HP:0003822</oboInOwl:hasAlternativeId>
        <oboInOwl:hasExactSynonym>Variable phenotype</oboInOwl:hasExactSynonym>
        <oboInOwl:hasAlternativeId>HP:0003821</oboInOwl:hasAlternativeId>
        <oboInOwl:hasDbXref>UMLS:C1866210</oboInOwl:hasDbXref>
        <oboInOwl:id>HP:0003812</oboInOwl:id>
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    <!-- http://purl.obolibrary.org/obo/HP_0012823 -->

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