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- HP_0003812 IAO_0000115 "A variability of phenotypic features." @default.
- HP_0003812 normalizedInformationContent "95.413332725061409" @default.
- HP_0003812 referenceCount "2" @default.
- HP_0003812 hasAlternativeId "HP:0003813" @default.
- HP_0003812 hasAlternativeId "HP:0003815" @default.
- HP_0003812 hasAlternativeId "HP:0003821" @default.
- HP_0003812 hasAlternativeId "HP:0003822" @default.
- HP_0003812 hasDbXref "UMLS:C1837514" @default.
- HP_0003812 hasDbXref "UMLS:C1839039" @default.
- HP_0003812 hasDbXref "UMLS:C1850667" @default.
- HP_0003812 hasDbXref "UMLS:C1866210" @default.
- HP_0003812 hasExactSynonym "Clinical heterogeneity" @default.
- HP_0003812 hasExactSynonym "Highly variable clinical phenotype" @default.
- HP_0003812 hasExactSynonym "Highly variable phenotype and severity" @default.
- HP_0003812 hasExactSynonym "Highly variable phenotype" @default.
- HP_0003812 hasExactSynonym "Highly variable phenotype, even within families" @default.
- HP_0003812 hasExactSynonym "Variable phenotype" @default.
- HP_0003812 hasExactSynonym "Variable phenotypic severity" @default.
- HP_0003812 id "HP:0003812" @default.
- HP_0003812 type Class @default.
- HP_0003812 comment "This term can be applied to disease entities but not to individuals. It may be made obsolete in future versions of the HPO." @default.
- HP_0003812 isDefinedBy hp.owl @default.
- HP_0003812 label "Phenotypic variability" @default.
- HP_0003812 subClassOf HP_0000001 @default.
- HP_0003812 subClassOf HP_0003812 @default.
- HP_0003812 subClassOf HP_0012823 @default.
- HP_0003812 category Attribute @default.
- HP_0003812 category ClinicalAttribute @default.
- HP_0003812 category ClinicalModifier @default.
- HP_0003812 category Entity @default.
- HP_0003812 category NamedThing @default.
- HP_0003812 category OntologyClass @default.