Preferred Name |
Phenotypic variability |
|
Synonyms |
Variable phenotypic severity Variable phenotype Clinical heterogeneity Highly variable clinical phenotype Highly variable phenotype, even within families Highly variable phenotype Highly variable phenotype and severity |
|
Definitions |
This term can be applied to disease entities but not to individuals. It may be made obsolete in future versions of the HPO. A variability of phenotypic features. |
|
ID |
http://purl.obolibrary.org/obo/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. |
|
database_cross_reference |
UMLS:C1839039 UMLS:C1850667 UMLS:C1866210 UMLS:C1837514 |
|
definition |
A variability of phenotypic features. |
|
has_alternative_id |
HP:0003813 HP:0003821 HP:0003815 HP:0003822 |
|
has_exact_synonym |
Variable phenotypic severity Variable phenotype Clinical heterogeneity Highly variable clinical phenotype Highly variable phenotype, even within families Highly variable phenotype Highly variable phenotype and severity |
|
has_obo_namespace |
human_phenotype |
|
id |
HP:0003812 |
|
label |
Phenotypic variability |
|
notation |
HP:0003812 |
|
prefLabel |
Phenotypic variability |
|
treeView | ||
subClassOf |
Delete | Mapping To | Ontology | Source |
---|---|---|---|
http://purl.obolibrary.org/obo/HP_0003812 | UPHENO | SAME_URI | |
http://purl.org/obo/owl/HP#HP_0003812 | BDO | LOOM | |
http://purl.obolibrary.org/obo/HP_0003812 | UPHENO | LOOM |