Link

Type: PhenotypicFeature

URI: biolink:PhenotypicFeature

UPHENO:0001001

SIO:010056

WIKIDATA:Q169872


![img](http://yuml.me/diagram/nofunky;dir:TB/class/[EntityToPhenotypicFeatureAssociation]-%20object%201..1%3E[PhenotypicFeature id(i):string;name(i):label_type;category(i):category_type%20%2B],[DiseaseOrPhenotypicFeature]%5E-[PhenotypicFeature],[OrganismTaxon],[EntityToPhenotypicFeatureAssociation],[DiseaseOrPhenotypicFeature],[BiologicalEntity])

Identifier prefixes

  • HP
  • EFO
  • NCIT
  • UMLS
  • MEDDRA
  • MP
  • ZP
  • UPHENO
  • APO
  • FBcv
  • WBPhenotype
  • SNOMEDCT
  • MESH

Parents

  • is_a: DiseaseOrPhenotypicFeature - Either one of a disease or an individual phenotypic feature. Some knowledge resources such as Monarch treat these as distinct, others such as MESH conflate.

Referenced by class

Attributes

Inherited from named thing:

  • id REQ
    • Description: A unique identifier for a thing. Must be either a CURIE shorthand for a URI or a complete URI
    • range: String
    • in subsets: (translator_minimal)
  • name REQ
    • Description: A human-readable name for a thing
    • range: LabelType
    • in subsets: (translator_minimal)
  • category 1..*
    • Description: Name of the high level ontology class in which this entity is categorized. Corresponds to the label for the biolink entity type class. In a neo4j database this MAY correspond to the neo4j label tag
    • range: CategoryType
    • in subsets: (translator_minimal)

Inherited from thing with taxon:

  • in taxon 0..*
    • Description: connects a thing to a class representing a taxon
    • range: OrganismTaxon
    • in subsets: (translator_minimal)

Other properties

     
Aliases:   sign
    symptom
    phenotype
    trait
    endophenotype
Mappings:   UPHENO:0001001
    SIO:010056
    WIKIDATA:Q169872