ARCHETYPE Phenopacket phenotypic feature (openEHR-EHR-CLUSTER.pp_phenotypic_feature.v0)

ARCHETYPE IDopenEHR-EHR-CLUSTER.pp_phenotypic_feature.v0
ConceptPhenopacket phenotypic feature
DescriptionPhenotypic feature
Purpose
References
Copyright© openEHR Foundation
AuthorsAuthor name: Heather Leslie
Organisation: Atomica Informatics
Email: heather.leslie@atomicainformatics.com
Date originally authored: 2019-09-25
Other Details LanguageAuthor name: Heather Leslie
Organisation: Atomica Informatics
Email: heather.leslie@atomicainformatics.com
Date originally authored: 2019-09-25
Other Details (Language Independent)
  • Licence: This work is licensed under the Creative Commons Attribution-ShareAlike 3.0 License. To view a copy of this license, visit http://creativecommons.org/licenses/by-sa/3.0/.
  • Custodian Organisation: openEHR Foundation
  • Original Namespace: org.openehr
  • Original Publisher: openEHR Foundation
  • Custodian Namespace: org.openehr
  • MD5-CAM-1.0.1: E9291020A69DDE3E146C4E2851A40437
  • Build Uid: 00834722-32a2-4036-8d60-7fd940e40f97
  • Revision: 0.0.1-alpha
Keywords
Lifecyclein_development
UID15182932-16a5-425a-9bda-bca460a116a0
Language useden
Citeable Identifier1013.1.4145
Revision Number0.0.1-alpha
items
descriptiondescription: Human-readable verbiage NOT for structured text.
typetype: *
For example: "HP::0000520|Proptosis".
negatednegated: *
Assumed value: false
severityseverity: Description of the severity of the feature described in type representing HP:0012824.
For example: "HP::0012825|Mild".
modifiermodifier: representing one or more terms from HP:0012823
onsetonset: ??The age group in which disease manifestations appear.
HP:0003674 HP:0011462 For example: "HP::0003577|Congenital onset".
evidenceevidence: *
The evidence for an assertion of the observation of a type.
Include:
openEHR-EHR-CLUSTER.pp_evidence.v0
Other contributors
Translators