TEMPLATE CKM - Pharmacogenetic phenotype (CKM - Pharmacogenetic phenotype)

TEMPLATE IDCKM - Pharmacogenetic phenotype
ConceptCKM - Pharmacogenetic phenotype
DescriptionNot Specified
PurposeNot Specified
References
Authorsdate: 2023-03-07
Other Details Languagedate: 2023-03-07
OtherDetails Language Independent{licence=This work is licensed under the Creative Commons Attribution-ShareAlike 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-sa/4.0/., custodian_organisation=openEHR Foundation, PARENT:MD5-CAM-1.0.1=70DE7D6A08DA0E7CEC7E6860EE6931FF, original_language=ISO_639-1::en, original_namespace=org.openehr, original_publisher=openEHR Foundation, custodian_namespace=org.openehr, MD5-CAM-1.0.1=e9122f43f04b143492da00fd8d20ee8e, sem_ver=0.1.0}
Language useden
Citeable Identifier1051.57.299
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  • Normal metaboliser 
  • Rapid metaboliser 
  • Ultrarapid metaboliser 
  • Intermediate metaboliser 
  • Poor metaboliser 
  • Increased function 
  • Decreased function 
  • Normal function 
  • Poor function 
, extendedValues=null], ResourceSimplifiedHierarchyItem [path=[openEHR-EHR-EVALUATION.pharmacogenetic_phenotype.v0]/data[at0001]/items[at0002], code=at0002, itemType=ELEMENT, level=2, text=Phenotype term, description=A single 'pre-coordinated' term which includes the gene/enzyme name and the metaboliser status., comment=This may need to be pre-computed to support clinical systems which require pre-coordinated SNOMED-CT terms to support CDSS., uncommonOntologyItems=null, occurencesFormal=null, occurencesText=null, cardinalityFormal=null, cardinalityText=null, subCardinalityFormal=null, subCardinalityText=null, dataType=DV_CODED_TEXT, bindings=null, values=Terminology: http://snomed.info/sct
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