This page is part of the FHIR Specification (v1.0.0: DSTU 2 Ballot 3). The current version which supercedes this version is 5.0.0. For a full list of available versions, see the Directory of published versions
ABCB4 gene mutation analysis - variant 4 (id = "genetics-example3-mutationlist-4")
<Observation xmlns="http://hl7.org/fhir"> <id value="genetics-example3-mutationlist-4"/> <text><status value="generated"/><div xmlns="http://www.w3.org/1999/xhtml"><p><b>Generated Narrative with Details</b></p><p><b>id</b>: genetics-example3-mutationlist-4</p><p><b>status</b>: final</p><p><b>code</b>: ABCB4 gene mutation analysis <span>(Details : {LOINC code '49874-1' = 'ABCB4 gene mutation analysis in Blood or Tissue by Molecular genetics method Narrative', given as 'ABCB4 gene mutation analysis'})</span></p><p><b>subject</b>: <a>Molecular Lab Patient ID: HOSP-23456</a></p><p><b>performer</b>: <a>Molecular Diagnostic Laboratory</a></p><p><b>specimen</b>: <a>Molecular Specimen ID: MLD45-Z4-1234</a></p><h3>Components</h3><table><tr><td>-</td><td><b>Code</b></td><td><b>Value[x]</b></td></tr><tr><td>*</td><td>Genetic disease sequence variation interpretation <span>(Details : {LOINC code '53037-8' = 'Genetic disease sequence variation interpretation [interpretation] in Blood or Tissue by Molecular genetics method', given as 'Genetic disease sequence variation interpretation'})</span></td><td>Benign <span>(Details : {http://www.genenames.org code 'LA6675-8' = '??', given as 'Benign'})</span></td></tr></table></div></text><extension url="http://hl7.org/fhir/StructureDefinition/geneticsDNARegionName"> <valueString value="intron 26"/> </extension> <extension url="http://hl7.org/fhir/StructureDefinition/geneticsVariationId"> <valueCodeableConcept> <coding> <system value="http://www.ncbi.nlm.nih.gov/projects/SNP"/> <code value="31653"/> <display value="c.3487-16T>C"/> </coding> </valueCodeableConcept> </extension> <status value="final"/> <code> <coding> <system value="http://loinc.org"/> <code value="49874-1"/> <display value="ABCB4 gene mutation analysis"/> </coding> </code> <subject> <reference value="Patient/genetics-example2"/> <display value="Molecular Lab Patient ID: HOSP-23456"/> </subject> <performer> <reference value="Practitioner/genetics-example2"/> <display value="Molecular Diagnostic Laboratory"/> </performer> <specimen> <reference value="Specimen/genetics-example2"/> <display value="Molecular Specimen ID: MLD45-Z4-1234"/> </specimen> <component> <code> <coding> <system value="http://loinc.org"/> <code value="53037-8"/> <display value="Genetic disease sequence variation interpretation"/> </coding> </code> <valueCodeableConcept> <coding> <system value="http://www.genenames.org"/> <code value="LA6675-8"/> <display value="Benign"/> </coding> </valueCodeableConcept> </component> </Observation>
Usage note: every effort has been made to ensure that the examples are correct and useful, but they are not a normative part of the specification.