This page is part of the FHIR Specification (v1.0.2: DSTU 2). 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 2
{ "resourceType": "Observation", "id": "genetics-example3-mutationlist-2", "text": { "status": "generated", "div": "<div><p><b>Generated Narrative with Details</b></p><p><b>id</b>: genetics-example3-mutationlist-2</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>" }, "extension": [ { "url": "http://hl7.org/fhir/StructureDefinition/geneticsDNARegionName", "valueString": "Exon 6" }, { "url": "http://hl7.org/fhir/StructureDefinition/geneticsAminoAcidChange", "valueString": "p.N168N" }, { "url": "http://hl7.org/fhir/StructureDefinition/geneticsVariationId", "valueCodeableConcept": { "coding": [ { "system": "http://www.ncbi.nlm.nih.gov/projects/SNP", "code": "1202283", "display": "c.181T>G" } ] } } ], "status": "final", "code": { "coding": [ { "system": "http://loinc.org", "code": "49874-1", "display": "ABCB4 gene mutation analysis" } ] }, "subject": { "reference": "Patient/genetics-example2", "display": "Molecular Lab Patient ID: HOSP-23456" }, "performer": [ { "reference": "Practitioner/genetics-example2", "display": "Molecular Diagnostic Laboratory" } ], "specimen": { "reference": "Specimen/genetics-example2", "display": "Molecular Specimen ID: MLD45-Z4-1234" }, "component": [ { "code": { "coding": [ { "system": "http://loinc.org", "code": "53037-8", "display": "Genetic disease sequence variation interpretation" } ] }, "valueCodeableConcept": { "coding": [ { "system": "http://www.genenames.org", "code": "LA6675-8", "display": "Benign" } ] } } ] }
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.