FHIR IG analytics| Package | de.medizininformatikinitiative.kerndatensatz.molgen |
| Resource Type | Observation |
| Id | Observation-mii-exa-molgen-diagnostische-implikation-cnv-4.json |
| FHIR Version | R4 |
No resources found
No resources found
Note: links and images are rebased to the (stated) source
English
Generated Narrative: Observation mii-exa-molgen-diagnostische-implikation-cnv-4
Profiles: MII PR MolGen Diagnostische Implikation version: 2027.0.0-ballot.1, Diagnostic Implication version: 3.0.0
status: Final
category: Laboratory, Genetics
code: Diagnostic Implication
subject: Melanie Marie Müller (official) Female, DoB: 2021-09-19 ( Medical record number (use: usual, ))
effective: 2022-03-16
performer: Practitioner Dr. Daniel Schmidt(official)
derivedFrom: Observation Genetic variant assessment
component
code: Conclusion Text
value: onkogene Veränderung
component
code: Genetic variation clinical significance [Imp]
value: Likely pathogenic
German
Generated Narrative: Observation mii-exa-molgen-diagnostische-implikation-cnv-4
Profiles: MII PR MolGen Diagnostische Implikation version: 2027.0.0-ballot.1, Diagnostic Implication version: 3.0.0
status: Final
category: Laboratory, Genetik
code: Diagnostic Implication
subject: Melanie Marie Müller (official) Female, DoB: 2021-09-19 ( Krankenaktennummer (use: usual, ))
effective: 2022-03-16
performer: Practitioner Dr. Daniel Schmidt(official)
derivedFrom: Observation Genetic variant assessment
component
code: Conclusion Text
value: onkogene Veränderung
component
code: Genetic variation clinical significance [Imp]
value: Likely pathogenic
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"meta": {
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"http://hl7.org/fhir/uv/genomics-reporting/StructureDefinition/diagnostic-implication|3.0.0"
]
},
"text": {
"status": "generated",
"div": "<!-- snip (see above) -->"
},
"status": "final",
"category": [
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"code": "laboratory",
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"code": "GE"
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],
"code": {
"coding": [
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"code": "diagnostic-implication",
"display": "Diagnostic Implication"
}
]
},
"subject": {
"reference": "Patient/mii-exa-molgen-patient-2"
},
"effectiveDateTime": "2022-03-16",
"performer": [
{
"reference": "Practitioner/mii-exa-molgen-practitioner-lab"
}
],
"derivedFrom": [
{
"reference": "Observation/mii-exa-molgen-variante-cnv-4"
}
],
"component": [
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"code": "conclusion-string"
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]
},
"valueString": "onkogene Veränderung "
},
{
"code": {
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"code": "53037-8",
"display": "Genetic variation clinical significance [Imp]"
}
]
},
"valueCodeableConcept": {
"coding": [
{
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"code": "LA26332-9",
"display": "Likely pathogenic"
}
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]
}