FHIR IG analytics| Package | de.medizininformatikinitiative.kerndatensatz.molgen |
| Resource Type | ServiceRequest |
| Id | ServiceRequest-mii-exa-molgen-anforderung-wes.json |
| FHIR Version | R4 |
No resources found
No resources found
Note: links and images are rebased to the (stated) source
English
Generated Narrative: ServiceRequest mii-exa-molgen-anforderung-wes
Profile: MII PR MolGen Anforderung genetischer Test version: 2027.0.0-ballot.1
status: Completed
intent: Order
code: Whole exome sequence analysis in Blood or Tissue by Molecular genetics method
subject: Maja Julia Van-der-Dussen (official) Female, DoB: 1968-09-19 ( Medical record number (use: usual, ))
authoredOn: 2024-01-10
requester: Practitioner Klaus Müller
reasonCode: Unklare Entwicklungsverzögerung mit Dysmorphiezeichen, V.a. genetisches Syndrom nach unauffälliger Chromosomenanalyse und Array-CGH
German
Generated Narrative: ServiceRequest mii-exa-molgen-anforderung-wes
Profile: MII PR MolGen Anforderung genetischer Test version: 2027.0.0-ballot.1
status: Completed
intent: Order
code: Whole exome sequence analysis in Blood or Tissue by Molecular genetics method
subject: Maja Julia Van-der-Dussen (official) Female, DoB: 1968-09-19 ( Krankenaktennummer (use: usual, ))
authoredOn: 2024-01-10
requester: Practitioner Klaus Müller
reasonCode: Unklare Entwicklungsverzögerung mit Dysmorphiezeichen, V.a. genetisches Syndrom nach unauffälliger Chromosomenanalyse und Array-CGH
{
"resourceType": "ServiceRequest",
"id": "mii-exa-molgen-anforderung-wes",
"meta": {
"profile": [
"https://www.medizininformatik-initiative.de/fhir/ext/modul-molgen/StructureDefinition/anforderung-genetischer-test|2027.0.0-ballot.1"
]
},
"text": {
"status": "generated",
"div": "<!-- snip (see above) -->"
},
"status": "completed",
"intent": "order",
"code": {
"coding": [
{
"system": "http://loinc.org",
"code": "86205-2",
"display": "Whole exome sequence analysis in Blood or Tissue by Molecular genetics method"
}
]
},
"subject": {
"reference": "Patient/mii-exa-molgen-patient"
},
"authoredOn": "2024-01-10",
"requester": {
"reference": "Practitioner/mii-exa-molgen-practitioner-ordering"
},
"reasonCode": [
{
"coding": [
{
"system": "http://snomed.info/sct",
"code": "224958001",
"display": "Global developmental delay"
}
],
"text": "Unklare Entwicklungsverzögerung mit Dysmorphiezeichen, V.a. genetisches Syndrom nach unauffälliger Chromosomenanalyse und Array-CGH"
}
]
}