FHIR IG analytics| Package | de.medizininformatikinitiative.kerndatensatz.seltene |
| Resource Type | DiagnosticReport |
| Id | DiagnosticReport-molgen-brca-panel.json |
| FHIR Version | R4 |
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No narrative content found in resource
{
"resourceType": "DiagnosticReport",
"id": "molgen-brca-panel",
"status": "final",
"category": [
{
"coding": [
{
"system": "http://terminology.hl7.org/CodeSystem/v2-0074",
"code": "LAB",
"display": "Laboratory"
}
]
}
],
"code": {
"coding": [
{
"system": "http://loinc.org",
"code": "81247-9",
"display": "Master HL7 genetic variant reporting panel"
}
]
},
"subject": {
"reference": "Patient/example"
},
"effectiveDateTime": "2024-11-01",
"result": [
{
"reference": "Observation/molgen-variant-brca1-pathogenic"
}
],
"conclusion": "Pathogene Variante c.68_69del (p.Glu23Valfs*17) in BRCA1 nachgewiesen. Diese Frameshift-Mutation führt zu einem vorzeitigen Stopcodon. Erhöhtes Risiko für Mamma- und Ovarialkarzinom. Lebenszeitrisiko Mammakarzinom: 60-72%, Ovarialkarzinom: 40-44%.",
"conclusionCode": [
{
"coding": [
{
"system": "http://omim.org",
"code": "604370",
"display": "Breast-ovarian cancer, familial, 1"
}
]
}
]
}