MII IG Kerndatensatz-Modul Molekulargenetischer Befundbericht
2027.0.0-ballot.1 - Germany

This page is part of the MII IG Kerndatensatz-Modul Molekulargenetischer Befundbericht (v2027.0.0-ballot.1: Release) based on FHIR (HL7® FHIR® Standard) R4. This is the current published version. For a full list of available versions, see the Directory of published versions

: Anforderung Molekulargenetische Diagnose Familiäre Belastung für Brust- und Eierstockkrebs

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    <div xml:lang="en" lang="en"><hr/><p><b>English</b></p><hr/><p class="res-header-id"><b>Generated Narrative: ServiceRequest mii-exa-molgen-anforderung-trurisk-panel</b></p><a name="mii-exa-molgen-anforderung-trurisk-panel"> </a><a name="hcmii-exa-molgen-anforderung-trurisk-panel"> </a><div style="display: inline-block; background-color: #d9e0e7; padding: 6px; margin: 4px; border: 1px solid #8da1b4; border-radius: 5px; line-height: 60%"><p style="margin-bottom: 0px"/><p style="margin-bottom: 0px">Profile: <a href="StructureDefinition-mii-pr-molgen-anforderung-genetischer-test.html">MII PR MolGen Anforderung genetischer Test</a> version: 2027.0.0-ballot.1</p></div><p><b>identifier</b>: <code>https://www.charite.de/fhir/auftragsnummern</code>/gen_test_03</p><p><b>status</b>: Active</p><p><b>intent</b>: Order</p><p><b>category</b>: <span title="Codes:{http://snomed.info/sct 108252007}">Laboratory procedure (procedure)</span></p><p><b>code</b>: <span title="Codes:{http://snomed.info/sct 405825005}">Panelanalyse TruRisk®-V3 mit NGS basierter CNV-Analyse Bestimmung des Polygenen Risikoscores (PRS) für Brustkrebs</span></p><p><b>subject</b>: <a href="Patient-mii-exa-molgen-patient-brca1.html">Elisa Schmidt-Huber (official) Female, DoB: 1973-03-12 ( Medical record number (use: usual, ))</a></p><p><b>authoredOn</b>: 2022-11-01</p><p><b>requester</b>: <a href="Practitioner-mii-exa-molgen-practitioner-physician.html">Practitioner Dr. Linda Rubens(official)</a></p><p><b>reasonCode</b>: <span title="Codes:{http://snomed.info/sct 429740004}">Family history of malignant neoplasm of breast (situation)</span>, <span title="Codes:{http://snomed.info/sct 430705002}">Family history of malignant neoplasm of ovary (situation)</span>, <span title="Codes:{http://www.orpha.net 145}">Hereditary breast and/or ovarian cancer syndrome</span>, <span title="Codes:{http://www.omim.org 604370}">BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1; BROVCA1</span></p><p><b>specimen</b>: <a href="Specimen-mii-exa-molgen-specimen-brca1.html">Specimen: identifier = https://www.charite.de/fhir/sid/bioproben#specimen_03; status = available; type = Tissue specimen from breast (specimen); receivedTime = 2022-11-01</a></p></div>
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