MII IG Kerndatensatz-Modul Seltene Erkrankungen
2027.0.0-ballot -
Germany
This page is part of the MII Implementation Guide Seltene Erkrankungen (v2027.0.0-ballot: 2027 Ballot 1) 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
{
"resourceType" : "Observation",
"id" : "mii-exa-seltene-observation-sma-screening",
"language" : "de",
"text" : {
"status" : "generated",
"div" : "<div xml:lang=\"de\" lang=\"de\"><hr/><p><b>German</b></p><hr/><p class=\"res-header-id\"><b>Generated Narrative: Observation mii-exa-seltene-observation-sma-screening</b></p><a name=\"de-mii-exa-seltene-observation-sma-screening\"> </a><a name=\"de-hcmii-exa-seltene-observation-sma-screening\"> </a><p><b>status</b>: Final</p><p><b>category</b>: <span title=\"Codes:{http://terminology.hl7.org/CodeSystem/observation-category laboratory}\">Laboratory</span></p><p><b>code</b>: <span title=\"Codes:{http://loinc.org 92005-8}\">Spinal muscular atrophy newborn screening panel</span></p><p><b>subject</b>: <a href=\"Patient-mii-exa-seltene-patient-sma-001.html\">Anonymous Patient Female, DoB: 2024-07-01 ( https://www.medizininformatik-initiative.de/fhir/sid/patient-id#SMA-2024-001)</a></p><p><b>effective</b>: 2024-07-18</p><p><b>value</b>: <span title=\"Codes:{http://snomed.info/sct 260373001}\">Detected</span></p><p><b>interpretation</b>: <span title=\"Codes:{http://terminology.hl7.org/CodeSystem/v3-ObservationInterpretation A}\">Abnormal</span></p><p><b>note</b>: </p><blockquote><div><p>Positives SMA-Screening. Konfirmatorische Diagnostik empfohlen.</p>\n</div></blockquote><blockquote><p><b>component</b></p><p><b>code</b>: <span title=\"Codes:{http://loinc.org 92004-1}\">Spinal muscular atrophy newborn screen interpretation</span></p><p><b>value</b>: <span title=\"Codes:\">Hinweis auf SMA - SMN1 Exon 7 Deletion nachgewiesen</span></p></blockquote><blockquote><p><b>component</b></p><p><b>code</b>: <span title=\"Codes:{http://loinc.org 92002-5}\">SMN1 gene [Cycle Threshold #] in DBS by NAA with probe detection</span></p><p><b>value</b>: 0 Ct<span style=\"background: LightGoldenRodYellow\"> (Details: UCUM code1 = '1')</span></p><p><b>interpretation</b>: <span title=\"Codes:{http://terminology.hl7.org/CodeSystem/v3-ObservationInterpretation A}\">Abnormal</span></p></blockquote></div>"
},
"status" : "final",
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"code" : "laboratory"
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"code" : {
"coding" : [
{
"system" : "http://loinc.org",
"code" : "92005-8",
"display" : "Spinal muscular atrophy newborn screening panel"
}
]
},
"subject" : {
🔗 "reference" : "Patient/mii-exa-seltene-patient-sma-001"
},
"effectiveDateTime" : "2024-07-18",
"valueCodeableConcept" : {
"coding" : [
{
"system" : "http://snomed.info/sct",
"code" : "260373001",
"display" : "Detected"
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"interpretation" : [
{
"coding" : [
{
"system" : "http://terminology.hl7.org/CodeSystem/v3-ObservationInterpretation",
"code" : "A",
"display" : "Abnormal"
}
]
}
],
"note" : [
{
"text" : "Positives SMA-Screening. Konfirmatorische Diagnostik empfohlen."
}
],
"component" : [
{
"code" : {
"coding" : [
{
"system" : "http://loinc.org",
"code" : "92004-1",
"display" : "Spinal muscular atrophy newborn screen interpretation"
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]
},
"valueCodeableConcept" : {
"text" : "Hinweis auf SMA - SMN1 Exon 7 Deletion nachgewiesen"
}
},
{
"code" : {
"coding" : [
{
"system" : "http://loinc.org",
"code" : "92002-5",
"display" : "SMN1 gene [Cycle Threshold #] in DBS by NAA with probe detection"
}
]
},
"valueQuantity" : {
"value" : 0,
"unit" : "Ct",
"system" : "http://unitsofmeasure.org",
"code" : "1"
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"interpretation" : [
{
"coding" : [
{
"system" : "http://terminology.hl7.org/CodeSystem/v3-ObservationInterpretation",
"code" : "A",
"display" : "Abnormal"
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]
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]
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}