MII IG Kerndatensatz-Modul Seltene Erkrankungen
2027.0.0-ballot -
Germany
MII IG Kerndatensatz-Modul Seltene Erkrankungen - Downloaded Version 2027.0.0-ballot See the Directory of published versions
{
"resourceType" : "Condition",
"id" : "mii-exa-seltene-example-dmd-genetic-diagnosis",
"meta" : {
"profile" : [
🔗 "https://www.medizininformatik-initiative.de/fhir/ext/modul-seltene/StructureDefinition/mii-pr-seltene-genetic-diagnosis|2027.0.0-ballot"
]
},
"language" : "de",
"text" : {
"status" : "extensions",
"div" : "<div xml:lang=\"de\" lang=\"de\"><hr/><p><b>German</b></p><hr/><p class=\"res-header-id\"><b>Generated Narrative: Condition mii-exa-seltene-example-dmd-genetic-diagnosis</b></p><a name=\"de-mii-exa-seltene-example-dmd-genetic-diagnosis\"> </a><a name=\"de-hcmii-exa-seltene-example-dmd-genetic-diagnosis\"> </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-seltene-genetic-diagnosis.html\">MII PR SE Genetic Diagnosis</a> version: 2027.0.0-ballot</p></div><p><b>Condition Asserted Date</b>: 2024-09-15</p><p><b>clinicalStatus</b>: <span title=\"Codes:{http://terminology.hl7.org/CodeSystem/condition-clinical active}\">Active</span></p><p><b>verificationStatus</b>: <span title=\"Codes:{http://terminology.hl7.org/CodeSystem/condition-ver-status confirmed}\">Confirmed</span></p><p><b>category</b>: <span title=\"Codes:{http://snomed.info/sct 782964007}\">Genetic disease</span></p><p><b>code</b>: <span title=\"Codes:{http://omim.org 310200}, {http://snomed.info/sct 76670001}, {http://www.orpha.net 98896}\">Duchenne-Muskeldystrophie</span></p><p><b>subject</b>: <a href=\"Patient-mii-exa-seltene-patient.html\">Max Mustermann (official) Male, DoB: 1990-01-01 ( http://test-krankenhaus.de/fhir/sid/patienten#12345)</a></p><p><b>recordedDate</b>: 2024-09-15</p><blockquote><p><b>evidence</b></p><p><b>code</b>: <span title=\"Codes:{http://snomed.info/sct 106221001}\">Genetic finding</span></p><p><b>detail</b>: <a href=\"Observation-mii-exa-seltene-molgen-variant-dmd-deletion-exon45.html\">Observation Genetic variant assessment</a></p></blockquote><blockquote><p><b>evidence</b></p><p><b>code</b>: <span title=\"Codes:{http://snomed.info/sct 405824009}\">Genetic test</span></p><p><b>detail</b>: <a href=\"DiagnosticReport-mii-exa-seltene-molgen-diagnostic-dmd-duchenne.html\">Diagnostic Report for 'Genetic analysis report' for '->Max Mustermann (official) Male, DoB: 1990-01-01 ( http://test-krankenhaus.de/fhir/sid/patienten#12345)'</a></p></blockquote><p><b>note</b>: </p><blockquote><div><p>Deletion des Exons 45 im DMD-Gen nachgewiesen. Out-of-frame Deletion mit Leserasterverschiebung, kein funktionsfaehiges Dystrophin. (Bis 2026-09-03 stand hier die Deletion der Exons 45-47 — die ist in-frame und fuehrt zu Becker, nicht zu Duchenne.)</p>\n</div></blockquote></div>"
},
"extension" : [
{
"url" : "http://hl7.org/fhir/StructureDefinition/condition-assertedDate",
"valueDateTime" : "2024-09-15"
}
],
"clinicalStatus" : {
"coding" : [
{
"system" : "http://terminology.hl7.org/CodeSystem/condition-clinical",
"code" : "active"
}
]
},
"verificationStatus" : {
"coding" : [
{
"system" : "http://terminology.hl7.org/CodeSystem/condition-ver-status",
"code" : "confirmed"
}
]
},
"category" : [
{
"coding" : [
{
"system" : "http://snomed.info/sct",
"code" : "782964007",
"display" : "Genetic disease"
}
]
}
],
"code" : {
"coding" : [
{
"system" : "http://omim.org",
"version" : "2024",
"code" : "310200",
"display" : "Duchenne muscular dystrophy"
},
{
"system" : "http://snomed.info/sct",
"code" : "76670001",
"display" : "Duchenne muscular dystrophy"
},
{
"system" : "http://www.orpha.net",
"code" : "98896",
"display" : "Duchenne muscular dystrophy"
}
],
"text" : "Duchenne-Muskeldystrophie"
},
"subject" : {
🔗 "reference" : "Patient/mii-exa-seltene-patient"
},
"recordedDate" : "2024-09-15",
"evidence" : [
{
"code" : [
{
"coding" : [
{
"system" : "http://snomed.info/sct",
"code" : "106221001",
"display" : "Genetic finding"
}
]
}
],
"detail" : [
{
🔗 "reference" : "Observation/mii-exa-seltene-molgen-variant-dmd-deletion-exon45"
}
]
},
{
"code" : [
{
"coding" : [
{
"system" : "http://snomed.info/sct",
"code" : "405824009",
"display" : "Genetic test"
}
]
}
],
"detail" : [
{
🔗 "reference" : "DiagnosticReport/mii-exa-seltene-molgen-diagnostic-dmd-duchenne"
}
]
}
],
"note" : [
{
"text" : "Deletion des Exons 45 im DMD-Gen nachgewiesen. Out-of-frame Deletion mit Leserasterverschiebung, kein funktionsfaehiges Dystrophin. (Bis 2026-09-03 stand hier die Deletion der Exons 45-47 — die ist in-frame und fuehrt zu Becker, nicht zu Duchenne.)"
}
]
}