FHIR IG analytics| Package | de.medizininformatikinitiative.kerndatensatz.molgen |
| Resource Type | Observation |
| Id | Observation-mii-exa-molgen-diagnostische-implikation-srcc-ctnna1.json |
| FHIR Version | R4 |
No resources found
No resources found
Note: links and images are rebased to the (stated) source
English
Generated Narrative: Observation mii-exa-molgen-diagnostische-implikation-srcc-ctnna1
Profiles: MII PR MolGen Diagnostische Implikation version: 2027.0.0-ballot.1, Diagnostic Implication version: 3.0.0
Related artifact: No display for RelatedArtifact (type: citation; citation: ClinGen; url: https://search.clinicalgenome.org/kb/gene-dosage/HGNC:2509)
status: Final
category: Laboratory, Genetics
code: Diagnostic Implication
subject: Anonymous Patient Male, DoB: 1986-01 ( pseudonymized (use: usual, ))
effective: 2022-11-30
performer: Practitioner Dr. Daniel Schmidt(official)
derivedFrom: Observation Genetic variant assessment
component
code: Conclusion Text
value: Diese Variante wird nach den ACMG/AMP-Kriterien zusammenfasssend als pathogen bewertet entsprechend IARC Class 5.
component
code: Genetic variation clinical significance [Imp]
value: Pathogenic
component
code: Associated phenotype
value: Hereditary diffuse carcinoma of stomach (disorder)
German
Generated Narrative: Observation mii-exa-molgen-diagnostische-implikation-srcc-ctnna1
Profiles: MII PR MolGen Diagnostische Implikation version: 2027.0.0-ballot.1, Diagnostic Implication version: 3.0.0
Related artifact: No display for RelatedArtifact (type: citation; citation: ClinGen; url: https://search.clinicalgenome.org/kb/gene-dosage/HGNC:2509)
status: Final
category: Laboratory, Genetik
code: Diagnostic Implication
subject: Anonymous Patient Male, DoB: 1986-01 ( pseudonymized (use: usual, ))
effective: 2022-11-30
performer: Practitioner Dr. Daniel Schmidt(official)
derivedFrom: Observation Genetic variant assessment
component
code: Conclusion Text
value: Diese Variante wird nach den ACMG/AMP-Kriterien zusammenfasssend als pathogen bewertet entsprechend IARC Class 5.
component
code: Genetic variation clinical significance [Imp]
value: Pathogenic
component
code: Associated phenotype
value: Hereditary diffuse carcinoma of stomach (disorder)
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"text": {
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"div": "<!-- snip (see above) -->"
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"subject": {
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"effectiveDateTime": "2022-11-30",
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"valueString": "Diese Variante wird nach den ACMG/AMP-Kriterien zusammenfasssend als pathogen bewertet entsprechend IARC Class 5."
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