FHIR IG analytics| Package | fhir.gdx |
| Resource Type | RiskAssessment |
| Id | RiskAssessment-PrenatalResidualRiskAutosomalRecessiveSAoCSPatientMale.json |
| FHIR Version | R4 |
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Note: links and images are rebased to the (stated) source
Generated Narrative: RiskAssessment PrenatalResidualRiskAutosomalRecessiveSAoCSPatientMale
version: 1; Last updated: 2024-09-25 00:01:34+0000;
Information Source: #hrQE3dHjuHuJ5zkf
status: Final
occurrence: 2024-07-09
basis: Observation Genetic variant assessment
| Outcome | Probability[x] |
| Patient has a disease-causing mutation for autosomal recessive spastic ataxia of Charlevoix-Saguenay | 0.00002277238382929289 |
{
"resourceType": "RiskAssessment",
"id": "PrenatalResidualRiskAutosomalRecessiveSAoCSPatientMale",
"meta": {
"versionId": "1",
"lastUpdated": "2024-09-25T00:01:34.798+00:00",
"source": "#hrQE3dHjuHuJ5zkf"
},
"text": {
"status": "generated",
"div": "<!-- snip (see above) -->"
},
"status": "final",
"subject": {
"reference": "Patient/PatientMale"
},
"occurrenceDateTime": "2024-07-09",
"basis": [
{
"reference": "Observation/PrenatalVariantAutosomalRecessiveSAoCSPatientMale"
}
],
"prediction": [
{
"outcome": {
"text": "Patient has a disease-causing mutation for autosomal recessive spastic ataxia of Charlevoix-Saguenay"
},
"probabilityDecimal": 0.00002277238382929289
}
]
}