GenomeX Data Exchange FHIR IG
0.2.0 - draft
GenomeX Data Exchange FHIR IG, published by MITRE. This guide is not an authorized publication; it is the continuous build for version 0.2.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/CodeX-HL7-FHIR-Accelerator/GenomeX-DataExchange/ and changes regularly. See the Directory of published versions
{
"resourceType" : "RiskAssessment",
"id" : "PrenatalResidualRiskFamilialHyperinsulinismPatientMale",
"meta" : {
"versionId" : "1",
"lastUpdated" : "2024-09-25T00:01:34.798+00:00",
"source" : "#hrQE3dHjuHuJ5zkf"
},
"text" : {
"status" : "generated",
"div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p class=\"res-header-id\"><b>Generated Narrative: RiskAssessment PrenatalResidualRiskFamilialHyperinsulinismPatientMale</b></p><a name=\"PrenatalResidualRiskFamilialHyperinsulinismPatientMale\"> </a><a name=\"hcPrenatalResidualRiskFamilialHyperinsulinismPatientMale\"> </a><a name=\"PrenatalResidualRiskFamilialHyperinsulinismPatientMale-en-US\"> </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\">version: 1; Last updated: 2024-09-25 00:01:34+0000; </p><p style=\"margin-bottom: 0px\">Information Source: #hrQE3dHjuHuJ5zkf</p></div><p><b>status</b>: Final</p><p><b>subject</b>: <a href=\"Patient-PatientMale.html\">Higado Sobreviviente (official) Male, DoB: 1996-05-13 ( Patient ID: fec6172efdca41b4a13341e75cb62e0f\u00a0(use:\u00a0official,\u00a0))</a></p><p><b>occurrence</b>: 2024-07-09</p><p><b>basis</b>: <a href=\"Observation-PrenatalVariantFamilialHyperinsulinismPatientMale.html\">Observation Genetic variant assessment</a></p><h3>Predictions</h3><table class=\"grid\"><tr><td style=\"display: none\">-</td><td><b>Outcome</b></td><td><b>Probability[x]</b></td></tr><tr><td style=\"display: none\">*</td><td><span title=\"Codes:\">Patient has a disease-causing mutation for familial hyperinsulinism, ABCC8-related</span></td><td>0.00005850664934601126</td></tr></table></div>"
},
"status" : "final",
"subject" : {
🔗 "reference" : "Patient/PatientMale"
},
"occurrenceDateTime" : "2024-07-09",
"basis" : [
{
🔗 "reference" : "Observation/PrenatalVariantFamilialHyperinsulinismPatientMale"
}
],
"prediction" : [
{
"outcome" : {
"text" : "Patient has a disease-causing mutation for familial hyperinsulinism, ABCC8-related"
},
"probabilityDecimal" : 0.00005850664934601126
}
]
}