Notice
- Important: This guidance is under active development by NHS England and content may be added or updated on a regular basis.
- This Implementation Guide is currently in Draft and SHOULD NOT be used for development or active implementation without express direction from the NHS England Genomics Unit.
Task-FollowupRecommendationReport-Example
Example of a Task represented a recommneded action to be taken as a consequence of a genomic test, created by a filler organization upon completion of a test, attached to a diagnostic report.
| Task |
| id : Task-FollowupRecommendationReport-Example |
| meta |
| profile : http://hl7.org/fhir/uv/genomics-reporting/StructureDefinition/followup-recommendation |
| status : requested |
| intent : proposal |
| code |
| coding |
| system : http://loinc.org |
| code : LA14021-2 |
| display : Confirmatory testing recommended |
| description : Testing of Pheobe's parents is recommended (via referral to the clinical genetics service) in order to confirm that both are heterozygous carriers of the missense variant. |
| for |
| reference : Patient/Patient-PheobeSmitham-Example |
| reasonReference |
| reference : Observation/Observation-GenomicTherapeuticImplication-Example |
| input |
| type |
| coding |
| system : http://terminology.hl7.org/CodeSystem/v3-RoleCode |
| code : NFTH |
| display : natural father |
| value |
| reference : Patient/Patient-PheobeSmithamFather-Example |
| input |
| type |
| coding |
| system : http://terminology.hl7.org/CodeSystem/v3-RoleCode |
| code : NMTH |
| display : natural mother |
| value |
| reference : Patient/Patient-PheobeSmithamMother-Example |
{
"http://hl7.org/fhir/uv/genomics-reporting/StructureDefinition/followup-recommendation"
]
},
{
}
]
},
"description": "Testing of Pheobe's parents is recommended (via referral to the clinical genetics service) in order to confirm that both are heterozygous carriers of the missense variant.",
},
},
{
{
}
]
},
}
},
{
{
}
]
},
}
}
]
}
<profile value="http://hl7.org/fhir/uv/genomics-reporting/StructureDefinition/followup-recommendation" />
</meta>
</coding>
</code>
<description value="Testing of Pheobe's parents is recommended (via referral to the clinical genetics service) in order to confirm that both are heterozygous carriers of the missense variant." />
</for>
</reasonReference>
</coding>
</type>
</valueReference>
</input>
</coding>
</type>
</valueReference>
</input>
</Task>