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.
ServiceRequest-SavedTestOrderWGS-Example
Example of a ServiceRequest. After being saved on the central broker, the ServiceRequest is assigned a unique identifier.
ServiceRequest |
id : ServiceRequest-SavedTestOrderWGS-Example |
extension |
url : https://fhir.hl7.org.uk/StructureDefinition/Extension-UKCore-Coverage |
value |
coding |
system : https://fhir.hl7.org.uk/CodeSystem/UKCore-FundingCategory |
code : nhs-england |
display : NHS England |
identifier |
system : https://fhir.nhs.uk/Id/GMSOrder |
value : RAS61763 |
status : active |
intent : order |
category |
coding |
system : https://fhir.hl7.org.uk/CodeSystem/UKCore-GenomeSequencingCategory |
code : rare-disease-wgs |
display : Rare Disease - WGS |
category |
coding |
system : https://fhir.nhs.uk/CodeSystem/reasonfortesting-genomics |
code : diagnostic |
display : Diagnostic |
priority : routine |
code |
coding |
system : https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectory |
code : R193.4 |
display : Cystic renal disease |
version : 7 |
subject |
reference : Patient/Patient-LindsaySorrell-Example |
identifier |
system : https://fhir.nhs.uk/Id/nhs-number |
value : 9449307946 |
authoredOn : 2023-08-08 |
requester |
reference : PractitionerRole/PractitionerRole-HazelSmithRenal-Example |
supportingInfo |
reference : Observation/Observation-GenomicEthnicity-Example |
supportingInfo |
reference : Condition/Condition-MonogenicHearingLoss-Example |
supportingInfo |
reference : Observation/Observation-NoPregnancy-Example |
supportingInfo |
reference : Observation/Observation-NoBoneMarrowTransplant-Example |
supportingInfo |
reference : Observation/Observation-NoTransfusion-Example |
supportingInfo |
reference : Observation/Observation-MultipleRenalCysts-Example |
supportingInfo |
reference : Observation/Observation-Nephronophthisis-Example |
supportingInfo |
reference : Observation/Observation-HepaticCysts-Example |
supportingInfo |
reference : Observation/Observation-EnlargedKidney-Example |
supportingInfo |
reference : Observation/Observation-RenalInsufficiency-Example |
supportingInfo |
reference : Consent/Consent-RoDToFollow-Example |
note |
text : No family history of genomic testing |
note |
text : Free text for diagnosis/reason for referral, relevant information including family history, phenotypic details/ HPO Terms/ Patient diagnoses with ADPKD (example) |
{
{
{
}
]
}
}
],
],
{
{
}
]
},
{
{
}
]
}
],
{
}
]
},
}
},
},
{
},
{
},
{
},
{
},
{
},
{
},
{
},
{
},
{
},
{
},
{
}
],
{
},
{
"text": "Free text for diagnosis/reason for referral, relevant information including family history, phenotypic details/ HPO Terms/ Patient diagnoses with ADPKD (example)"
}
]
}
</coding>
</valueCodeableConcept>
</extension>
</identifier>
</coding>
</category>
</coding>
</category>
</coding>
</code>
</identifier>
</subject>
</requester>
</supportingInfo>
</supportingInfo>
</supportingInfo>
</supportingInfo>
</supportingInfo>
</supportingInfo>
</supportingInfo>
</supportingInfo>
</supportingInfo>
</supportingInfo>
</supportingInfo>
</note>
<text value="Free text for diagnosis/reason for referral, relevant information including family history, phenotypic details/ HPO Terms/ Patient diagnoses with ADPKD (example)" />
</note>
</ServiceRequest>