diff --git a/Bundle/Bundle-NonWGSScenario3-FetusAsProband-Example.json b/Bundle/Bundle-NonWGSScenario3-FetusAsProband-Example.json index 2c05f8ba..344d4eba 100644 --- a/Bundle/Bundle-NonWGSScenario3-FetusAsProband-Example.json +++ b/Bundle/Bundle-NonWGSScenario3-FetusAsProband-Example.json @@ -180,7 +180,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT1133", "display": "Common aneuploidy testing", "extension": [ @@ -213,7 +213,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP289", "display": "Common aneuploidy testing - prenatal", "extension": [ @@ -405,7 +405,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT1133", "display": "Common aneuploidy testing", "extension": [ @@ -432,7 +432,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP289", "display": "Common aneuploidy testing - prenatal", "extension": [ diff --git a/Bundle/Bundle-NonWGSScenario4-ProbandWithMultipleFetus-Example.json b/Bundle/Bundle-NonWGSScenario4-ProbandWithMultipleFetus-Example.json index fd8d963a..dee47b09 100644 --- a/Bundle/Bundle-NonWGSScenario4-ProbandWithMultipleFetus-Example.json +++ b/Bundle/Bundle-NonWGSScenario4-ProbandWithMultipleFetus-Example.json @@ -181,7 +181,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT1133", "display": "Common aneuploidy testing", "extension": [ @@ -214,7 +214,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP289", "display": "Common aneuploidy testing - prenatal", "extension": [ @@ -491,7 +491,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT1133", "display": "Common aneuploidy testing", "extension": [ @@ -524,7 +524,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP289", "display": "Common aneuploidy testing - prenatal", "extension": [ @@ -757,7 +757,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT1133", "display": "Common aneuploidy testing", "extension": [ @@ -784,7 +784,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP289", "display": "Common aneuploidy testing - prenatal", "extension": [ @@ -906,7 +906,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT1133", "display": "Common aneuploidy testing", "extension": [ @@ -933,7 +933,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP289", "display": "Common aneuploidy testing - prenatal", "extension": [ diff --git a/Bundle/Bundle-NonWGSScenario5-ProductsofConception-Example.json b/Bundle/Bundle-NonWGSScenario5-ProductsofConception-Example.json index a8c2ee7f..b9b0b9b5 100644 --- a/Bundle/Bundle-NonWGSScenario5-ProductsofConception-Example.json +++ b/Bundle/Bundle-NonWGSScenario5-ProductsofConception-Example.json @@ -293,7 +293,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT1133", "display": "Common aneuploidy testing", "extension": [ @@ -326,7 +326,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP289", "display": "Common aneuploidy testing - prenatal", "extension": [ diff --git a/Bundle/Bundle-NonWGSTestOrderForm-CancerSolidTumor-Example.json b/Bundle/Bundle-NonWGSTestOrderForm-CancerSolidTumor-Example.json index ec0158be..d8258790 100644 --- a/Bundle/Bundle-NonWGSTestOrderForm-CancerSolidTumor-Example.json +++ b/Bundle/Bundle-NonWGSTestOrderForm-CancerSolidTumor-Example.json @@ -515,7 +515,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT1046", "display": "Paediatric Tumour Differential Diagnosis - NGS Panel SNV and CNV", "extension": [ @@ -542,7 +542,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP550", "display": "Paediatric Tumours", "extension": [ diff --git a/Bundle/Bundle-NonWGSTestOrderForm-Example.json b/Bundle/Bundle-NonWGSTestOrderForm-Example.json index 62153b90..76010312 100644 --- a/Bundle/Bundle-NonWGSTestOrderForm-Example.json +++ b/Bundle/Bundle-NonWGSTestOrderForm-Example.json @@ -238,7 +238,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT488", "display": "Monogenic hearing loss - Panel sequencing", "extension": [ @@ -265,7 +265,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP439", "display": "Monogenic hearing loss", "extension": [ @@ -367,7 +367,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP439", "display": "Monogenic hearing loss" } diff --git a/Bundle/Bundle-NonWGSTestOrderForm-FetalScenario-Example.json b/Bundle/Bundle-NonWGSTestOrderForm-FetalScenario-Example.json index c228d35f..614ff995 100644 --- a/Bundle/Bundle-NonWGSTestOrderForm-FetalScenario-Example.json +++ b/Bundle/Bundle-NonWGSTestOrderForm-FetalScenario-Example.json @@ -371,7 +371,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP289", "display": "Common aneuploidy testing - prenatal", "extension": [ @@ -473,7 +473,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP289", "display": "Common aneuploidy testing - prenatal", "extension": [ @@ -602,7 +602,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP289", "display": "Common aneuploidy testing - prenatal", "extension": [ diff --git a/Bundle/Bundle-NonWGSTestOrderForm-Reanalysis-Example.json b/Bundle/Bundle-NonWGSTestOrderForm-Reanalysis-Example.json index 44e246ac..5be8ccb3 100644 --- a/Bundle/Bundle-NonWGSTestOrderForm-Reanalysis-Example.json +++ b/Bundle/Bundle-NonWGSTestOrderForm-Reanalysis-Example.json @@ -253,7 +253,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT192", "display": "Reanalysis of existing data", "extension": [ @@ -280,7 +280,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP459", "display": "Paediatric disorders", "extension": [ @@ -387,7 +387,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP439", "display": "Monogenic hearing loss" } diff --git a/Bundle/Bundle-NonWGSTestOrderFormQRPatientExtensions-Example.json b/Bundle/Bundle-NonWGSTestOrderFormQRPatientExtensions-Example.json index 53499f61..e28eaf0a 100644 --- a/Bundle/Bundle-NonWGSTestOrderFormQRPatientExtensions-Example.json +++ b/Bundle/Bundle-NonWGSTestOrderFormQRPatientExtensions-Example.json @@ -171,7 +171,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT488", "display": "Monogenic hearing loss - Panel sequencing", "extension": [ @@ -197,7 +197,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP439", "display": "Monogenic hearing loss", "extension": [ @@ -301,7 +301,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP439", "display": "Monogenic hearing loss" } diff --git a/Bundle/Bundle-NonWGSTestOrderFormUpdated-FetalScenario-Example.json b/Bundle/Bundle-NonWGSTestOrderFormUpdated-FetalScenario-Example.json index a3a70c81..b63c05ea 100644 --- a/Bundle/Bundle-NonWGSTestOrderFormUpdated-FetalScenario-Example.json +++ b/Bundle/Bundle-NonWGSTestOrderFormUpdated-FetalScenario-Example.json @@ -79,7 +79,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP289", "display": "Common aneuploidy testing - prenatal", "extension": [ diff --git a/Bundle/Bundle-TransactionResponseSuccess-Example.json b/Bundle/Bundle-TransactionResponseSuccess-Example.json index edb75f6a..1b3102bf 100644 --- a/Bundle/Bundle-TransactionResponseSuccess-Example.json +++ b/Bundle/Bundle-TransactionResponseSuccess-Example.json @@ -42,7 +42,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT488", "display": "Monogenic hearing loss - Panel sequencing", "extension": [ @@ -69,7 +69,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP439", "display": "Monogenic hearing loss", "extension": [ diff --git a/Bundle/Bundle-WGSTestOrderForm-Example.json b/Bundle/Bundle-WGSTestOrderForm-Example.json index eebf7502..736d1dc4 100644 --- a/Bundle/Bundle-WGSTestOrderForm-Example.json +++ b/Bundle/Bundle-WGSTestOrderForm-Example.json @@ -236,7 +236,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT497", "display": "Cystic renal disease - WGS", "extension": [ @@ -263,7 +263,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP171", "display": "Cystic renal disease", "extension": [ @@ -380,7 +380,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP439", "display": "Monogenic hearing loss" } diff --git a/Bundle/CommunityCloud-Bundle-Example.json b/Bundle/CommunityCloud-Bundle-Example.json index 56ff7992..a30d8b07 100644 --- a/Bundle/CommunityCloud-Bundle-Example.json +++ b/Bundle/CommunityCloud-Bundle-Example.json @@ -298,7 +298,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP442", "display": "Familial hypercholesterolaemia" } diff --git a/Condition/Condition-MonogenicHearingLoss-Example.json b/Condition/Condition-MonogenicHearingLoss-Example.json index fdf5de6d..a303a0e3 100644 --- a/Condition/Condition-MonogenicHearingLoss-Example.json +++ b/Condition/Condition-MonogenicHearingLoss-Example.json @@ -22,7 +22,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP439", "display": "Monogenic hearing loss" } diff --git a/Observation/Observation-DiseasePenetrance-Example.json b/Observation/Observation-DiseasePenetrance-Example.json index 0c40c380..29923501 100644 --- a/Observation/Observation-DiseasePenetrance-Example.json +++ b/Observation/Observation-DiseasePenetrance-Example.json @@ -31,7 +31,7 @@ "valueCodeableConcept": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP12", "display": "Acutely unwell children with a likely monogenic disorder" } diff --git a/Observation/Observation-DiseasePenetrancePheobeSmitham-Example.json b/Observation/Observation-DiseasePenetrancePheobeSmitham-Example.json index 884173a1..539f6952 100644 --- a/Observation/Observation-DiseasePenetrancePheobeSmitham-Example.json +++ b/Observation/Observation-DiseasePenetrancePheobeSmitham-Example.json @@ -31,7 +31,7 @@ "valueCodeableConcept": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP12", "display": "Acutely unwell children with a likely monogenic disorder" } diff --git a/Observation/Observation-NatureAndAgeOfHearingLoss-Example.json b/Observation/Observation-NatureAndAgeOfHearingLoss-Example.json index 3c5056cb..0d54d781 100644 --- a/Observation/Observation-NatureAndAgeOfHearingLoss-Example.json +++ b/Observation/Observation-NatureAndAgeOfHearingLoss-Example.json @@ -14,7 +14,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP439", "display": "Monogenic hearing loss" } diff --git a/Patient/Patient-LindsaySorrellNHSNumberUnavailable-Example.json b/Patient/Patient-LindsaySorrellNHSNumberUnavailable-Example.json index 4091bedb..ec7739d6 100644 --- a/Patient/Patient-LindsaySorrellNHSNumberUnavailable-Example.json +++ b/Patient/Patient-LindsaySorrellNHSNumberUnavailable-Example.json @@ -85,13 +85,5 @@ }, "display": "anywhere place" } - ], - "link": [ - { - "other": { - "reference": "https://api.service.nhs.uk/personal-demographics/FHIR/R4/Patient/9449307946" - }, - "type": "seealso" - } ] } \ No newline at end of file diff --git a/Procedure/CommunityCloud-GenomicStudy-Example.json b/Procedure/CommunityCloud-GenomicStudy-Example.json index 12a81104..009659d3 100644 --- a/Procedure/CommunityCloud-GenomicStudy-Example.json +++ b/Procedure/CommunityCloud-GenomicStudy-Example.json @@ -37,7 +37,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP442", "display": "Familial hypercholesterolaemia" } diff --git a/ServiceRequest/ServiceRequest-NonWGSTestOrder-VariantReinterpretation-Example.json b/ServiceRequest/ServiceRequest-NonWGSTestOrder-VariantReinterpretation-Example.json index 33a1b6f3..43ae8767 100644 --- a/ServiceRequest/ServiceRequest-NonWGSTestOrder-VariantReinterpretation-Example.json +++ b/ServiceRequest/ServiceRequest-NonWGSTestOrder-VariantReinterpretation-Example.json @@ -37,7 +37,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT1013", "display": "Variant Re-interpretation", "extension": [ @@ -75,7 +75,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP459", "display": "Paediatric disorders", "extension": [ diff --git a/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-Cancellation-Example.json b/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-Cancellation-Example.json index 02a181d8..f4768bd3 100644 --- a/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-Cancellation-Example.json +++ b/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-Cancellation-Example.json @@ -32,7 +32,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT488", "display": "Monogenic hearing loss - Panel sequencing", "extension": [ @@ -59,7 +59,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP439", "display": "Monogenic hearing loss", "extension": [ diff --git a/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-CancerSolidTumor-Example.json b/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-CancerSolidTumor-Example.json index bb720105..2182d3c4 100644 --- a/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-CancerSolidTumor-Example.json +++ b/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-CancerSolidTumor-Example.json @@ -38,7 +38,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT1046", "display": "Paediatric Tumour Differential Diagnosis - NGS Panel SNV and CNV", "extension": [ @@ -65,7 +65,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP550", "display": "Paediatric Tumours", "extension": [ diff --git a/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-CascadeTesting-Example.json b/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-CascadeTesting-Example.json index c3545870..934a12b9 100644 --- a/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-CascadeTesting-Example.json +++ b/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-CascadeTesting-Example.json @@ -49,7 +49,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP442", "display": "Familial hypercholesterolaemia", "extension": [ diff --git a/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-DeceasedPatient-Example.json b/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-DeceasedPatient-Example.json index 1e686b75..fc66b1c8 100644 --- a/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-DeceasedPatient-Example.json +++ b/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-DeceasedPatient-Example.json @@ -44,7 +44,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP119", "display": "Sudden unexplained death or survivors of a cardiac event", "extension": [ diff --git a/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-Example.json b/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-Example.json index 6c7602df..7de5e6f2 100644 --- a/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-Example.json +++ b/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-Example.json @@ -32,7 +32,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT488", "display": "Monogenic hearing loss - Panel sequencing", "extension": [ @@ -59,7 +59,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP439", "display": "Monogenic hearing loss", "extension": [ diff --git a/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-FetalScenario-Example.json b/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-FetalScenario-Example.json index 8ca7d196..917ed01b 100644 --- a/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-FetalScenario-Example.json +++ b/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-FetalScenario-Example.json @@ -76,7 +76,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP289", "display": "Common aneuploidy testing - prenatal", "extension": [ diff --git a/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-FetalScenarioFather-Example.json b/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-FetalScenarioFather-Example.json index 8a54a833..df055f9e 100644 --- a/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-FetalScenarioFather-Example.json +++ b/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-FetalScenarioFather-Example.json @@ -76,7 +76,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP289", "display": "Common aneuploidy testing - prenatal", "extension": [ diff --git a/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-FollowupTest-Example.json b/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-FollowupTest-Example.json index ff824728..5b0556d7 100644 --- a/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-FollowupTest-Example.json +++ b/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-FollowupTest-Example.json @@ -44,7 +44,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP46", "display": "Cystic fibrosis - Diagnostic", "extension": [ diff --git a/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-HaemOncology-Example.json b/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-HaemOncology-Example.json index 5bf0237f..417d8703 100644 --- a/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-HaemOncology-Example.json +++ b/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-HaemOncology-Example.json @@ -44,7 +44,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP34", "display": "Acute Lymphoblastic Leukaemia - T cell", "extension": [ diff --git a/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-HaemOncologyUpdated-Example.json b/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-HaemOncologyUpdated-Example.json index 8e98f99c..b4a0aa86 100644 --- a/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-HaemOncologyUpdated-Example.json +++ b/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-HaemOncologyUpdated-Example.json @@ -36,7 +36,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT200", "display": "Other FISH Targets - ALL", "extension": [ @@ -63,7 +63,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP34", "display": "Acute Lymphoblastic Leukaemia - T cell", "extension": [ diff --git a/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-NewFollowupTest-Example.json b/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-NewFollowupTest-Example.json index c007a4fc..9451a0c5 100644 --- a/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-NewFollowupTest-Example.json +++ b/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-NewFollowupTest-Example.json @@ -37,7 +37,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT645", "display": "MT-RNR1 - Targeted variant testing", "extension": [ @@ -65,7 +65,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP154", "display": "Aminoglycoside exposure posing risk to hearing", "extension": [ diff --git a/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-OutOfCountry-Example.json b/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-OutOfCountry-Example.json index c55a914a..10000a55 100644 --- a/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-OutOfCountry-Example.json +++ b/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-OutOfCountry-Example.json @@ -38,7 +38,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT1272", "display": "ETV6::NTRK3 targeted assay", "extension": [ @@ -65,7 +65,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP580", "display": "Breast Cancer", "extension": [ diff --git a/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-ReAnalysis-Example.json b/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-ReAnalysis-Example.json index 559b1560..ca4e41ae 100644 --- a/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-ReAnalysis-Example.json +++ b/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-ReAnalysis-Example.json @@ -38,7 +38,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT192", "display": "Reanalysis of existing data", "extension": [ @@ -65,7 +65,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP459", "display": "Paediatric disorders", "extension": [ diff --git a/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-UsingStoredSample-Example.json b/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-UsingStoredSample-Example.json index 82c3b6ad..81385eb6 100644 --- a/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-UsingStoredSample-Example.json +++ b/ServiceRequest/ServiceRequest-NonWGSTestOrderForm-UsingStoredSample-Example.json @@ -44,7 +44,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP442", "display": "Familial hypercholesterolaemia", "extension": [ diff --git a/ServiceRequest/ServiceRequest-NonWGSTestOrderFormUpdated-Cancellation-Example.json b/ServiceRequest/ServiceRequest-NonWGSTestOrderFormUpdated-Cancellation-Example.json index cca064ee..d5a37429 100644 --- a/ServiceRequest/ServiceRequest-NonWGSTestOrderFormUpdated-Cancellation-Example.json +++ b/ServiceRequest/ServiceRequest-NonWGSTestOrderFormUpdated-Cancellation-Example.json @@ -36,7 +36,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT488", "display": "Monogenic hearing loss - Panel sequencing", "extension": [ @@ -63,7 +63,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP439", "display": "Monogenic hearing loss", "extension": [ diff --git a/ServiceRequest/ServiceRequest-NonWGSTestOrderFormUpdated-SolidTumor-Example.json b/ServiceRequest/ServiceRequest-NonWGSTestOrderFormUpdated-SolidTumor-Example.json index cb2bbf1c..20a1fe38 100644 --- a/ServiceRequest/ServiceRequest-NonWGSTestOrderFormUpdated-SolidTumor-Example.json +++ b/ServiceRequest/ServiceRequest-NonWGSTestOrderFormUpdated-SolidTumor-Example.json @@ -42,7 +42,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT1046", "display": "Paediatric Tumour Differential Diagnosis - NGS Panel SNV and CNV", "extension": [ @@ -69,7 +69,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP550", "display": "Paediatric Tumours", "extension": [ diff --git a/ServiceRequest/ServiceRequest-SavedTestOrder-Example.json b/ServiceRequest/ServiceRequest-SavedTestOrder-Example.json index 52ed1fd8..02d1dacf 100644 --- a/ServiceRequest/ServiceRequest-SavedTestOrder-Example.json +++ b/ServiceRequest/ServiceRequest-SavedTestOrder-Example.json @@ -38,7 +38,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT488", "display": "Monogenic hearing loss - Panel sequencing", "extension": [ @@ -65,7 +65,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP439", "display": "Monogenic hearing loss", "extension": [ diff --git a/ServiceRequest/ServiceRequest-SavedTestOrderUpdated-CascadeTesting-Example.json b/ServiceRequest/ServiceRequest-SavedTestOrderUpdated-CascadeTesting-Example.json index 741806b5..5d492cf4 100644 --- a/ServiceRequest/ServiceRequest-SavedTestOrderUpdated-CascadeTesting-Example.json +++ b/ServiceRequest/ServiceRequest-SavedTestOrderUpdated-CascadeTesting-Example.json @@ -41,7 +41,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT36", "display": "Predictive testing for known variant(s) - Targeted variant testing", "extension": [ @@ -68,7 +68,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP442", "display": "Familial hypercholesterolaemia", "extension": [ diff --git a/ServiceRequest/ServiceRequest-SavedTestOrderUpdated-Example.json b/ServiceRequest/ServiceRequest-SavedTestOrderUpdated-Example.json index 26e18f63..689e9062 100644 --- a/ServiceRequest/ServiceRequest-SavedTestOrderUpdated-Example.json +++ b/ServiceRequest/ServiceRequest-SavedTestOrderUpdated-Example.json @@ -42,7 +42,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT488", "display": "Monogenic hearing loss - Panel sequencing", "extension": [ @@ -73,7 +73,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP439", "display": "Monogenic hearing loss", "extension": [ diff --git a/ServiceRequest/ServiceRequest-SavedTestOrderWGS-Example.json b/ServiceRequest/ServiceRequest-SavedTestOrderWGS-Example.json index 9302f041..f42bf75f 100644 --- a/ServiceRequest/ServiceRequest-SavedTestOrderWGS-Example.json +++ b/ServiceRequest/ServiceRequest-SavedTestOrderWGS-Example.json @@ -38,7 +38,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT497", "display": "Cystic renal disease - WGS", "extension": [ @@ -65,7 +65,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP171", "display": "Cystic renal disease", "extension": [ diff --git a/ServiceRequest/ServiceRequest-TestOrderForm-StorageOfMaterial-Example.json b/ServiceRequest/ServiceRequest-TestOrderForm-StorageOfMaterial-Example.json index a7f519a2..d5541ddc 100644 --- a/ServiceRequest/ServiceRequest-TestOrderForm-StorageOfMaterial-Example.json +++ b/ServiceRequest/ServiceRequest-TestOrderForm-StorageOfMaterial-Example.json @@ -32,7 +32,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT905", "display": "DNA extraction and storage", "extension": [ @@ -59,7 +59,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP347", "display": "Sample Storage", "extension": [ diff --git a/ServiceRequest/ServiceRequest-WGSTestOrderForm-CancerHaemOnc-Example.json b/ServiceRequest/ServiceRequest-WGSTestOrderForm-CancerHaemOnc-Example.json index 4c30f628..d6f58057 100644 --- a/ServiceRequest/ServiceRequest-WGSTestOrderForm-CancerHaemOnc-Example.json +++ b/ServiceRequest/ServiceRequest-WGSTestOrderForm-CancerHaemOnc-Example.json @@ -38,7 +38,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT254", "display": "WGS Tumour First - Acute leukaemia other", "extension": [ @@ -65,7 +65,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP34", "display": "Acute Lymphoblastic Leukaemia - T cell", "extension": [ diff --git a/ServiceRequest/ServiceRequest-WGSTestOrderForm-CancerSolidTumor-Example.json b/ServiceRequest/ServiceRequest-WGSTestOrderForm-CancerSolidTumor-Example.json index 433450a8..f98a8bea 100644 --- a/ServiceRequest/ServiceRequest-WGSTestOrderForm-CancerSolidTumor-Example.json +++ b/ServiceRequest/ServiceRequest-WGSTestOrderForm-CancerSolidTumor-Example.json @@ -38,7 +38,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT469", "display": "High Grade Ovarian Carcinoma WGS", "extension": [ @@ -65,7 +65,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP589", "display": "Ovarian Carcinoma - Merged", "extension": [ diff --git a/ServiceRequest/ServiceRequest-WGSTestOrderForm-DirectToLab-Example.json b/ServiceRequest/ServiceRequest-WGSTestOrderForm-DirectToLab-Example.json index 362b4d0e..8788c46d 100644 --- a/ServiceRequest/ServiceRequest-WGSTestOrderForm-DirectToLab-Example.json +++ b/ServiceRequest/ServiceRequest-WGSTestOrderForm-DirectToLab-Example.json @@ -44,7 +44,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP12", "display": "Acutely unwell children with a likely monogenic disorder", "extension": [ diff --git a/ServiceRequest/ServiceRequest-WGSTestOrderForm-Example.json b/ServiceRequest/ServiceRequest-WGSTestOrderForm-Example.json index b8648bc9..e80448bd 100644 --- a/ServiceRequest/ServiceRequest-WGSTestOrderForm-Example.json +++ b/ServiceRequest/ServiceRequest-WGSTestOrderForm-Example.json @@ -32,7 +32,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT497", "display": "Cystic renal disease - WGS", "extension": [ @@ -59,7 +59,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP171", "display": "Cystic renal disease", "extension": [ diff --git a/ServiceRequest/ServiceRequest-WGSTestOrderForm-GermlineLate-Example.json b/ServiceRequest/ServiceRequest-WGSTestOrderForm-GermlineLate-Example.json index 7cd83bf8..8e486fa6 100644 --- a/ServiceRequest/ServiceRequest-WGSTestOrderForm-GermlineLate-Example.json +++ b/ServiceRequest/ServiceRequest-WGSTestOrderForm-GermlineLate-Example.json @@ -43,7 +43,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT825", "display": "WGS Follow-up Germline - Acute Leukaemia Other", "extension": [ @@ -70,7 +70,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP34", "display": "Acute Lymphoblastic Leukaemia - T cell", "extension": [ diff --git a/ServiceRequest/ServiceRequest-WGSTestOrderForm-TrioTestingProband-Example.json b/ServiceRequest/ServiceRequest-WGSTestOrderForm-TrioTestingProband-Example.json index 526c05d2..45e115f8 100644 --- a/ServiceRequest/ServiceRequest-WGSTestOrderForm-TrioTestingProband-Example.json +++ b/ServiceRequest/ServiceRequest-WGSTestOrderForm-TrioTestingProband-Example.json @@ -64,7 +64,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT317", "display": "Likely inborn error of metabolism - WGS", "extension": [ @@ -92,7 +92,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP229", "display": "Likely inborn error of metabolism", "extension": [ diff --git a/ServiceRequest/ServiceRequest-WGSTestOrderForm-TrioTestingProbandDGTS-Example.json b/ServiceRequest/ServiceRequest-WGSTestOrderForm-TrioTestingProbandDGTS-Example.json index 709c208c..18d84bde 100644 --- a/ServiceRequest/ServiceRequest-WGSTestOrderForm-TrioTestingProbandDGTS-Example.json +++ b/ServiceRequest/ServiceRequest-WGSTestOrderForm-TrioTestingProbandDGTS-Example.json @@ -64,7 +64,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT317", "display": "Likely inborn error of metabolism - WGS", "extension": [ @@ -92,7 +92,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP229", "display": "Likely inborn error of metabolism", "extension": [ diff --git a/ServiceRequest/ServiceRequest-WGSTestOrderForm-TrioTestingProbandFather-Example.json b/ServiceRequest/ServiceRequest-WGSTestOrderForm-TrioTestingProbandFather-Example.json index 74545564..e5ec7a65 100644 --- a/ServiceRequest/ServiceRequest-WGSTestOrderForm-TrioTestingProbandFather-Example.json +++ b/ServiceRequest/ServiceRequest-WGSTestOrderForm-TrioTestingProbandFather-Example.json @@ -60,7 +60,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT317", "display": "Likely inborn error of metabolism - WGS", "extension": [ @@ -88,7 +88,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP229", "display": "Likely inborn error of metabolism", "extension": [ diff --git a/ServiceRequest/ServiceRequest-WGSTestOrderForm-TrioTestingProbandMother-Example.json b/ServiceRequest/ServiceRequest-WGSTestOrderForm-TrioTestingProbandMother-Example.json index 77a909fd..0ee24975 100644 --- a/ServiceRequest/ServiceRequest-WGSTestOrderForm-TrioTestingProbandMother-Example.json +++ b/ServiceRequest/ServiceRequest-WGSTestOrderForm-TrioTestingProbandMother-Example.json @@ -60,7 +60,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT317", "display": "Likely inborn error of metabolism - WGS", "extension": [ @@ -88,7 +88,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP229", "display": "Likely inborn error of metabolism", "extension": [ diff --git a/ServiceRequest/ServiceRequest-WGSTestOrderFormUpdated-DirectToLab-Example.json b/ServiceRequest/ServiceRequest-WGSTestOrderFormUpdated-DirectToLab-Example.json index b077a7c0..43e53522 100644 --- a/ServiceRequest/ServiceRequest-WGSTestOrderFormUpdated-DirectToLab-Example.json +++ b/ServiceRequest/ServiceRequest-WGSTestOrderFormUpdated-DirectToLab-Example.json @@ -48,7 +48,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP12", "display": "Acutely unwell children with a likely monogenic disorder", "extension": [ diff --git a/ServiceRequest/ServiceRequest-WGSTestOrderFormUpdated-TrioTesting-Example.json b/ServiceRequest/ServiceRequest-WGSTestOrderFormUpdated-TrioTesting-Example.json index 6c52fb10..45ef028c 100644 --- a/ServiceRequest/ServiceRequest-WGSTestOrderFormUpdated-TrioTesting-Example.json +++ b/ServiceRequest/ServiceRequest-WGSTestOrderFormUpdated-TrioTesting-Example.json @@ -72,7 +72,7 @@ "code": { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "GT317", "display": "Likely inborn error of metabolism - WGS", "extension": [ @@ -100,7 +100,7 @@ { "coding": [ { - "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService", + "system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices", "code": "TP229", "display": "Likely inborn error of metabolism", "extension": [ diff --git a/StructureDefinition/NHSEngland-ServiceRequest-Genomics.json b/StructureDefinition/NHSEngland-ServiceRequest-Genomics.json index bcdd207b..fa2ec57d 100644 --- a/StructureDefinition/NHSEngland-ServiceRequest-Genomics.json +++ b/StructureDefinition/NHSEngland-ServiceRequest-Genomics.json @@ -2,11 +2,11 @@ "resourceType": "StructureDefinition", "id": "NHSEngland-ServiceRequest-Genomics", "url": "https://fhir.nhs.uk/StructureDefinition/NHSEngland-ServiceRequest-Genomics", - "version": "0.3.0", + "version": "0.3.1", "name": "NHSEngland_ServiceRequest_Genomics", "title": "NHSEngland ServiceRequest Genomics", "status": "active", - "date": "2026-04-16", + "date": "2026-08-11", "publisher": "NHS England", "contact": [ { @@ -288,7 +288,7 @@ { "id": "ServiceRequest.code.coding:DGTSCode.system", "path": "ServiceRequest.code.coding.system", - "fixedUri": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService" + "fixedUri": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices" }, { "id": "ServiceRequest.orderDetail", @@ -483,7 +483,7 @@ { "id": "ServiceRequest.reasonCode:DGTSTestPackage.coding.system", "path": "ServiceRequest.reasonCode.coding.system", - "fixedUri": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService" + "fixedUri": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices" }, { "id": "ServiceRequest.reasonReference",