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[IOPS-4537] Correcting DGTS URL
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51 files changed

Lines changed: 99 additions & 99 deletions

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‎Bundle/Bundle-NonWGSScenario3-FetusAsProband-Example.json‎

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"code": {
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"coding": [
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{
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService",
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "GT1133",
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"display": "Common aneuploidy testing",
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"extension": [
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{
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"coding": [
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{
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService",
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "TP289",
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"display": "Common aneuploidy testing - prenatal",
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"extension": [
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"code": {
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"coding": [
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{
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService",
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "GT1133",
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"display": "Common aneuploidy testing",
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"extension": [
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{
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"coding": [
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{
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService",
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "TP289",
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"display": "Common aneuploidy testing - prenatal",
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"extension": [

‎Bundle/Bundle-NonWGSScenario4-ProbandWithMultipleFetus-Example.json‎

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"code": {
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"coding": [
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{
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService",
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "GT1133",
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"display": "Common aneuploidy testing",
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"extension": [
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{
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"coding": [
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{
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService",
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "TP289",
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"display": "Common aneuploidy testing - prenatal",
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"extension": [
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"code": {
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"coding": [
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{
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService",
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "GT1133",
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"display": "Common aneuploidy testing",
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"extension": [
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{
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"coding": [
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{
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService",
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "TP289",
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"display": "Common aneuploidy testing - prenatal",
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"extension": [
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"code": {
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"coding": [
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{
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService",
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "GT1133",
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"display": "Common aneuploidy testing",
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"extension": [
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{
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"coding": [
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{
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService",
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "TP289",
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"display": "Common aneuploidy testing - prenatal",
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"extension": [
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"code": {
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"coding": [
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{
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService",
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "GT1133",
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"display": "Common aneuploidy testing",
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"extension": [
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{
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"coding": [
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{
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService",
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "TP289",
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"display": "Common aneuploidy testing - prenatal",
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"extension": [

‎Bundle/Bundle-NonWGSScenario5-ProductsofConception-Example.json‎

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"code": {
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"coding": [
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{
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService",
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "GT1133",
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"display": "Common aneuploidy testing",
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"extension": [
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{
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"coding": [
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService",
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "TP289",
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"display": "Common aneuploidy testing - prenatal",
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"extension": [

‎Bundle/Bundle-NonWGSTestOrderForm-CancerSolidTumor-Example.json‎

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"code": {
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"coding": [
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService",
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "GT1046",
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"display": "Paediatric Tumour Differential Diagnosis - NGS Panel SNV and CNV",
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"extension": [
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{
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"coding": [
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService",
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "TP550",
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"display": "Paediatric Tumours",
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"extension": [

‎Bundle/Bundle-NonWGSTestOrderForm-Example.json‎

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"code": {
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"coding": [
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService",
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "GT488",
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"display": "Monogenic hearing loss - Panel sequencing",
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"extension": [
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{
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"coding": [
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService",
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "TP439",
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"display": "Monogenic hearing loss",
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"extension": [
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"code": {
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"coding": [
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{
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService",
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "TP439",
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"display": "Monogenic hearing loss"
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}

‎Bundle/Bundle-NonWGSTestOrderForm-FetalScenario-Example.json‎

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{
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"coding": [
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{
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService",
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "TP289",
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"display": "Common aneuploidy testing - prenatal",
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"extension": [
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"coding": [
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService",
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "TP289",
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"display": "Common aneuploidy testing - prenatal",
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"extension": [
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{
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"coding": [
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService",
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "TP289",
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"display": "Common aneuploidy testing - prenatal",
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"extension": [

‎Bundle/Bundle-NonWGSTestOrderForm-Reanalysis-Example.json‎

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"code": {
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"coding": [
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService",
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "GT192",
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"display": "Reanalysis of existing data",
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"extension": [
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{
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"coding": [
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{
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService",
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "TP459",
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"display": "Paediatric disorders",
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"extension": [
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"code": {
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"coding": [
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService",
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "TP439",
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"display": "Monogenic hearing loss"
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}

‎Bundle/Bundle-NonWGSTestOrderFormQRPatientExtensions-Example.json‎

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"code": {
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"coding": [
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestService",
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "GT488",
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"display": "Monogenic hearing loss - Panel sequencing",
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"extension": [
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"coding": [
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "TP439",
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"display": "Monogenic hearing loss",
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"code": {
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"coding": [
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "TP439",
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"display": "Monogenic hearing loss"
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}

‎Bundle/Bundle-NonWGSTestOrderFormUpdated-FetalScenario-Example.json‎

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{
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"coding": [
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "TP289",
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"display": "Common aneuploidy testing - prenatal",
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"extension": [

‎Bundle/Bundle-TransactionResponseSuccess-Example.json‎

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"code": {
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"coding": [
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "GT488",
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"display": "Monogenic hearing loss - Panel sequencing",
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"coding": [
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"system": "https://fhir.nhs.uk/CodeSystem/England-DigitalGenomicTestServices",
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"code": "TP439",
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"display": "Monogenic hearing loss",
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"extension": [

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