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8 changes: 4 additions & 4 deletions Bundle/Bundle-NonWGSScenario3-FetusAsProband-Example.json
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Expand Up @@ -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": [
Expand Down Expand Up @@ -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": [
Expand Down Expand Up @@ -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": [
Expand All @@ -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": [
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Original file line number Diff line number Diff line change
Expand Up @@ -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": [
Expand Down Expand Up @@ -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": [
Expand Down Expand Up @@ -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": [
Expand Down Expand Up @@ -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": [
Expand Down Expand Up @@ -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": [
Expand All @@ -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": [
Expand Down Expand Up @@ -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": [
Expand All @@ -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": [
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Original file line number Diff line number Diff line change
Expand Up @@ -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": [
Expand Down Expand Up @@ -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": [
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Original file line number Diff line number Diff line change
Expand Up @@ -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": [
Expand All @@ -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": [
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6 changes: 3 additions & 3 deletions Bundle/Bundle-NonWGSTestOrderForm-Example.json
Original file line number Diff line number Diff line change
Expand Up @@ -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": [
Expand All @@ -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": [
Expand Down Expand Up @@ -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"
}
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6 changes: 3 additions & 3 deletions Bundle/Bundle-NonWGSTestOrderForm-FetalScenario-Example.json
Original file line number Diff line number Diff line change
Expand Up @@ -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": [
Expand Down Expand Up @@ -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": [
Expand Down Expand Up @@ -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": [
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6 changes: 3 additions & 3 deletions Bundle/Bundle-NonWGSTestOrderForm-Reanalysis-Example.json
Original file line number Diff line number Diff line change
Expand Up @@ -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": [
Expand All @@ -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": [
Expand Down Expand Up @@ -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"
}
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Original file line number Diff line number Diff line change
Expand Up @@ -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": [
Expand All @@ -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": [
Expand Down Expand Up @@ -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"
}
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Expand Up @@ -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": [
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4 changes: 2 additions & 2 deletions Bundle/Bundle-TransactionResponseSuccess-Example.json
Original file line number Diff line number Diff line change
Expand Up @@ -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": [
Expand All @@ -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": [
Expand Down
6 changes: 3 additions & 3 deletions Bundle/Bundle-WGSTestOrderForm-Example.json
Original file line number Diff line number Diff line change
Expand Up @@ -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": [
Expand All @@ -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": [
Expand Down Expand Up @@ -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"
}
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2 changes: 1 addition & 1 deletion Bundle/CommunityCloud-Bundle-Example.json
Original file line number Diff line number Diff line change
Expand Up @@ -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"
}
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2 changes: 1 addition & 1 deletion Condition/Condition-MonogenicHearingLoss-Example.json
Original file line number Diff line number Diff line change
Expand Up @@ -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"
}
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2 changes: 1 addition & 1 deletion Observation/Observation-DiseasePenetrance-Example.json
Original file line number Diff line number Diff line change
Expand Up @@ -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"
}
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Original file line number Diff line number Diff line change
Expand Up @@ -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"
}
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Original file line number Diff line number Diff line change
Expand Up @@ -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"
}
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Original file line number Diff line number Diff line change
Expand Up @@ -85,13 +85,5 @@
},
"display": "anywhere place"
}
],
"link": [
{
"other": {
"reference": "https://api.service.nhs.uk/personal-demographics/FHIR/R4/Patient/9449307946"
},
"type": "seealso"
}
]
}
2 changes: 1 addition & 1 deletion Procedure/CommunityCloud-GenomicStudy-Example.json
Original file line number Diff line number Diff line change
Expand Up @@ -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"
}
Expand Down
Original file line number Diff line number Diff line change
Expand Up @@ -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": [
Expand Down Expand Up @@ -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": [
Expand Down
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