Removing GMS V2 Requesting Reason

Removing GMS V2 Requesting Reason

Author: KazeemHamzat

Library/Library-DGTS-GT46-Example.json

@@ -16,7 +16,7 @@
   {
    "name": "additional_panels_available",
    "use": "in",
-   "max": "1",
+   "max": "*",
    "type": "Coding"
   },
   {

PlanDefinition/PlanDefinition-DGTS_TP231-Example.json

@@ -84,66 +84,6 @@
   }
  ],
  "useContext": [
-  {
-   "code": {
-    "code": "user",
-    "system": "http://terminology.hl7.org/CodeSystem/usage-context-type"
-   },
-   "valueCodeableConcept": {
-    "coding": [
-     {
-      "code": "400",
-      "system": "https://fhir.hl7.org.uk/CodeSystem/UKCore-PracticeSettingCode",
-      "display": "Neurology"
-     }
-    ]
-   }
-  },
-  {
-   "code": {
-    "code": "user",
-    "system": "http://terminology.hl7.org/CodeSystem/usage-context-type"
-   },
-   "valueCodeableConcept": {
-    "coding": [
-     {
-      "code": "420",
-      "system": "https://fhir.hl7.org.uk/CodeSystem/UKCore-PracticeSettingCode",
-      "display": "Paediatrics"
-     }
-    ]
-   }
-  },
-  {
-   "code": {
-    "code": "user",
-    "system": "http://terminology.hl7.org/CodeSystem/usage-context-type"
-   },
-   "valueCodeableConcept": {
-    "coding": [
-     {
-      "code": "311",
-      "system": "https://fhir.hl7.org.uk/CodeSystem/UKCore-PracticeSettingCode",
-      "display": "Clinical Genetics"
-     }
-    ]
-   }
-  },
-  {
-   "code": {
-    "code": "focus",
-    "system": "http://terminology.hl7.org/CodeSystem/usage-context-type"
-   },
-   "valueCodeableConcept": {
-    "coding": [
-     {
-      "system": "https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics",
-      "code": "diagnostic",
-      "display": "Diagnostic"
-     }
-    ]
-   }
-  },
   {
    "code": {
     "code": "focus",

PlanDefinition/PlanDefinition-DGTS_TP383-Example.json

@@ -83,66 +83,6 @@
   }
  ],
  "useContext": [
-  {
-   "code": {
-    "code": "user",
-    "system": "http://terminology.hl7.org/CodeSystem/usage-context-type"
-   },
-   "valueCodeableConcept": {
-    "coding": [
-     {
-      "code": "420",
-      "system": "https://fhir.hl7.org.uk/CodeSystem/UKCore-PracticeSettingCode",
-      "display": "Paediatrics"
-     }
-    ]
-   }
-  },
-  {
-   "code": {
-    "code": "user",
-    "system": "http://terminology.hl7.org/CodeSystem/usage-context-type"
-   },
-   "valueCodeableConcept": {
-    "coding": [
-     {
-      "code": "400",
-      "system": "https://fhir.hl7.org.uk/CodeSystem/UKCore-PracticeSettingCode",
-      "display": "Neurology"
-     }
-    ]
-   }
-  },
-  {
-   "code": {
-    "code": "user",
-    "system": "http://terminology.hl7.org/CodeSystem/usage-context-type"
-   },
-   "valueCodeableConcept": {
-    "coding": [
-     {
-      "code": "311",
-      "system": "https://fhir.hl7.org.uk/CodeSystem/UKCore-PracticeSettingCode",
-      "display": "Clinical Genetics"
-     }
-    ]
-   }
-  },
-  {
-   "code": {
-    "code": "focus",
-    "system": "http://terminology.hl7.org/CodeSystem/usage-context-type"
-   },
-   "valueCodeableConcept": {
-    "coding": [
-     {
-      "system": "https://fhir.nhs.uk/CodeSystem/rare-diseaseTesting-genomics",
-      "code": "diagnostic",
-      "display": "Diagnostic"
-     }
-    ]
-   }
-  },
   {
    "code": {
     "code": "focus",