Added Clinical Specialty

KazeemHamzat · KazeemHamzat · commit 4a0f7abda4ab · 2026-06-29T12:21:01.000+01:00
Added Clinical Specialty to PlanDefinition
diff --git a/.simplifier/folder.settings.json b/.simplifier/folder.settings.json
diff --git a/Bundle/Bundle-DGTS-GenomicTest-Catalogue-Example.json b/Bundle/Bundle-DGTS-GenomicTest-Catalogue-Example.json
@@ -148,6 +148,21 @@
         }
        ]
       }
+     },
+     {
+      "code": {
+       "code": "focus",
+       "system": "http://terminology.hl7.org/CodeSystem/usage-context-type"
+      },
+      "valueCodeableConcept": {
+       "coding": [
+        {
+         "system": "https://fhir.nhs.uk/CodeSystem/DGTS-clinical-specialty-genomics",
+         "code": "fetal-and-prenatal",
+         "display": "Fetal and Prenata"
+        }
+       ]
+      }
      }
     ],
     "goal": [
@@ -341,6 +356,21 @@
         }
        ]
       }
+     },
+     {
+      "code": {
+       "code": "focus",
+       "system": "http://terminology.hl7.org/CodeSystem/usage-context-type"
+      },
+      "valueCodeableConcept": {
+       "coding": [
+        {
+         "system": "https://fhir.nhs.uk/CodeSystem/DGTS-clinical-specialty-genomics",
+         "code": "fetal-and-prenatal",
+         "display": "Fetal and Prenata"
+        }
+       ]
+      }
      }
     ],
     "goal": [
diff --git a/PlanDefinition/PlanDefinition-DGTS_TP231-Example.json b/PlanDefinition/PlanDefinition-DGTS_TP231-Example.json
@@ -143,14 +143,29 @@
      }
     ]
    }
+  },
+  {
+   "code": {
+    "code": "focus",
+    "system": "http://terminology.hl7.org/CodeSystem/usage-context-type"
+   },
+   "valueCodeableConcept": {
+    "coding": [
+     {
+      "system": "https://fhir.nhs.uk/CodeSystem/DGTS-clinical-specialty-genomics",
+      "code": "fetal-and-prenatal",
+      "display": "Fetal and Prenata"
+     }
+    ]
+   }
   }
  ],
  "goal": [
   {
    "description": {
     "coding": [
      {
-       "system": "https://fhir.nhs.uk/CodeSystem/DGTS-testpackage-modality",
+      "system": "https://fhir.nhs.uk/CodeSystem/DGTS-testpackage-modality",
       "code": "rare-and-inherited-disease",
       "display": "Rare and Inherited Disease"
      }
diff --git a/PlanDefinition/PlanDefinition-DGTS_TP383-Example.json b/PlanDefinition/PlanDefinition-DGTS_TP383-Example.json
@@ -142,6 +142,21 @@
      }
     ]
    }
+  },
+  {
+   "code": {
+    "code": "focus",
+    "system": "http://terminology.hl7.org/CodeSystem/usage-context-type"
+   },
+   "valueCodeableConcept": {
+    "coding": [
+     {
+      "system": "https://fhir.nhs.uk/CodeSystem/DGTS-clinical-specialty-genomics",
+      "code": "fetal-and-prenatal",
+      "display":"Fetal and Prenata"
+     }
+    ]
+   }
   }
  ],
  "goal": [

Original file line number	Diff line number	Diff line change
`@@ -148,6 +148,21 @@`
`148`	`148`	`}`
`149`	`149`	`]`
`150`	`150`	`}`
	`151`	`+ },`
	`152`	`+ {`
	`153`	`+ "code": {`
	`154`	`+ "code": "focus",`
	`155`	`+ "system": "http://terminology.hl7.org/CodeSystem/usage-context-type"`
	`156`	`+ },`
	`157`	`+ "valueCodeableConcept": {`
	`158`	`+ "coding": [`
	`159`	`+ {`
	`160`	`+ "system": "https://fhir.nhs.uk/CodeSystem/DGTS-clinical-specialty-genomics",`
	`161`	`+ "code": "fetal-and-prenatal",`
	`162`	`+ "display": "Fetal and Prenata"`
	`163`	`+ }`
	`164`	`+ ]`
	`165`	`+ }`
`151`	`166`	`}`
`152`	`167`	`],`
`153`	`168`	`"goal": [`
`@@ -341,6 +356,21 @@`
`341`	`356`	`}`
`342`	`357`	`]`
`343`	`358`	`}`
	`359`	`+ },`
	`360`	`+ {`
	`361`	`+ "code": {`
	`362`	`+ "code": "focus",`
	`363`	`+ "system": "http://terminology.hl7.org/CodeSystem/usage-context-type"`
	`364`	`+ },`
	`365`	`+ "valueCodeableConcept": {`
	`366`	`+ "coding": [`
	`367`	`+ {`
	`368`	`+ "system": "https://fhir.nhs.uk/CodeSystem/DGTS-clinical-specialty-genomics",`
	`369`	`+ "code": "fetal-and-prenatal",`
	`370`	`+ "display": "Fetal and Prenata"`
	`371`	`+ }`
	`372`	`+ ]`
	`373`	`+ }`
`344`	`374`	`}`
`345`	`375`	`],`
`346`	`376`	`"goal": [`
Original file line number	Diff line number	Diff line change
`@@ -143,14 +143,29 @@`
`143`	`143`	`}`
`144`	`144`	`]`
`145`	`145`	`}`
	`146`	`+ },`
	`147`	`+ {`
	`148`	`+ "code": {`
	`149`	`+ "code": "focus",`
	`150`	`+ "system": "http://terminology.hl7.org/CodeSystem/usage-context-type"`
	`151`	`+ },`
	`152`	`+ "valueCodeableConcept": {`
	`153`	`+ "coding": [`
	`154`	`+ {`
	`155`	`+ "system": "https://fhir.nhs.uk/CodeSystem/DGTS-clinical-specialty-genomics",`
	`156`	`+ "code": "fetal-and-prenatal",`
	`157`	`+ "display": "Fetal and Prenata"`
	`158`	`+ }`
	`159`	`+ ]`
	`160`	`+ }`
`146`	`161`	`}`
`147`	`162`	`],`
`148`	`163`	`"goal": [`
`149`	`164`	`{`
`150`	`165`	`"description": {`
`151`	`166`	`"coding": [`
`152`	`167`	`{`
`153`		`- "system": "https://fhir.nhs.uk/CodeSystem/DGTS-testpackage-modality",`
	`168`	`+ "system": "https://fhir.nhs.uk/CodeSystem/DGTS-testpackage-modality",`
`154`	`169`	`"code": "rare-and-inherited-disease",`
`155`	`170`	`"display": "Rare and Inherited Disease"`
`156`	`171`	`}`
Original file line number	Diff line number	Diff line change
`@@ -142,6 +142,21 @@`
`142`	`142`	`}`
`143`	`143`	`]`
`144`	`144`	`}`
	`145`	`+ },`
	`146`	`+ {`
	`147`	`+ "code": {`
	`148`	`+ "code": "focus",`
	`149`	`+ "system": "http://terminology.hl7.org/CodeSystem/usage-context-type"`
	`150`	`+ },`
	`151`	`+ "valueCodeableConcept": {`
	`152`	`+ "coding": [`
	`153`	`+ {`
	`154`	`+ "system": "https://fhir.nhs.uk/CodeSystem/DGTS-clinical-specialty-genomics",`
	`155`	`+ "code": "fetal-and-prenatal",`
	`156`	`+ "display":"Fetal and Prenata"`
	`157`	`+ }`
	`158`	`+ ]`
	`159`	`+ }`
`145`	`160`	`}`
`146`	`161`	`],`
`147`	`162`	`"goal": [`