NHS North West Genomics - Local Development build (v2.2.0) built by the FHIR (HL7® FHIR® Standard) Build Tools. See the Directory of published versions

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ConceptMap: Genomic Clinical Indication (M*) to Digital Genomic Test Services (TP)

Official URL: https://fhir.nwgenomics.nhs.uk/ConceptMap/GenomicClinicalIndicationToDigitalGenomicTestServices				Version: 2.2.0	Highlight text changes?
Active as of 2026-09-20					Computable Name: GenomicClinicalIndicationToDigitalGenomicTestServices

Legacy 1st-level clinical-indication numbers (GenomicClinicalIndication) for Haematological Oncology and Cancer CNS, mapped to the TP* codes that replace them - derived from the same Legacy 'M' codes column used for the GT* map above (each legacy code's leading number, cross-referenced against which TP its row belongs to), since NHS England's spreadsheets don't name the old CI number directly. Genuinely many-to-many for a large share of these: the old haem-onc CI grouping was organised around a shared assay/test method, not disease, so one old CI number routinely feeds several disease-specific TPs - recorded as multiple targets with equivalence = #relatedto, not forced to one.

Display text for the old CI numbers has no live source any more (see notebook 14's own note on this) - taken from the current EnglandTestCode.fsh's own M*.* entries for that number.

Built by nw-gmsa/Testing notebook 14, checked against v1.1/v2 on 2026-09-08.