North West Genomic Medicine Service Alliance
0.0.1 - ci-build
DRAFT Implementation Guide
This is for collaboration and discussion purposes and is subject to change.
North West Genomic Medicine Service Alliance - Local Development build (v0.0.1) built by the FHIR (HL7® FHIR® Standard) Build Tools. See the Directory of published versions
Official URL: https://nw-gmsa.github.io/ValueSet/order-category | Version: 0.0.1 | |||
Draft as of 2025-06-19 | Computable Name: OrderCategory |
Top level classification of Genomic Test Directory
References
This value set includes codes based on the following rules:
https://nw-gmsa.github.io/CodeSystem/nwgmsa
Code | Display |
RareAndInheritedDiseasesGeneticTesting | Rare and inherited diseases Genetic Testing (procedure) |
PreNatalGeneticTesting | Pre Natal Genetic Testing (procedure) |
HaemoglobinopathyGeneticTesting | Haemoglobinopathy Genetic Testing (procedure) |
CancerGeneticTesting | Cancer Genetic Testing (procedure) |
http://snomed.info/sct
Code | Display |
1186936003 | Storage of specimen (procedure) |
No Expansion for this valueset (Unknown Code System)
Explanation of the columns that may appear on this page:
Level | A few code lists that FHIR defines are hierarchical - each code is assigned a level. In this scheme, some codes are under other codes, and imply that the code they are under also applies |
System | The source of the definition of the code (when the value set draws in codes defined elsewhere) |
Code | The code (used as the code in the resource instance) |
Display | The display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application |
Definition | An explanation of the meaning of the concept |
Comments | Additional notes about how to use the code |