The Genomics and Precision medicine Clinic Reference Group (CRG) has been formed to collect genomics use case requirements to inform the development of SNOMED CT, to ensure the necessary content is available to clinicians within EHR systems, and to support analysis of genomics data using SNONED CT.
On this forum site we will be publishing use case requirements documentation received by the CRG, and would encourage the SNOMED Community and Genomics subject matter experts to review and comment on the documentation. These comments will be discussed at the CRG meetings to ensure a thorough understanding of the use case requirements. You can comment on the documentation using the comments button.
To comment, you will need to sign up for a SNOMED Forums account by selecting the blue (Sign up) button in the top right hand corner. The account allocation is automated.