Clinical Genetics Society



The Clinical Genetics Society (CGS) was founded in 1970 to bring together doctors and other professionals involved in the care of individuals and families with genetic disorders.

Rare Diseases: Make sure your voice is heard

In July, the Minister for rare disease at the Department for Health and Social Care, Baroness Blackwood, announced a ‘national conversation’ on rare disease. This conversation aims to gather a range of views from the rare disease community.  The views collected from patients, healthcare professionals including GPs, specialist rare disease clinicians, clinical academics, and industry will be used by government to inform a rare disease framework to improve the lives of people living with rare diseases. This will follow on from the current UK Rare Diseases Strategy, which expires at the end of 2020.
To start the conversation, a survey has been launched to understand the major barriers that healthcare professionals working with rare diseases face.
Make sure your voice is heard by completing the short survey using the link below by Friday 29thNovember 2019.
Please share the survey link with your relevant networks and colleagues to ensure a wide range of views are captured. 
Dr Frances Elmslie
President, Clinical Genetics Society

Trainees in Clinical Genetics

The CGS is committed to facilitating high standards of training for Specialist Registrars (SpRs or Trainees) in Clinical Genetics. The CGS is represented on the Specialist Advisory Committee (SAC).