Welcome To The NHR

The National Haemoglobinopathy Registry (NHR) is a database of patients with red cell disorders (mainly Sickle Cell Disease and Thalassaemia Major) living in the UK. This new database collects data,which is required by the Department of Health from Haemoglobinopathy centres. The central aim of the registry is to improve patient care.

National Haemoglobinopathy Registry Annual Report 

 Click the image above to view the National Haemoglobinopathy Registry Annual Report for 2013/14

Log In To The Secure NHR System.

Click the image above to log in (You can only log in if you are on the NHS network only)


Please see below for a list of summarised reports from the NHR. These reports are updated periodically, the last update was on the 29th December 2016

Contact Us

If you require any assistance, guidance or information that is not available on the website, please contact our support team on 0161 277 7917 or email: support@mdsas.com