MyThalassaemia is a national registry for thalassaemia disease. Thalassaemia is a hereditary blood disorder and is common in countries stretching from the Mediterranean to South East Asia. Our web-based system captures extensive laboratory and treatment data and produces valuable reports for monitoring and formulation of national policy for curbing the spread of thalassaemia. The registry holds the diagnosis and treatment records of all thalassaemia patients in the country. Extensive reporting and analysis based on centres, states or national data makes it a useful reporting tool for monitoring and planning purposes for different levels of health professionals.
We are proud to have designed, developed and maintain the national thalassaemia registry for the Ministry of Health Malaysia.