Established as an informal group in 1983 and becoming a society in 1994, the European Society for Immunodeficiencies (ESID) is a non-profit organization with data across several countries of Europe whose main objectives are to facilitate the exchange of ideas and information among doctors, nurses, biomedical investigators, patients and their families concerned with primary immunodeficiency diseases and also to promote research on causes, mechanisms and treatment of these disorders.
The aim of the ESID registry is to build a common data pool and estimate the disease burden of primary immunodeficiencies (PID) in Europe and to provide an internet-based database for clinical and research data on patients with PID.
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