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The IgG4-RD Registry is an anonymised database of patients with IgG4-RD.

This European database was set up with the aim of establishing the epidemiology, clinical course, resonse to treatment and prognoisis attributed to IgG4-RD.

The registry is supported by an EASL Registry studies Grant.

If you wish to participate in the study or to find out more infomation, please click here

For clinicians who wish to recruit patients to the registry, please click here