ERKNet Patients Registry: Registry Reports

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ERKReg

The European Rare Kidney Disease Registry

1^st of March 2021

We are pleased to present the first ERKReg report in layman`s language. This report summarized in an easy language the Registry design, objectives and features.

Layman ERKReg Registry Report (PDF)

We present the first Annual ERKReg Registry Report, which provides information on disease demographics and the quality of treatment performance in children and adults with rare kidney conditions.

Annual Registry Report 2019 (PDF)

This website is part of the project / joint action "777304 / ERK-REG" which has received funding from the European Union’s Health Programme (2014-2020)