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The organisation was founded by the parents of a child diagnosed with IC-MPGN.[1]
CompCure works to increase knowledge and awareness of C3G and IC-MPGN, including improving diagnosis, supporting research, contributing to the development of patient registries, promoting the use of clinical guidelines, and supporting the development of new therapies.[1]
The organisation collaborates with patients, healthcare professionals, industry partners, and other stakeholders.[1]
CompCure contributes to a subregistry within the European Rare Kidney Disease Reference Network (ERKNet), one of 24 European Reference Networks supported by the European Union.[2][3]
ERKNet comprises more than 100 specialised centres across 24 countries.[4]
The network has established the European Rare Kidney Registry (ERKReg), which includes data from more than 70,000 patients with rare kidney diseases.[5]
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