EuRReca (European Registries for Rare Endocrine Conditions) is funded by EU Health Programme and supported by the European Society for Paediatric Endocrinology (ESPE) and the European Society of Endocrinology (ESE).

EuRRECa’s aim is to maximize the opportunity for all patients, healthcare professionals and researchers to participate and use high‐quality, patient‐centred registries for rare endocrine conditions that are covered within Endo‐ERN (the European Reference Network on Rare Endocrine Conditions)

The project was launched in February 2018.