EUROCAT is a network of population-based congenital anomaly registries providing standardized epidemiologic information on congenital anomalies in Europe. There are three types of EUROCAT membership: full, associate, or affiliate. Full member registries send individual records of all congenital anomalies covered by their region. Associate members transmit aggregate case counts for each EUROCAT anomaly subgroup by year and by type of birth. This article describes the organization and activities of each of the current 29 full member and 6 associate member registries of EUROCAT.
Greenlees, R., Neville, A., Addor, MC., Amar, E., Arriola, L., Bakker, M., Barisic, I., Boyd, PA., Calzolari, E., Doray, B., Draper, E., & et al, U. (2011). Paper 6: EUROCAT member registries: organization and activities. Birth Defects Research (Part A), 91(1), S51-S100. https://doi.org/10.1002/bdra.20775