Skip to main content
Log in
European Commission
Dutch nl

Dialog

Select your language

български español čeština dansk Deutsch eesti ελληνικά English français Gaeilge hrvatski italiano
latviešu lietuvių magyar Malti Nederlands polski português română slovenčina slovenščina suomi svenska
You are here:
  1. European CommissionEU Science Hub
  2. European Platform on Rare Disease Registration
  3. Node
  4. 63

Prevention and risk factors

  • EUROCAT Network overview

    Primary Prevention

    A European network of population-based registries for the epidemiologic surveillance of congenital anomalies.

     
  • Objectives of EUROCAT

    Folic Acid and Neural Tube Defects

    Provide epidemiologic information on congenital anomalies, evaluates and acts as an information and resource center both for the population and health professionals.

     
  • JRC-EUROCAT Central Registry

    Congenital Rubella Syndrome

    The Central Registry supports the coordinating activities, manages the data and acts as a Contact Point.

     
  • EUROCAT Association

    Medication During Pregnancy

    Consists of the members of the Steering Committee and the Member Registries. Find here more information, contacts and details: Member Registries in a close-up.

     
  • Coding Committee

    Environmental Pollution

    Aims to improve standardised coding and classification of congenital anomalies by giving advice and guidance to registries.

     
  •  

European Platform on Rare Disease Registration

  • Contact
  • Cookies
  • Privacy statement

European Commission

  • European Commission website

Follow the European Commission

  • Facebook
  • Twitter
  • Other social media

European Union

  • EU institutions
  • European Union
  • About the Commission's new web presence
  • Resources for partners
  • Legal notice
  • Contact