Information portal on Hereditary Angioedema (HAE)

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This document was printed on 06.Jan.2009.

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National organisations

HAE lobbyists and organisations in Europe: initiatives, medical associations and patient organisations

By clicking on the European map or by using the listbox you will find contact information and short descriptions of national patient or medical organisations, initiatives and associations dealing with HAE or rare diseases in general. If available, the list will show a link to specific webpages. The list is updated regularly. Please send us your comments and suggestions by E-mail.




Austria [AT]Belgium [BE]Croatia [HR]Denmark [DK]France [FR]Germany [DE]Hungary [HU]Italy [IT]Netherlands [NL]Norway [NO]Poland [PL]Spain [ES]Sweden [SE]Switzerland [CH]Ukraine [UA]United Kingdom [UK]
Resuming information
Frequently inquired
Author: Jerini AG
Source: HAE Network
Status:10/07

This list is frequently updated. Please send us your comments, suggestions or change requests by Email.

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