Send to

Choose Destination
See comment in PubMed Commons below
Ned Tijdschr Geneeskd. 2008 Mar 1;152(9):518-9.

[Orphanet: a European database for rare diseases].

[Article in Dutch]

Author information

VU Medisch Centrum, afd. Klinische Genetica, sectie Community Genetics/EMGO Instituut, BS7 D424, Postbus 7057, 1007 MB Amsterdam.


Orphanet is a European initiative that aims to improve the management and treatment of rare diseases. It comprises a database dedicated to information on rare diseases and orphan drugs, and offers services adapted to the needs of patients and their families, health professionals, and researchers. The database can be accessed through the website ( and has some interesting options for searching, for example research projects, support groups or searching by clinical signs. Health professionals are encouraged to add activities concerning rare diseases to the database.

[Indexed for MEDLINE]
PubMed Commons home

PubMed Commons

How to join PubMed Commons

    Supplemental Content

    Loading ...
    Support Center