se-atlas: Kartierung von Versorgungseinrichtungen und Patientenorganisationen für Menschen mit Seltenen Erkrankungen

se-atlas is the new care atlas for people with rare diseases.

Help se-atlas growing.

We are looking forward to your feedback.

Core facilities for rare diseases (ZSE) in se-atlas serve as point of contact for the care of patients with rare diseases.

You don't know your diagnosis yet?

Contact a centre for rare diseases or another parent facility close to you.
The on-site guides are pleased to be available as a contact for your treating physician.
Overview of the core facilities for rare diseases (ZSE)
Would you like to add a facility for rare diseases or a support group organisation?

If you are a representative of a facility for rare diseases or a support group organisation that is not listed yet you are welcome to register yourself and then enter this information.
Register now
Would you like to learn more about se-atlas?

You can find more information about se-atlas at the following links.
If you have further questions, feel free to contact the project team directly.
The se-atlas research project
Frequently asked questions about se-atlas - FAQ
Contact information