International Niemann–Pick Disease Alliance

Information Portal

The INPDA Information Portal is a shared space that offers access to information and resources relating to Niemann-Pick disease. The Portal brings together a wide range of helpful information for patients, their families and the professionals working in this field, in different languages and formats. The ultimate aim is to maximise use of resources, minimise duplication and encourage collaboration. All of the information and resources included here are downloadable and may be shared across your networks. There is also the option to adapt a particular article/resource for use within your patient community; if you wish to do this, please contact info@inpda.org.

Please note that the information provided via this website is intended for general educational and informative purposes only. It is not intended as a substitute to medical or professional services nor should it replace the relationship that exists between patients, their physicians and other health care providers. Please see below for a link to our full Disclaimer Statement.

Join the Registry

Calling all patients and carers! We've created a global registry of all NPD patients - if you're not enrolled yet, join us now...

Think Again. Think NP-C

Join our international campaign to improve diagnosis of NP-C!