There are between 7,000 and 8,000 rare diseases (fewer than 5 people affected out of 10,000), over 80% of which are genetic in origin. These diseases affect around 3 million people in France. However, despite recent successes in diagnosis, care and the development of treatments, 50% of patients still have no molecular diagnosis and less than 5% of patients benefit from treatment. 

The aim of the Marseille institute for rare diseases (MarMaRa) is to bring together research, medical and educational teams, as well as partners from industry, in cross-disciplinary training and research initiatives.

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The institute as seen by its members


 

Our sites

The MarMaRa institute brings together teams on 7 university and scientific sites.

Find out more about the Institute

Meet our teams

Governance

Executive office, teams, institute council, committees, STAB...

Our partner structures

Ecosystem

Laboratories, faculties, doctoral schools,…