RaReTiA
Creation of a rare eye disease data warehouse (FREDD) and an AI pilot project for pigmentary retinopathies
Retinitis pigmentosa (RP), an inherited retinal dystrophy, is a major cause of visual impairment.
Project objective
The RaReTiA project aims primarily to establish a national health data warehouse within the France Cohortes information system and to address its first scientific challenges.
Governance
Scientific and Technical Lead:
Prof. Hélène DOLLFUS, Inserm UMRS_1112 – Laboratory of Medical Genetics & University of Strasbourg
Further information
FREDD-EDS website (click on the link)
No news has been published for this cohort, you can consult all the news in the spotlight section