Overview of patients’ cohorts in the French National rare disease registry

Overview of patients’ cohorts in the French National rare disease registry

Abstract In France, all patients followed by Rare Disease (RD) expert centers have to be registered in the National Rare Disease Registry (BNDMR). This database collects a minimum data set including diagnosis coded using the Orphanet nomenclature. Overall, 753,660 patients were recorded from 2007 to...

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Bibliographic Details
Main Authors: Thibaut Pichon, Claude Messiaen, Louis Soussand, Céline Angin, Arnaud Sandrin, Nabila Elarouci, Anne-Sophie Jannot, on behalf of the BNDMR infrastructure team
Format: Article
Language:English
Published: BMC 2023-07-01
Series:Orphanet Journal of Rare Diseases
Online Access:https://doi.org/10.1186/s13023-023-02725-2

Internet

https://doi.org/10.1186/s13023-023-02725-2

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