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

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 March 20...

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Detalles Bibliográficos
Autores principales: Pichon, Thibaut, Messiaen, Claude, Soussand, Louis, Angin, Céline, Sandrin, Arnaud, Elarouci, Nabila, Jannot, Anne-Sophie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Letter to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10318625/
https://www.ncbi.nlm.nih.gov/pubmed/37400917
http://dx.doi.org/10.1186/s13023-023-02725-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10318625/
https://www.ncbi.nlm.nih.gov/pubmed/37400917
http://dx.doi.org/10.1186/s13023-023-02725-2

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