BANCCO+ A CNV database to reduce diagnostic wandering, identify new genes, and expand our knowledge of the human genome Genetics/HeredityRare diseasesFamilies
FACE.S-4-KIDS A deep-phenotyping database using artificial intelligence to study craniofacial anomalies during development Rare diseasesGenetics/HeredityFamilies
FG-CoALS Franco-German cohort study on factors associated with weight loss in amyotrophic lateral sclerosis (ALS) Rare diseasesAdults
PAMPERO Towards personalized medicine in a rare genetic vascular disease: Rendu-Osler disease Genetics/HeredityRare diseasesFamilies
PROGRESS FSHD Remote assessment and artificial intelligence to validate new measures, biomarkers, and therapeutic targets for facioscapulohumeral muscular dystrophy (FSHD) Rare diseasesDatabases
RaDiCo - ECYSCO European cystinosis cohort: new biomarkers and new therapeutic approaches Genetics/HeredityRare diseasesFamilies
RASores Preclinical approaches for the treatment of RASopathy patients through a multi-omic study of their pathophysiology using a deeply phenotyped cohort in a dedicated European registry Rare diseasesDatabasesGenetics/Heredity