Research programs, registries, and trials
Orphanet and GARD — the rare-disease reference rails
establishedresearch program
Orphanet (ORPHA:75531) and NIH GARD carry the reference-level disease records that anchor subtype nomenclature and prevalence estimates for rare-disease infrastructure. Indexed as reference rails rather than primary evidence.
| Subtype scope | all EDS types |
|---|---|
| Criteria era | era-independent |
| Reviewed | 2026-09-16 |
Evidence
registryregistry report