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 scopeall EDS types
Criteria eraera-independent
Reviewed2026-09-16

Evidence

registryregistry report