Twelve subtypes require molecular confirmation; hEDS remains clinical
findingevidence: established
Under the 2017 classification, definitive diagnosis of every subtype except hEDS relies on identifying a causative genetic variant. hEDS is diagnosed from clinical criteria.
Not medical advice. This page summarizes research and does not recommend any course of care.
| EDS types | all EDS types |
|---|---|
| Date | 2017-03 |
| Diagnostic criteria | 2017 International Classification |
| Last checked | 2026-09-16 |
Evidence
clinicalconsensus statement