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Ehlers-Danlos syndrome

The Ehlers–Danlos syndromes (EDS) are a clinically and genetically heterogeneous group of heritable connective tissue disorders (HCTDs) characterized by joint hypermobility, skin hyperextensibility, and tissue fragility.

20 trials tagged with this condition →

Ehlers-Danlos syndrome, hypermobility type 15 trials
Joint laxity, familial 14 trials
Ehlers-Danlos syndrome, vascular type 6 trials Sub-types →
Bethlem myopathy 2 0 trials
COL1A1-related Ehlers-Danlos syndrome 0 trials Sub-types →
COL1A2-related Ehlers-Danlos syndrome 0 trials Sub-types →
Ehlers-Danlos syndrome due to tenascin-X deficiency 0 trials
Ehlers-Danlos syndrome, Beasley-Cohen type 0 trials
Ehlers-Danlos syndrome, arthrochalasia type 0 trials Sub-types →
Ehlers-Danlos syndrome, autosomal dominant, type unspecified 0 trials
Ehlers-Danlos syndrome, classic type 0 trials Sub-types →
Ehlers-Danlos syndrome, classic-like, 2 0 trials
Ehlers-Danlos syndrome, classic-like, 3 0 trials
Ehlers-Danlos syndrome, dermatosparaxis type 0 trials
Ehlers-Danlos syndrome, fibronectinemic type 0 trials
Ehlers-Danlos syndrome, kyphoscoliotic type 1 0 trials
Ehlers-Danlos syndrome, kyphoscoliotic type, 2 0 trials
Ehlers-Danlos syndrome, musculocontractural type 0 trials Sub-types →
Ehlers-Danlos syndrome, periodontitis type 0 trials Sub-types →
Ehlers-Danlos syndrome, spondylodysplastic type 0 trials Sub-types →
Ehlers-Danlos syndrome, vascular-like type 0 trials
Ehlers-Danlos/osteogenesis imperfecta syndrome 0 trials Sub-types →
X-linked Ehlers-Danlos syndrome 0 trials
Brittle cornea syndrome 0 trials Sub-types →
Spondylodysplastic Ehlers-Danlos syndrome 0 trials