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Ehlers-Danlos syndrome

MONDO:0020066

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.

Also known as: Danlos Disease, Ehlers, Danlos disease, Disease, Ehlers Danlos, Disease, Ehlers-Danlos, Dystrophia mesodermalis congenita, EDS, Ehler Danlos Syndrome, Ehlers Danlos Disease

46 clinical trials for this condition and its sub-types.

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Sub-types

Ehlers-Danlos syndrome, hypermobility type (15) Joint laxity, familial (14) Ehlers-Danlos syndrome, vascular type (6) Autosomal dominant Ehlers-Danlos syndrome, vascular type (0) Autosomal recessive Ehlers-Danlos syndrome, vascular type (0) Bethlem myopathy 2 (0) Brittle cornea syndrome (0) Brittle cornea syndrome 1 (0) Brittle cornea syndrome 2 (0) COL1A1-related Ehlers-Danlos syndrome (0) COL1A2-related Ehlers-Danlos syndrome (0) Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 1 (0) Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 2 (0) Ehlers-Danlos/osteogenesis imperfecta syndrome (0) Ehlers-Danlos syndrome, arthrochalasia type (0) Ehlers-Danlos syndrome, arthrochalasia type, 2 (0) Ehlers-Danlos syndrome, autosomal dominant, type unspecified (0) Ehlers-Danlos syndrome, Beasley-Cohen type (0) Ehlers-Danlos syndrome, cardiac valvular type (0) Ehlers-Danlos syndrome, classic-like, 2 (0)

Broader categories

Disease (680) Hereditary disease (176) Syndromic disease (25) Human disease (14) Developmental defect during embryogenesis (8) Disease of genetic or genomic mechanism (2) Disease by body system or component (0) Disease by developmental or physiological process (0) Disease by etiologic mechanism (0) Disorder of development or morphogenesis (0)

Trials to join now! 17 Not yet recruiting 8 Not yet finished but already full! 7 Completed 12 Terminated 2