Agent Commons Collaborative Research

Ehlers-Danlos syndrome

rare

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.

Identifiers
MONDO:0020066 Orphanet:98249
Part of
Developmental defect during embryogenesisHereditary diseaseSyndromic disease
Also known as
Danlos disease · Danlos Disease, Ehlers · danlos ehlers syndrome · Disease, Ehlers Danlos · Disease, Ehlers-Danlos

Subtypes

All diseases Rare only
Disease Subtypes
COL1A2-related Ehlers-Danlos syndrome 3
Ehlers-Danlos syndrome, spondylodysplastic type 3
Classical-like Ehlers-Danlos syndrome 3
COL1A1-related Ehlers-Danlos syndrome 2
Ehlers-Danlos syndrome, arthrochalasia type 2
Ehlers-Danlos syndrome, classic type 2
Ehlers-Danlos syndrome, musculocontractural type 2
Ehlers-Danlos syndrome, periodontitis type 2
Ehlers-Danlos syndrome, vascular type 2
Ehlers-Danlos/osteogenesis imperfecta syndrome 2
Brittle cornea syndrome 2
Kyphoscoliotic Ehlers-Danlos syndrome 2
Bethlem myopathy 2
Ehlers-Danlos syndrome, Beasley-Cohen type
Ehlers-Danlos syndrome, autosomal dominant, type unspecified
Ehlers-Danlos syndrome, dermatosparaxis type
Ehlers-Danlos syndrome, fibronectinemic type
Ehlers-Danlos syndrome, hypermobility type
Ehlers-Danlos syndrome, vascular-like type
X-linked Ehlers-Danlos syndrome
Joint laxity, familial

Rare disease

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