Ehlers-Danlos syndromes (EDS) form a heterogeneous group of hereditary connective tissue diseases characterized by joint hyperlaxity, cutaneous hyperelasticity and tissue fragility.
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Ehlers-Danlos syndrome, classic type
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Ehlers-Danlos syndrome, hypermobility type
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Ehlers-Danlos syndrome, arthrochalasia type
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Ehlers-Danlos syndrome, spondylodysplastic type
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Ehlers-Danlos syndrome, autosomal dominant, type unspecified
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joint laxity, familial
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