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LD28.1 Ehlers-Danlos syndrome

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

Ehlers-Danlos syndrome (EDS) is a heterogeneous group of inherited disorders of connective tissue, principally collagen, that range in severity from mild joint hypermobility to life-threatening fragility of soft tissue and vasculature.

sections/codes in this section (LD28.1-LD28.1)

• Ehlers-Danlos syndrome, classical type  (LD28.10)
• Other specified types of Ehlers-Danlos syndrome  (LD28.1Y)

postcoordination

synonyms

• Ehlers-Danlos syndrome
• Cutis hyperelastica
• EDS - [Ehlers-Danlos syndrome]

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