LD28.1 Ehlers-Danlos syndrome
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2025-01
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 ()
- Ehlers-Danlos syndrome, classical type (LD28.10)
- Other specified types of Ehlers-Danlos syndrome (LD28.1Y)
postcoordination
Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
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