LD28.10 Ehlers-Danlos syndrome, classical type
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
Ehlers-Danlos syndrome, classic type is a type of Ehlers-Danlos syndromes (EDS), a heterogeneous group of hereditary connective tissue diseases characterised by joint hyperlaxity, cutaneous hyperelasticity and tissue fragility, and is characterised by the following major clinical diagnostic criteria: hyperextensible skin, atrophic cutaneous scars due to tissue fragility and joint hyperlaxity.
postcoordination
Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Has manifestation - multiple selections are allowed
synonyms
- Ehlers-Danlos syndrome, classical type
- Ehlers-Danlos syndrome type 1
- Ehlers-Danlos syndrome type 2
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