Hypermobile Ehlers-Danlos syndrome

This code identifies a specific type of Ehlers-Danlos syndrome (EDS) characterized primarily by generalized joint hypermobility, often accompanied by chronic pain, fatigue, and other systemic manifestations. It is a heritable connective tissue disorder affecting collagen structure and function, leading to tissue fragility and widespread symptoms.

Use this code for patients diagnosed with hypermobile Ehlers-Danlos syndrome (hEDS) based on established diagnostic criteria, such as the 2017 International Classification for EDS. Documentation should clearly indicate a clinical diagnosis of hEDS, often supported by a detailed history, physical examination findings (e.g., Beighton score), and exclusion of other EDS types.

• Differentiate from other EDS types (e.g., classical, vascular) which have distinct ICD-10-CM codes.
• Always review documentation for specific EDS type as "Ehlers-Danlos syndrome, unspecified" (Q79.60) is less specific.
• Code all associated manifestations and complications (e.g., chronic pain, dysautonomia, gastrointestinal issues) in addition to the hEDS diagnosis.