Hunter Syndrome

Forms and Documents

Test Details

  • Molecular confirmation of a clinical diagnosis.
  • Molecular diagnosis of patients suspected of having mucopolysaccharidosis type II
  • Prenatal diagnosis for known familial mutation(s) in at-risk pregnancies


4 weeks
2-5 mL Blood - Lavender Top Tube
Buccal Swabs | Extracted DNA

*Reporting times are typical, but could be extended in situations outside GeneDx's reasonable control.


81405x1; 81479x1
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**The CPT codes provided are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.