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Anterior Segment Dysgenesis (FOXE3)


Genes

FOXE3

Conditions

  • Developmental Eye Disorders
  • Anterior Segment Dysgenesis

Clinical Utility

  • Confirmation of a clinical diagnosis
  • Carrier detection in families with a recessive pattern of inheritance
  • Prenatal diagnosis in at-risk pregnancies

Lab Method

  • Capillary Sequencing
  • Deletion/Duplication Analysis

Test Code

TB10

CPT Codes*

81479x1

ABN Required

No

Turnaround Time**

3 weeks

Preferred Specimen

2-5 mL Blood - Lavender Top Tube

Alternative Specimen

Buccal Swabs

*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.

**Reporting times are typical and begin once the sample(s) are received at the GeneDx laboratory, but could be extended in situations outside GeneDx’s reasonable control.