Usher Syndrome Panel
New York
Approved
Genes
Conditions
- Usher Syndrome
- Usher Syndrome Type 1/ DFNB12
- Usher Syndrome Type 1J/ DFNB48
- Usher Syndrome Type 3A/ Retinitis Pigmentosa
- Usher type 2C
- Usher Type 1C / DFNA18
- Usher Type 1G
- Usher Type 2A
- Usher Type 2D / DFNB31
- Unspecified Hearing Loss
Clinical Utility
- Congenital deafness and/or moderate to severe hearing loss Problems with balance
- Decreased night vision
- Retinitis pigmentosa
Lab Method
- Next-Gen Sequencing
- Deletion/Duplication Analysis
Test Code
T006
CPT Codes*
81404x2; 81407x1; 81408x2
ABN Required
No
Turnaround Time**
4 weeks
Preferred Specimen
Alternative Specimen
*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.
Test Documents
Billing
Targeted Variant Testing