Nephrotic Syndrome/Focal Segmental Glomerulosclerosis
New York
Approved
Genes
Conditions
- Focal Segmental Glomerulosclerosis
- Alport Syndrome
- Nephrotic Syndrome
- Chronic Kidney Disease Risk
Clinical Utility
- Molecular confirmation of a clinical diagnosis
- Development of appropriate evaluation and management plan
- Evaluation of family members as possible donors for kidney transplantation
- Testing of at-risk relatives for specific known variant(s) previously identified in an affected family member
- Genetic counseling and recurrence risk assessment
Lab Method
- Next-Gen Sequencing
- Deletion/Duplication Analysis
- Capillary Sequencing
Important Information
Test Code
TG99
CPT Codes*
81405x2, 81406x2, 81407x1, 81408x2, 81479x3
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.
**Turnaround times are estimates and begin once the sample(s) begin processing at the GeneDx lab and could be extended in situations outside GeneDx’s control.
Test Documents
Billing
Targeted Variant Testing