Forms and Documents
Test Details
Expand Genes
AKT3, BRWD3, CCND2, CHD8, CUL4B, DNMT3A, EZH2, GLI3, GPC3, HEPACAM, HERC1, MED12, MTOR, NFIA, NFIX, NSD1, OFD1, PHF6, PIK3CA, PIK3R2, PPP2R5D, PTCH1, PTEN, RAB39B, RNF135, SETD2, SNX14, TBC1D7, UPF3B
- Bannayan-Riley-Ruvalcaba Syndrome
- Cowden Syndrome
- FG syndrome
- Gorlin Syndrome
- Greig Cephalopolysyndactyly Syndrome
- Lujan syndrome (LS) (Lujan-Fyns syndrome)
- Macrocephaly
- Non syndromic X-linked ID
- Pallister Hall syndrome (PHS)
- PTEN associated Macrocephaly/Autism Syndrome
- Simpson-Golabi-Behmel Syndrome (SGBS)
- Sotos Syndrome
- Molecular confirmation of a clinical diagnosis
- Identification of at-risk family members
- Assist with treatment/ management decisions
- Recurrence risk assessment
Ordering
699
4 weeks
2-5 mL Blood - Lavender Top Tube
Buccal Swabs
*Reporting times are typical, but could be extended in situations outside GeneDx's reasonable control.
Billing
81321x1, 81323x1, 81401x1, 81405x1, 81406x1
No
Yes
For price inquiries please email zebras@genedx.com
**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.
**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.