Forms and Documents
Test Details
Expand Genes
ACTA1, ANO5, ASAH1, ATP2A1, B3GALNT2, B4GAT1, BAG3, BICD2, BIN1, BVES, CACNA1S, CAPN3, CAV3, CCDC78, CFL2, CHKB, CLCN1, CNTN1, COL12A1, COL6A1, COL6A2, COL6A3, CRYAB, DAG1, DES, DMD, DNAJB2, DNAJB6, DNM2, DOK7, DPM1, DPM2, DPM3, DYNC1H1, DYSF, EGR2, EMD, FHL1, FKRP, FKTN, FLNC, GAA, GBE1, GMPPB, GNE, IGHMBP2, ISPD, ITGA7, KBTBD13, KLHL40, KLHL41, LAMA2, LAMP2, LARGE, LDB3, LMNA, LMOD3, MEGF10, MICU1, MTM1, MYH2, MYH7, MYOT, NEB, PHKA1, PLEC, PLEKHG5, POMGNT1, POMK, POMT1, POMT2, PYGM, RYR1, SCN4A, SEPN1, SGCA, SGCB, SGCD, SGCG, SIL1, SLC52A2, SLC52A3, SYNE1, TCAP, TMEM5, TNNI2, TNNT1, TNPO3, TOR1AIP1, TPM2, TPM3, TRAPPC11, TRIM32, TRIP4, TRPV4, TTN, UBA1, VCP, VRK1
- Alpha-Dystroglycanopathies
- Becker Muscular Dystrophy (BMD)
- Danon Disease
- Duchenne Muscular Dystrophy (DMD)
- Emery-Dreifuss Muscular Dystrophy (EDMD)
- Hereditary Inclusion Body Myopathy (HIBM)
- Limb-Girdle Muscular Dystrophy (LGMD)
- Muscular Dystrophy-Dystroglycanopathy (LGMD)
- Myofibrillar Myopathy (MFM)
- Myotonia Congenita
- Nemaline Myopathy
- Ullrich CMD/Bethlem Myopathy
- Walker–Warburg Syndrome
- Molecular confirmation of a clinical diagnosis
- Identification of at-risk family members
- Assist with treatment/ management decisions
- Recurrence risk assessment
Ordering
889
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
81407x1, 81408x2, 81161x1, 81405x2, 81406x2, 81404x3
Yes
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.