Happy holidays! Please be advised that in-transit patient samples will be held by the carrier on Dec. 25 and received by our lab the next day. Kit orders placed on Dec. 25 will be sent on Dec. 26. Our genetic counseling services, client services, and billing services will be unavailable Dec. 24-25; please leave us a message at 888-729-1206 or [email protected] and we will respond when we return.

Hearing Loss Panel

New York
Approved

Genes

ABHD12, ACTB, ACTG1, ADCY1, ADGRV1 (GPR98), AIFM1, ALMS1, ANKH, ATP6V1B1, BDP1, BSND, CABP2, CACNA1D, CCDC50, CD164, CDC14A, CDH23, CEACAM16, CHD7, CIB2, CLDN14, CLIC5, CLPP, CLRN1, COCH, COL11A1, COL11A2, COL2A1, COL4A3, COL4A4, COL4A5, COL4A6, CRYM, DCDC2, DFNA5, DFNB59, DIABLO, DIAPH1, DIAPH3, DNMT1, DSPP, EDN3, EDNRB, ELMOD3, EPS8, ESPN, ESRRB, EYA1, EYA4, FGF3, FGFR1, FGFR2, FGFR3, FOXI1, GATA3, GIPC3, GJA1, GJB2(CX26), GJB3(CX31), GJB6(CX30), GPSM2, GRHL2, GRXCR1, HARS, HARS2, HGF, HOMER2, HSD17B4, ILDR1, KARS, KCNE1, KCNJ10, KCNQ1, KCNQ4, KITLG, LARS2, LHFPL5, LRTOMT, MARVELD2, MCM2, MIR96, MITF, MSRB3, MT-CO1, MT-RNR1, MT-TL1, MT-TS1, MYH14, MYH9, MYO15A, MYO3A, MYO6, MYO7A, NDP, NLRP3, OPA1, OSBPL2, OTOA, OTOF, OTOG, OTOGL, P2RX2, PAX3, PCDH15, PDZD7, PMP22, PNPT1, POLR1D, POU3F4, POU4F3, PRPS1, PTPRQ, RDX, RIPOR2, S1PR2, SALL1, SEMA3E, SERPINB6, SIX1, SIX5, SLC17A8, SLC26A4, SLC26A5, SLC33A1, SLITRK6, SMPX, SNAI2, SOX10, SOX2, STRC, SYNE4, TBC1D24, TBX1, TCOF1, TECTA, TFAP2A, TIMM8A, TJP2, TMC1, TMIE, TMPRSS3, TNC, TPRN, TRIOBP, TSPEAR, USH1C, USH1G, USH2A, WFS1, WHRN(DFNB31)

Conditions

  • Alstrom Syndrome
  • Arts Syndrome
  • Branchiooculofacial Syndrome
  • Craniometaphyseal Dysplasia
  • Deafness-Infertility Syndrome
  • Dentinogenesis Imperfecta and Deafness
  • Hereditary Sensory and Autonomic Neuropathy IE (HSAN1E)
  • Jervell and Lange-Nielsen Syndrome
  • Sinoatrial Node Dysfunction and Deafness (SANDD)
  • Charcot Marie Tooth (CMT)
  • CHARGE Syndrome
  • Clouston Syndrome
  • Kallmann Syndrome
  • Keratitis-Ichthyosis-Deafness syndrome (KID syndrome)
  • Alport Syndrome
  • Maternally Inherited Deafness or Aminoglycoside-Induced Deafness
  • Maternally Inherited Diabetes and Deafness (MIDD)
  • Muckle-Wells Syndrome
  • Norrie Disease
  • Pendred Syndrome
  • Sensorineural Hearing Loss (SNHL)
  • Stickler syndrome
  • Townes-Brocks Syndrome
  • Usher Syndrome
  • Vohwinkel syndrome
  • Baraitser-Winter Syndrome
  • Renal tubular acidosis with deafness
  • Bartter Syndrome/ SNHL
  • Usher Syndrome Type 1/ DFNB12
  • Usher Syndrome Type 1J/ DFNB48
  • Perrault Syndrome
  • Usher Syndrome Type 3A/ Retinitis Pigmentosa
  • Non-ocular stickler (STL3) / otospondylomegaepiphyseal dysplasia (OSMED)/ DFNA13/ DFNB53
  • Usher type 2C
  • Chudley-McCullough syndrome
  • Mohr-Tranebjaerg syndrome
  • Usher Type 1C / DFNA18
  • Usher Type 2A
  • Usher Type 2D / DFNB31
  • Deafness and Myopia
  • Syndromic Micropthalmia Type 3
  • Branchiootic Syndrome
  • Branchiootorenal Syndrome
  • Marshall syndrome
  • Craniosynostosis

Clinical Utility

  • Molecular confirmation of a clinical diagnosis
  • To assist with decisions about treatment and management
  • Testing of at-risk relatives for specific known variant(s) previously identified in an affected family member
  • Genetic counseling, especially recurrence risk

Lab Method

  • Next-Gen Sequencing
  • Long Range PCR
  • Sanger/ABI sequencing
  • Deletion/Duplication Analysis

Test Code

J806

CPT Codes*

81430x1, 81431x1

ABN Required

No

Turnaround Time**

4 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.

**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.

Need something else?

Search More Tests