Audiology & ENT
DNA Labs India | Diagnostic Tests
Audiology & ENT
Clinical Overview
Sub-category mapping under Genetics & Genomics
| Reviewed by: Dr. Rajesh Kumar, MD Pathology | ISO 9001:2015 Certified Laboratory
This content is for educational purposes only. Always consult a qualified healthcare provider for medical advice.
Tests
Connexin 30 Mutation Detection Test
To detect mutations in the GJB6 gene that cause connexin 30-related hearing loss for diagnostic and...
Connexin 26 Mutation Detection Test
To detect mutations in the GJB2 gene associated with Connexin 26-related hearing loss, aiding in the...
COL4A3 Gene Alport syndrome, autosomal recessive NGS Genetic Test
To detect mutations in the COL4A3 gene for diagnosing autosomal recessive Alport Syndrome, aiding in...
PLCB4 Gene Auriculocondylar syndrome type 2 NGS Genetic Test
To detect pathogenic variants in the PLCB4 gene for definitive diagnosis of Auriculocondylar Syndrom...
EYA1 Gene Branchiootic syndrome type 1 NGS Genetic Test
The purpose of the EYA1 Gene Branchiootic Syndrome Type 1 NGS Genetic Test is to identify mutations...
DIAPH3 Gene Auditory neuropathy, autosomal dominant NGS Genetic Test
The purpose of this test is to identify pathogenic mutations in the DIAPH3 gene that cause autosomal...
DIAPH1 Gene Deafness, autosomal dominant type 1 NGS Genetic Test
The purpose of the DIAPH1 Gene Deafness NGS Genetic Test is to diagnose autosomal dominant deafness...
MYO7A Gene Deafness, autosomal dominant type 11 NGS Genetic Test
The purpose of this test is to detect mutations in the MYO7A gene that cause autosomal dominant type...
POU4F3 Gene Deafness, autosomal dominant type 15 NGS Genetic Test
The purpose of this test is to identify mutations in the POU4F3 gene for accurate diagnosis of autos...
COL11A2 Gene Deafness, autosomal dominant type 13 NGS Genetic Test
To diagnose autosomal dominant deafness type 13 (DFNA13) by detecting pathogenic mutations in the CO...
GJB2 Gene Deafness with keratopachydermia and constrictions of fingers and toes NGS Genetic Test
The primary purpose of this test is to identify pathogenic or likely pathogenic mutations in the GJB...
MYH9 Gene Deafness, autosomal dominant type 17 NGS Genetic Test
To identify mutations in the MYH9 gene responsible for autosomal dominant deafness type 17 (DFNA17),...
EYA4 Gene Deafness, autosomal dominant type 10 NGS Genetic Test
To detect mutations in the EYA4 gene associated with autosomal dominant deafness type 10 for diagnos...
TECTA Gene Deafness, autosomal dominant type 12 NGS Genetic Test
The primary purpose of this test is to confirm a molecular diagnosis of autosomal dominant non-syndr...
ACTG1 Gene Deafness, autosomal dominant type 20 NGS Genetic Test
The purpose of this test is to accurately diagnose autosomal dominant type 20 deafness by identifyin...
SIX1 Gene Deafness, autosomal dominant type 23 NGS Genetic Test
The purpose of this test is to detect mutations in the SIX1 gene that cause autosomal dominant type...
MYO6 Gene Deafness, autosomal dominant type 22 NGS Genetic Test
The purpose of this test is to detect mutations in the MYO6 gene that cause autosomal dominant deafn...
KCNQ4 Gene Deafness, autosomal dominant type 2A NGS Genetic Test
The purpose of the KCNQ4 Gene Deafness NGS Genetic Test is to identify mutations in the KCNQ4 gene a...
GJB6 Gene Deafness, autosomal dominant type 3B NGS Genetic Test
The purpose of the GJB6 Gene Deafness NGS Genetic Test is to identify mutations in the GJB6 gene tha...
GRHL2 Gene Deafness, autosomal dominant type 28 NGS Genetic Test
The purpose of the GRHL2 Gene Deafness NGS Genetic Test is to identify pathogenic or likely pathogen...
CRYM Gene Deafness, autosomal dominant type 40 NGS Genetic Test
The purpose of this test is to detect mutations in the CRYM gene to confirm a diagnosis of autosomal...
GJB3 Gene Deafness, autosomal dominant type 2B NGS Genetic Test
To detect pathogenic mutations in the GJB3 gene that cause autosomal dominant deafness type 2B, aidi...
CCDC50 Gene Deafness, autosomal dominant type 44 NGS Genetic Test
The purpose of this test is to detect pathogenic variants in the CCDC50 gene that cause autosomal do...
MYH14 Gene Deafness, autosomal dominant type 4 NGS Genetic Test
To identify mutations in the MYH14 gene that cause autosomal dominant deafness type 4, aiding in dia...
TMC1 Gene Deafness, autosomal dominant type 36 NGS Genetic Test
The purpose of the TMC1 Gene Deafness, Autosomal Dominant Type 36 NGS Genetic Test is to identify pa...
SLC17A8 Gene Deafness, autosomal dominant type 25 NGS Genetic Test
The primary purpose of the SLC17A8 Gene Deafness NGS Genetic Test is to identify pathogenic or likel...
MYO1A Gene Deafness, autosomal dominant type 48 NGS Genetic Test
The purpose of the MYO1A Gene Deafness NGS Genetic Test is to identify mutations in the MYO1A gene r...
CEACAM16 Gene Deafness, autosomal dominant type 4B NGS Genetic Test
To diagnose autosomal dominant type 4B deafness caused by CEACAM16 gene mutations, enabling early in...
GSDME Gene Deafness, autosomal dominant type 5 NGS Genetic Test
The purpose of the GSDME Gene Deafness, Autosomal Dominant Type 5 NGS Genetic Test is to identify mu...
DSPP Gene Deafness, autosomal dominant type 39, with dentinogenesis type 1 NGS Genetic Test
The purpose of this test is to identify pathogenic or likely pathogenic mutations in the DSPP gene t...
TBC1D24 Gene Deafness, autosomal dominant type 65 NGS Genetic Test
The purpose of this test is to detect mutations in the TBC1D24 gene that cause autosomal dominant de...
DIABLO Gene Deafness, autosomal dominant type 64 NGS Genetic Test
To diagnose DIABLO gene mutations causing autosomal dominant deafness type 64, enabling accurate cli...
GJB3 Gene Deafness, autosomal recessive NGS Genetic Test
To identify mutations in the GJB3 gene that cause autosomal recessive deafness, enabling early diagn...
GJB2 Gene Deafness, autosomal dominant type 3A NGS Genetic Test
The primary purpose of this genetic test is to detect pathogenic mutations in the GJB2 gene that are...
WFS1 Gene Deafness, autosomal dominant type 6 NGS Genetic Test
To identify genetic mutations in the WFS1 gene that cause autosomal dominant type 6 deafness, aiding...
CDH23 Gene Deafness, autosomal recessive type 12 NGS Genetic Test
The purpose of the CDH23 Gene Deafness NGS Genetic Test is to accurately diagnose autosomal recessiv...
POU4F3 Gene Deafness, autosomal dominant type 52 NGS Genetic Test
The purpose of this test is to detect pathogenic mutations in the POU4F3 gene that cause autosomal d...
GIPC3 Gene Deafness, autosomal recessive type 15 NGS Genetic Test
Getting tested for GIPC3 gene mutations helps confirm a diagnosis of DFNB15, understand the genetic...
SUN1 Gene Deafness, autosomal recessive NGS Genetic Test
To detect pathogenic mutations in the SUN1 gene for the diagnosis of autosomal recessive deafness an...
GJB2 Gene Deafness, autosomal recessive type 1A NGS Genetic Test
To diagnose GJB2 gene-related autosomal recessive deafness through comprehensive NGS analysis, ident...
COCH Gene Deafness, autosomal dominant type 9 NGS Genetic Test
The COCH Gene Deafness DFNA9 NGS Genetic Test is performed to identify pathogenic mutations in the C...
GJB6 Gene Deafness, autosomal recessive type 1B NGS Genetic Test
The purpose of the GJB6 Gene Deafness NGS Genetic Test is to identify pathogenic mutations in the GJ...
OTOA Gene Deafness, autosomal recessive type 22 NGS Genetic Test
To identify mutations in the OTOA gene associated with autosomal recessive deafness type 22 (DFNB22)...
RDX Gene Deafness, autosomal recessive type 24 NGS Genetic Test
The purpose of this test is to diagnose autosomal recessive deafness type 24 by detecting pathogenic...
MYO7A Gene Deafness, autosomal recessive type 2 NGS Genetic Test
To identify mutations in the MYO7A gene that cause autosomal recessive deafness type 2, aiding in ac...
TRIOBP Gene Deafness, autosomal recessive type 28 NGS Genetic Test
To detect mutations in the TRIOBP gene that cause autosomal recessive deafness type 28, aiding in ac...
GRXCR1 Gene Deafness, autosomal recessive type 25 NGS Genetic Test
The purpose of this test is to diagnose GRXCR1 gene deafness by detecting mutations in the GRXCR1 ge...
PCDH15 Gene Deafness, autosomal recessive type 23 NGS Genetic Test
To identify mutations in the PCDH15 gene that cause autosomal recessive deafness type 23, enabling a...
USH1C Gene Deafness, autosomal recessive type 18 NGS Genetic Test
The purpose of the USH1C Gene Deafness NGS Genetic Test is to identify mutations in the USH1C gene t...
STRC Gene Deafness, autosomal recessive type 16 NGS Genetic Test
This test is performed to identify pathogenic mutations in the STRC gene that cause autosomal recess...
MYO15A Gene Deafness, autosomal recessive type 3 NGS Genetic Test
To identify mutations in the MYO15A gene responsible for autosomal recessive deafness type 3, aiding...
CLDN14 Gene Deafness, autosomal recessive type 29 NGS Genetic Test
To identify mutations in the CLDN14 gene that cause autosomal recessive deafness type 29, aiding in...
MYO3A Gene Deafness, autosomal recessive type 30 NGS Genetic Test
To identify mutations in the MYO3A gene responsible for autosomal recessive deafness type 30, enabli...
ESRRB Gene Deafness, autosomal recessive type 35 NGS Genetic Test
The purpose of the ESRRB Gene Deafness (DFNB35) NGS Genetic Test is to identify pathogenic or likely...
GJB2 Gene Knuckle pads and leukonychia sensorineural deafness NGS Genetic Test
To diagnose GJB2 gene mutations causing sensorineural deafness with associated skin findings like kn...
MYH7B Gene Hearing loss, MYH7B related NGS Genetic Test
To detect mutations in the MYH7B gene that cause hereditary hearing loss, aiding in accurate diagnos...
FLNA Gene Otopaladigital syndrome type 1 NGS Genetic Test
The purpose of the FLNA Gene Otopaladigital Syndrome Type 1 NGS Genetic Test is to identify mutation...
SLC26A4 Gene Pendred syndrome NGS Genetic Test
The purpose of the SLC26A4 Gene Pendred Syndrome NGS Genetic Test is to identify mutations in the SL...
MAP1A Gene Hearing loss, MAP1A related NGS Genetic Test
The purpose of the MAP1A Gene Hearing Loss NGS Genetic Test is to detect pathogenic or likely pathog...
TRMU Gene Mitochondrial modifier of deafness NGS Genetic Test
To identify pathogenic mutations in the TRMU gene associated with mitochondrial modifier of deafness...
COL4A6 Gene Deafness, X-linked type 6 NGS Genetic Test
To identify mutations in the COL4A6 gene responsible for X-linked type 6 deafness, aiding in accurat...
Deafness Gene Panel
The purpose of the Deafness Gene Panel test is to identify genetic mutations responsible for hearing...
ESPN Gene Deafness, autosomal recessive type 36 NGS Genetic Test
The purpose of the ESPN Gene Deafness NGS Genetic Test is to confirm a clinical diagnosis of autosom...
HGF Gene Deafness, autosomal recessive type 39 NGS Genetic Test
To diagnose DFNB39 deafness caused by mutations in the HGF gene through advanced genetic sequencing,...
ILDR1 Gene Deafness, autosomal recessive type 42 NGS Genetic Test
The purpose of this test is to identify mutations in the ILDR1 gene that cause autosomal recessive d...
FOXI1 Gene Deafness, autosomal recessive type 4 NGS Genetic Test
To identify mutations in the FOXI1 gene responsible for autosomal recessive deafness type 4, aiding...
CIB2 Gene Deafness, autosomal recessive type 48 NGS Genetic Test
To identify mutations in the CIB2 gene that cause autosomal recessive deafness type 48, aiding in ac...
MARVELD2 Gene Deafness, autosomal recessive type 49 NGS Genetic Test
The purpose of the MARVELD2 Gene Deafness NGS Genetic Test is to identify mutations in the MARVELD2...
COL11A2 Gene Deafness, autosomal recessive type 53 NGS Genetic Test
To diagnose COL11A2 gene mutations causing autosomal recessive deafness, enabling accurate clinical...
PJVK Gene Deafness, autosomal recessive type 59 NGS Genetic Test
To detect mutations in the PJVK gene associated with autosomal recessive deafness type 59 for accura...
SLC26A5 Gene Deafness, autosomal recessive type 61 NGS Genetic Test
To detect pathogenic mutations in the SLC26A5 gene using next-generation sequencing for the diagnosi...
TMIE Gene Deafness, autosomal recessive type 6 NGS Genetic Test
The purpose of this test is to detect mutations in the TMIE gene that cause autosomal recessive deaf...
LRTOMT Gene Deafness, autosomal recessive type 63 NGS Genetic Test
To identify mutations in the LRTOMT gene responsible for autosomal recessive deafness type 63, aidin...
LHFPL5 Gene Deafness, autosomal recessive type 67 NGS Genetic Test
The purpose of this test is to identify mutations in the LHFPL5 gene using NGS technology for the di...
MSRB3 Gene Deafness, autosomal recessive type 74 NGS Genetic Test
The purpose of the MSRB3 Gene Deafness NGS Genetic Test is to detect pathogenic mutations in the MSR...
PNPT1 Gene Deafness, autosomal recessive type 70 NGS Genetic Test
The purpose of the PNPT1 Gene Deafness NGS Genetic Test is to accurately diagnose mutations in the P...
SYNE4 Gene Deafness, autosomal recessive type 76 NGS Genetic Test
The purpose of the SYNE4 Gene Deafness NGS Genetic Test is to detect mutations in the SYNE4 gene tha...
TMC1 Gene Deafness, autosomal recessive type 7 NGS Genetic Test
The purpose of this test is to diagnose mutations in the TMC1 gene that cause autosomal recessive de...
TMPRSS3 Gene Deafness, autosomal recessive type 8/10 NGS Genetic Test
To detect pathogenic mutations in the TMPRSS3 gene that cause autosomal recessive type 8/10 deafness...
DCDC2 Gene Deafness, autosomal recessive type 66 NGS Genetic Test
To identify pathogenic mutations in the DCDC2 gene associated with autosomal recessive deafness type...
TPRN Gene Deafness, autosomal recessive type 79 NGS Genetic Test
This test helps diagnose TPRN gene-related deafness, providing genetic information for treatment, ma...
TBC1D24 Gene Deafness, autosomal recessive type 86 NGS Genetic Test
The purpose of the TBC1D24 Gene Deafness NGS Genetic Test is to diagnose autosomal recessive type 86...
KARS1 Gene Deafness, autosomal recessive type 89 NGS Genetic Test
The purpose of this test is to identify mutations in the KARS1 gene that cause autosomal recessive d...
OTOF Gene Deafness, autosomal recessive type 9 NGS Genetic Test
To identify mutations in the OTOF gene that cause autosomal recessive deafness type 9, aiding in dia...
SERPINB6 Gene Deafness, autosomal recessive type 91 NGS Genetic Test
The purpose of the SERPINB6 Gene Deafness NGS Genetic Test is to identify mutations in the SERPINB6...
FGF3 Gene Deafness, congenital with inner ear agenesis, microtia, and microdontia NGS Genetic Test
The purpose of this test is to diagnose FGF3 gene mutations responsible for congenital deafness with...
CABP2 Gene Deafness, autosomal recessive type 93 NGS Genetic Test
To diagnose autosomal recessive deafness type 93 caused by mutations in the CABP2 gene, enabling acc...
MT-RNR1 Gene Deafness, nonsyndromic, sensorineural, mitochondrial NGS Genetic Test
To identify pathogenic mutations in the MT-RNR1 gene associated with nonsyndromic sensorineural deaf...
PRPS1 Gene Deafness, X-linked type 1 NGS Genetic Test
To identify mutations in the PRPS1 gene that cause X-linked deafness type 1, aiding in diagnosis, ge...
POU3F4 Gene Deafness, X-linked type 2 NGS Genetic Test
To detect mutations in the POU3F4 gene for definitive diagnosis of X-linked type 2 deafness, enablin...
SMPX Gene Deafness, X-linked type 4 NGS Genetic Test
The purpose of the SMPX Gene Deafness NGS Genetic Test is to identify mutations in the SMPX gene tha...
AIFM1 Gene Deafness, X-linked type 5 NGS Genetic Test
The purpose of this test is to detect mutations in the AIFM1 gene that cause X-linked type 5 deafnes...
DNAAF2 Gene Primary ciliary dyskinesia type 10 NGS Genetic Test
To detect mutations in the DNAAF2 gene for diagnosis of primary ciliary dyskinesia type 10.
CCDC40 Gene Primary ciliary dyskinesia type 15 NGS Genetic Test
The purpose of this test is to diagnose Primary Ciliary Dyskinesia Type 15 by detecting pathogenic m...
DNAAF5 Gene Primary ciliary dyskinesia type 18 NGS Genetic Test
The purpose of this test is to identify mutations in the DNAAF5 gene that cause Primary Ciliary Dysk...
CCNO Gene Primary ciliary dyskinesia type 29 NGS Genetic Test
The purpose of this test is to detect mutations in the CCNO gene and other genes associated with Pri...
NME8 Gene Primary ciliary dyskinesia type 6 NGS Genetic Test
To diagnose Primary Ciliary Dyskinesia Type 6 by identifying mutations in the NME8 gene using NGS te...
DNAI2 Gene Primary ciliary dyskinesia type 9 NGS Genetic Test
To identify pathogenic mutations in the DNAI2 gene for the diagnosis of primary ciliary dyskinesia t...
DNAH9 Gene Primary ciliary dyskinesia, DNAH9 related NGS Genetic Test
The purpose of the DNAH9 Gene NGS Genetic Test is to detect mutations in the DNAH9 gene associated w...
P2RX2 Gene Progressive hearing loss NGS Genetic Test
To identify genetic mutations in the P2RX2 gene that cause progressive hearing loss, aiding in diagn...
SLC26A4 Gene Pendred syndrome NGS Genetic Test
To detect mutations in the SLC26A4 gene for the diagnosis of Pendred syndrome.
Vertebrate Genome De Novo Assembly and Annotation-Illumina
The purpose of vertebrate genome de novo assembly and annotation is to generate a complete and accur...
RNA Extraction from Cultured Cells
The primary purpose of RNA extraction from cultured cells is to obtain pure, intact RNA for various...
RNA Extraction from Bacteria
The primary purpose of RNA extraction from bacteria is to obtain pure, intact RNA for downstream mol...