Sensory Genetics
DNA Labs India | Diagnostic Tests
Sensory Genetics
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
Nx Gen Sequencing: Usher Syndrome Test
To diagnose Usher syndrome by identifying genetic mutations in associated genes using next-generatio...
Nx Gen Sequencing: Retinitis Pigmentosa Test
The purpose of the Nx Gen Sequencing: Retinitis Pigmentosa Test is to identify pathogenic or likely...
PDE6H Gene Achromatopsia Type 6 NGS Genetic Test
The primary purpose of the PDE6H Gene Achromatopsia Type 6 NGS Genetic Test is to identify pathogeni...
CACNA1F Gene Aland Island Eye Disease NGS Genetic Test
To diagnose Aland Island Eye Disease by identifying pathogenic mutations in the CACNA1F gene through...
TGFBI Gene Corneal Dystrophy, Epithelial Basement Membrane NGS Genetic Test
The primary purpose of the TGFBI Gene Corneal Dystrophy NGS Genetic Test is to identify pathogenic o...
ADAMTSL4 Gene Ectopia Lentis Et Pupillae NGS Genetic Test
The purpose of the ADAMTSL4 Gene Ectopia Lentis et Pupillae NGS Genetic Test is to identify pathogen...
TSPAN12 Gene Exudative Vitreoretinopathy Type 5 NGS Genetic Test
The primary purpose of the TSPAN12 Gene EVR Type 5 NGS Genetic Test is to identify pathogenic or lik...
IARS2 Gene Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia NGS Genetic Test
The purpose of the IARS2 Gene NGS Genetic Test is to identify pathogenic mutations in the IARS2 gene...
WHRN Gene Deafness, autosomal recessive type 31 NGS Genetic Test
The purpose of the WHRN Gene Deafness Type 31 NGS Genetic Test is to identify pathogenic or likely p...
GJB2 Gene Keratoderma, palmoplantar, with deafness NGS Genetic Test
The primary purpose of this test is to identify pathogenic or likely pathogenic mutations in the GJB...
TYRP1 Gene Albinism, Oculocutaneous Type 3 NGS Genetic Test
The purpose of this NGS genetic test is to identify pathogenic sequence variants in the TYRP1 gene t...
CEP290 Gene Bardet-Biedl Syndrome Type 14 NGS Genetic Test
The purpose of this test is to detect disease-causing variants in the CEP290 gene associated with Ba...
WFS1 Gene Cataract Type 41 NGS Genetic Test
The purpose of this NGS genetic test is to identify a clinically significant variant in the WFS1 gen...
CRYAB Gene Cataract, Posterior Polar Type 2 NGS Genetic Test
To confirm a clinical diagnosis of posterior polar cataract type 2 due to CRYAB gene mutations, iden...
NHS Gene Cataract, X-Linked NGS Genetic Test
The purpose of this test is to identify pathogenic mutations in the NHS gene associated with X-linke...
CACNA1F Gene Cone-Rod Dystrophy, X-Linked Type 3 NGS Genetic Test
The primary purpose of this test is to identify pathogenic variants in the CACNA1F gene to confirm a...
LOXHD1 Gene Deafness, autosomal recessive type 77 NGS Genetic Test
The purpose of the LOXHD1 Gene Deafness autosomal recessive type 77 NGS Genetic Test is to identify...
LAMB3 Gene Amelogenesis imperfecta type 1A NGS Genetic Test
To identify mutations in the LAMB3 gene that cause Amelogenesis Imperfecta Type 1A, enabling accurat...
ENAM Gene Amelogenesis imperfecta type 1C NGS Genetic Test
To diagnose amelogenesis imperfecta type 1C by detecting pathogenic mutations in the ENAM gene using...
AMELX Gene Amelogenesis imperfecta type 1E NGS Genetic Test
To identify pathogenic mutations in the AMELX gene for diagnosis of Amelogenesis Imperfecta Type 1E,...
FAM20A Gene Amelogenesis imperfecta type 1G NGS Genetic Test
The purpose of this test is to identify mutations in the FAM20A gene to diagnose amelogenesis imperf...
KLK4 Gene Amelogenesis imperfecta type 2A1 NGS Genetic Test
To identify mutations in the KLK4 gene for accurate diagnosis of Amelogenesis Imperfecta Type 2A1, e...
WDR72 Gene Amelogenesis imperfecta type 2A3 NGS Genetic Test
The purpose of this test is to identify mutations in the WDR72 gene that cause Amelogenesis Imperfec...
DLX3 Gene Amelogenesis imperfecta type 4 NGS Genetic Test
The purpose of the DLX3 Gene Amelogenesis Imperfecta Type 4 NGS Genetic Test is to identify mutation...
DSPP Gene Dentin dysplasia, type 2 NGS Genetic Test
To identify mutations in the DSPP gene for definitive diagnosis of dentin dysplasia type 2, enabling...
DSPP Gene Dentinogenesis imperfecta, Shields type 2 NGS Genetic Test
To identify mutations in the DSPP gene that cause Dentinogenesis Imperfecta Shields type 2, aiding i...
TUFT1 Gene Tuftelin deficiency NGS Genetic Test
To identify mutations in the TUFT1 gene associated with tuftelin deficiency and tooth enamel defects...