General Nephrology & Urology
DNA Labs India | Diagnostic Tests
General Nephrology & Urology
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
Amyloid Protein Identification Test
The purpose of the Amyloid Protein Identification Test is to identify and diagnose amyloid protein d...
CLCNKB Gene Bartter syndrome type 3 NGS Genetic Test
To diagnose Bartter syndrome type 3 by detecting mutations in the CLCNKB gene using NGS technology.
SLC12A7 Gene Bartter syndrome NGS Genetic Test
To confirm the diagnosis of Bartter syndrome by identifying mutations in the SLC12A7 gene and other...
SLC12A5 Gene Bartter syndrome NGS Genetic Test
To detect mutations in the SLC12A5 gene associated with Bartter syndrome for accurate diagnosis and...
SLC12A2 Gene Bartter syndrome NGS Genetic Test
The purpose of the SLC12A2 Gene Bartter Syndrome NGS Genetic Test is to detect mutations in the SLC1...
KCNJ1 Gene Bartter syndrome type 2 NGS Genetic Test
To diagnose Bartter Syndrome Type 2 by detecting mutations in the KCNJ1 gene using Next-Generation S...
SLC12A3 Gene Bartter syndrome NGS Genetic Test
The purpose of the SLC12A3 Gene Bartter Syndrome NGS Genetic Test is to diagnose Bartter syndrome ca...
SLC12A1 Gene Bartter syndrome type 1 NGS Genetic Test
To identify pathogenic mutations in the SLC12A1 gene that cause Bartter Syndrome Type 1, aiding in a...
CLCNKA Gene Bartter syndrome type 4b NGS Genetic Test
The purpose of this test is to detect mutations in the CLCNKA gene to diagnose Bartter Syndrome Type...
SLC3A1 Gene Cystinuria NGS Genetic Test
The purpose of the SLC3A1 Gene Cystinuria NGS Genetic Test is to diagnose cystinuria by identifying...
PREPL Gene Cystinuria NGS Genetic Test
To diagnose cystinuria by detecting mutations in the PREPL gene using next-generation sequencing (NG...
CTNS Gene Cystinosis, nephropathic NGS Genetic Test
The purpose of this test is to detect mutations in the CTNS gene responsible for nephropathic cystin...
AQP2 Gene Diabetes insipidus, nephrogenic, autosomal NGS Genetic Test
The purpose of this test is to detect pathogenic mutations in the AQP2 gene that cause nephrogenic d...
SLC7A9 Gene Cystinuria NGS Genetic Test
To identify mutations in the SLC7A9 gene that cause cystinuria, aiding in diagnosis, family planning...
CLCN5 Gene Dent disease NGS Genetic Test
To confirm diagnosis of Dent disease by detecting mutations in the CLCN5 gene using Next-Generation...
SLC2A9 Gene Hypouricemia, renal type 2 NGS Genetic Test
The purpose of this test is to detect mutations in the SLC2A9 gene to diagnose renal type 2 hypouric...
SLC22A12 Gene Hypouricemia, renal type 1 NGS Genetic Test
The purpose of this test is to diagnose SLC22A12 gene mutations causing renal hypouricemia, enabling...
FAN1 Gene Interstitial nephritis karyomegalic NGS Genetic Test
To identify mutations in the FAN1 gene for the diagnosis of karyomegalic interstitial nephritis, ena...
SCNN1G Gene Liddle syndrome NGS Genetic Test
The purpose of the SCNN1G Gene Liddle Syndrome NGS Genetic Test is to identify mutations in the SCNN...
APOE Gene Lipoprotein glomerulopathy NGS Genetic Test
To detect pathogenic mutations in the APOE gene responsible for lipoprotein glomerulopathy, enabling...
XPNPEP3 Gene Nephronophthisis-like nephropathy type 1 NGS Genetic Test
To detect mutations in the XPNPEP3 gene for accurate diagnosis of Nephronophthisis-like nephropathy...
PLCE1 Gene Nephrotic syndrome type 3 NGS Genetic Test
The purpose of the PLCE1 Gene Nephrotic Syndrome Type 3 NGS Genetic Test is to detect mutations in t...
NEK8 Gene Nephronophthisis type 9 NGS Genetic Test
The purpose of the NEK8 Gene Nephronophthisis Type 9 NGS Genetic Test is to diagnose NPHP9 by detect...
NPHS1 Gene Nephrosis, Finnish type NGS Genetic Test
To detect pathogenic mutations in the NPHS1 gene for diagnosis of Finnish type congenital nephrosis.
NPHS2 Gene Nephrotic syndrome NGS Genetic Test
The purpose of this test is to identify mutations in the NPHS2 gene that cause nephrotic syndrome, a...
COQ8B Gene Nephrotic syndrome type 9 NGS Genetic Test
To identify mutations in the COQ8B gene that cause Nephrotic Syndrome Type 9, aiding in diagnosis, g...
ARHGDIA Gene Nephrotic syndrome type 8 NGS Genetic Test
The purpose of the ARHGDIA Gene Nephrotic Syndrome Type 8 NGS Genetic Test is to detect mutations in...
LAMB2 Gene Nephrotic syndrome type 5 NGS Genetic Test
To diagnose mutations in the LAMB2 gene associated with Nephrotic Syndrome Type 5, enabling early in...
GLIS2 Gene Nephronophthisis type 7 NGS Genetic Test
The purpose of this test is to diagnose Nephronophthisis Type 7 (NPHP7) by detecting mutations in th...
NPHS1 Gene Nephrotic syndrome type 2 NGS Genetic Test
The purpose of this test is to identify mutations in the NPHS1 gene that cause nephrotic syndrome ty...
DGKE Gene Nephrotic syndrome type 7 NGS Genetic Test
To detect mutations in the DGKE gene for the diagnosis of Nephrotic Syndrome Type 7.
AGTR1 Gene Renal tubular dysgenesis NGS Genetic Test
To detect mutations in the AGTR1 gene associated with renal tubular dysgenesis and related disorders...
AGT Gene Renal tubular dysgenesis NGS Genetic Test
To diagnose Renal Tubular Dysgenesis by identifying mutations in the AGT gene using NGS technology.
REN Gene Renal tubular dysgenesis NGS Genetic Test
To identify mutations in the REN gene for accurate diagnosis and management of Renal Tubular Dysgene...
SDCCAG8 Gene Senior-Loken syndrome type 7 NGS Genetic Test
To diagnose Senior-Loken Syndrome Type 7 by detecting mutations in the SDCCAG8 gene using Next Gener...
WDR19 Gene Senior-Loken syndrome type 8 NGS Genetic Test
The purpose of the WDR19 Gene Senior-Loken Syndrome Type 8 NGS Genetic Test is to diagnose Senior-Lo...
Polycystic Kidney Disease Gene Panel
The purpose of the Polycystic Kidney Disease Gene Panel test is to detect genetic mutations associat...
EYA1 Gene Branchiootorenal Syndrome Type 1 NGS Genetic Test
The purpose of this test is to identify disease-causing sequence variants in the EYA1 gene that are...
OCRL Gene Dent disease type 2 NGS Genetic Test
The purpose of this test is to identify disease-causing mutations in the OCRL gene in an individual...
Nephrology Panel NGS Genetic Test
To identify genetic mutations linked to kidney disorders for early diagnosis, personalized treatment...
Atypical hemolytic uremic syndrome Panel NGS Genetic Test
The purpose of this test is to detect genetic mutations in complement-related genes that cause atypi...
COL4A3 Gene Alport syndrome, autosomal recessive NGS Genetic Test
The purpose of this test is to identify pathogenic mutations in the COL4A3 gene to diagnose autosoma...
COL4A4 Gene Alport syndrome, autosomal recessive NGS Genetic Test
To identify mutations in the COL4A4 gene for accurate diagnosis of autosomal recessive Alport syndro...
COL4A5 Gene Alport syndrome, X-Linked NGS Genetic Test
To identify mutations in the COL4A5 gene for the diagnosis of Alport syndrome, guiding treatment and...
SLC34A1 Gene Fanconi renotubular syndrome type 2 NGS Genetic Test
To detect mutations in the SLC34A1 gene for accurate diagnosis of Fanconi Renotubular Syndrome Type...
ACTN4 Gene Focal segmental glomerulosclerosis type 1 NGS Genetic Test
The purpose of this test is to identify pathogenic mutations in the ACTN4 gene associated with Focal...
TRPC6 Gene Focal segmental glomerulosclerosis type 2 NGS Genetic Test
To detect mutations in the TRPC6 gene for the diagnosis of Focal Segmental Glomerulosclerosis Type 2...
CD2AP Gene Focal segmental glomerulosclerosis type 3 NGS Genetic Test
To diagnose Focal segmental glomerulosclerosis type 3 caused by mutations in the CD2AP gene, guide t...
APOL1 Gene Focal segmental glomerulosclerosis type 4, susceptibility to NGS Genetic Test
To detect mutations in the APOL1 gene that increase susceptibility to Focal Segmental Glomeruloscler...
MYO1E Gene Focal segmental glomerulosclerosis type 6 NGS Genetic Test
To identify mutations in the MYO1E gene associated with Focal Segmental Glomerulosclerosis Type 6 fo...
INF2 Gene Focal segmental glomerulosclerosis type 5 NGS Genetic Test
To identify mutations in the INF2 gene that cause Focal Segmental Glomerulosclerosis Type 5, aiding...
PAX2 Gene Focal segmental glomerulosclerosis type 7 NGS Genetic Test
The purpose of this test is to identify mutations in the PAX2 gene associated with Focal Segmental G...
LAMA5 Gene Focal segmental glomerulosclerosis, LAMA5 related NGS Genetic Test
To identify mutations in the LAMA5 gene associated with Focal Segmental Glomerulosclerosis, enabling...
CRB2 Gene Focal segmental glomerulosclerosis type 9 NGS Genetic Test
To identify mutations in the CRB2 gene that cause Focal Segmental Glomerulosclerosis Type 9, aiding...
ANLN Gene Focal segmental glomerulosclerosis type 8 NGS Genetic Test
The purpose of the ANLN Gene FSGS Type 8 NGS Genetic Test is to diagnose Focal Segmental Glomerulosc...
SLC12A3 Gene Gitelman syndrome NGS Genetic Test
To identify mutations in the SLC12A3 gene for diagnosis of Gitelman syndrome.
UMOD Gene Glomerulocystic kidney disease with hyperuricemia and isosthenuria NGS Genetic Test
To diagnose UMOD gene mutations causing glomerulocystic kidney disease with hyperuricemia and isosth...
CFB Gene Hemolytic uremic syndrome NGS Genetic Test
The purpose of the CFB Gene Hemolytic Uremic Syndrome NGS Genetic Test is to diagnose mutations in t...
CFHR1 Gene Hemolytic uremic syndrome NGS Genetic Test
To diagnose Hemolytic Uremic Syndrome caused by mutations in the CFHR1 gene using NGS technology.
CFH Gene Hemolytic uremic syndrome NGS Genetic Test
To identify genetic mutations in the CFH gene associated with Hemolytic Uremic Syndrome (HUS), aidin...
CFHR2 Gene Hemolytic uremic syndrome NGS Genetic Test
To identify mutations or variants in the CFHR2 gene that may cause or increase the risk of Hemolytic...
CFHR3 Gene Hemolytic uremic syndrome NGS Genetic Test
The purpose of the CFHR3 Gene HUS NGS Genetic Test is to detect mutations in the CFHR3 gene that may...
CFHR4 Gene Hemolytic uremic syndrome NGS Genetic Test
To identify mutations in the CFHR4 gene associated with Hemolytic Uremic Syndrome (HUS), aiding in d...
CFHR5 Gene Hemolytic uremic syndrome NGS Genetic Test
To diagnose genetic mutations in the CFHR5 gene that cause atypical Hemolytic Uremic Syndrome (HUS),...
THBD Gene Hemolytic uremic syndrome NGS Genetic Test
To detect mutations in the THBD gene associated with hemolytic uremic syndrome, aiding in early diag...
CD46 Gene Hemolytic uremic syndrome, atypical type 2, susceptibility to NGS Genetic Test
To identify mutations in the CD46 gene for diagnosing susceptibility to atypical hemolytic uremic sy...
CFI Gene Hemolytic uremic syndrome NGS Genetic Test
The purpose of the CFI Gene HUS NGS Genetic Test is to detect mutations in the CFI gene responsible...
UMOD Gene Hyperuricemic nephropathy, familial juvenile type 1 NGS Genetic Test
The purpose of this test is to identify mutations in the UMOD gene that cause hyperuricemic nephropa...
UMOD Gene Medullary cystic kidney disease type 2 NGS Genetic Test
To diagnose Medullary Cystic Kidney Disease Type 2 by detecting mutations in the UMOD gene using NGS...
AVPR2 Gene Nephrogenic syndrome of inapproriate antidiuresis NGS Genetic Test
To diagnose mutations in the AVPR2 gene associated with Nephrogenic Syndrome of Inappropriate Antidi...
CLCN5 Gene Nephrolithiasis type 1 NGS Genetic Test
The purpose of the CLCN5 Gene Nephrolithiasis Type 1 NGS Genetic Test is to detect mutations in the...
TTC21B Gene Nephronophthisis type 12 NGS Genetic Test
To identify mutations in the TTC21B gene for diagnosis of nephronophthisis type 12.
NPHP1 Gene Nephronophthisis type 1 NGS Genetic Test
The purpose of this test is to identify mutations in the NPHP1 gene to diagnose Nephronophthisis typ...
ZNF423 Gene Nephronophthisis type 14 NGS Genetic Test
To identify mutations in the ZNF423 gene associated with Nephronophthisis type 14 for accurate diagn...
WDR19 Gene Nephronophthisis type 13 NGS Genetic Test
To detect pathogenic mutations in the WDR19 gene for the diagnosis of Nephronophthisis type 13, a ra...
CEP164 Gene Nephronophthisis type 15 NGS Genetic Test
To diagnose Nephronophthisis type 15 by detecting pathogenic mutations in the CEP164 gene using Next...
INVS Gene Nephronophthisis type 2 NGS Genetic Test
To diagnose Nephronophthisis type 2 by identifying genetic mutations in the INVS gene using NGS tech...
ANKS6 Gene Nephronophthisis type 16 NGS Genetic Test
The purpose of the ANKS6 Gene Nephronophthisis Type 16 NGS Genetic Test is to identify mutations in...
NPHP4 Gene Nephronophthisis type 4 NGS Genetic Test
The purpose of the NPHP4 Gene Nephronophthisis Type 4 NGS Genetic Test is to identify mutations in t...
DCDC2 Gene Nephronophthisis type 19 NGS Genetic Test
To identify pathogenic mutations in the DCDC2 gene for the diagnosis of Nephronophthisis type 19, en...
NPHP3 Gene Nephronophthisis type 3 NGS Genetic Test
To diagnose Nephronophthisis type 3 by detecting pathogenic mutations in the NPHP3 gene using next-g...
PKHD1 Gene Polycystic kidney and hepatic disease NGS Genetic Test
The purpose of the PKHD1 Gene Polycystic Kidney and Hepatic Disease NGS Genetic Test is to accuratel...
PKHD1 Gene Polycystic kidney disease type 1, autosomal recessive NGS Genetic Test
The PKHD1 Gene Polycystic Kidney Disease Type 1 NGS Genetic Test is designed to identify mutations i...
PKD2 Gene Polycystic kidney disease type 2, autosomal dominant NGS Genetic Test
The purpose of this test is to detect mutations in the PKD2 gene to confirm a diagnosis of autosomal...
PKD1 Gene Polycystic kidney disease type 1, autosomal dominant NGS Genetic Test
The purpose of the PKD1 Gene Polycystic Kidney Disease Type 1 NGS Genetic Test is to detect mutation...
CLCN5 Gene Proteinuria, low molecular weight, with hypercalciuric nephrocalcinosis NGS Genetic Test
To identify mutations in the CLCN5 gene that cause proteinuria, low molecular weight proteinuria, an...
SCNN1B Gene Pseudohypoaldosteronism, type 1, autosomal recessive NGS Genetic Test
The purpose of this test is to detect mutations in the SCNN1B gene to confirm a diagnosis of autosom...
SCNN1G Gene Pseudohypoaldosteronism, type 1, autosomal recessive NGS Genetic Test
To diagnose SCNN1G gene mutations for pseudohypoaldosteronism type 1, enabling accurate clinical man...
BICC1 Gene Renal cystic dysplasia, cystic, susceptibility to NGS Genetic Test
The purpose of this test is to identify mutations in the BICC1 gene that increase susceptibility to...
SLC26A1 Gene Renal dysfunction due to SLC26A1 deficiency NGS Genetic Test
The purpose of this test is to diagnose renal dysfunction caused by SLC26A1 gene deficiency through...
SLC5A2 Gene Renal glucosuria NGS Genetic Test
To diagnose renal glucosuria caused by mutations in the SLC5A2 gene using next-generation sequencing...
ACE Gene Renal tubular dysgenesis NGS Genetic Test
To detect mutations in the ACE gene associated with renal tubular dysgenesis for accurate diagnosis,...
ATP6V1B1 Gene Renal tubular acidosis with deafness NGS Genetic Test
To diagnose Renal Tubular Acidosis with Deafness caused by ATP6V1B1 gene mutations, identify carrier...
SLC4A5 Gene Renal tubular acidosis, SLC4A5 related NGS Genetic Test
To identify mutations in the SLC4A5 gene associated with renal tubular acidosis, aiding in diagnosis...
ATP6V0A4 Gene Renal tubular acidosis, distal, autosomal recessive NGS Genetic Test
To detect mutations in the ATP6V0A4 gene that cause distal renal tubular acidosis, aiding in diagnos...
ROBO2 Gene Vesicoureteral reflux type 2 NGS Genetic Test
To identify genetic mutations in the ROBO2 gene that increase the risk of Vesicoureteral Reflux Type...
SLC4A4 Gene Renal tubular acidosis, proximal, with ocular abnormalities NGS Genetic Test
The purpose of this test is to identify mutations in the SLC4A4 gene that cause proximal renal tubul...
SOX17 Gene Vesicoureteral reflux type 3 NGS Genetic Test
To identify genetic mutations in the SOX17 gene that cause Vesicoureteral Reflux Type 3, aiding in d...
AR Gene Hypospadias type 1, X-linked NGS Genetic Test
The purpose of this NGS genetic test is to identify mutations in the AR gene that cause X-linked hyp...
MAMLD1 Gene Hypospadias type 2, X-linked NGS Genetic Test
The purpose of this test is to detect mutations in the MAMLD1 gene that are associated with X-linked...