General Reproductive Health
DNA Labs India | Diagnostic Tests
General Reproductive Health
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
FISH - Postnatal Gender Confirmation Test
For evaluating ambiguous genitalia, gender reversal cases, and confirming gender in newborns.
Microarray 60K (POC) + Couple Karyotyping
To diagnose genetic disorders, identify chromosomal abnormalities in couples, and assess causes of i...
Peripheral Blood for High Resolution Couple Karyotyping
The purpose of this test is to detect chromosomal abnormalities in couples experiencing infertility...
Pre-Implantation Genetic Disorder/PGD (Single Embryo)
To check for genetic abnormalities in embryos before implantation during IVF, reducing the risk of p...
Pre-Implantation Genetic Disorder/PGD (Single Embryo) with Maternal DNA Contamination Check
To identify genetic abnormalities in embryos before implantation, reducing the risk of genetic disor...
Pre-Implantation Genetic Disorder/PGD (Single Gene Disorder- Known Mutation)- Baseline
The purpose of PGD for single gene disorders with known mutations is to identify embryos that carry...
Pre-Implantation Genetic Disorder/PGD HLA Typing (Single Embryo)
The purpose of PGD HLA Typing is to identify genetic abnormalities and determine the HLA type of emb...
X & Y Identification Test
The purpose of the X & Y Identification Test is to accurately determine the chromosomal sex of an in...
FMR1 Gene Premature ovarian failure type 1 NGS Genetic Test
To identify mutations in the FMR1 gene that cause premature ovarian failure type 1, enabling accurat...
Infertility panel NGS Genetic Test
The purpose of the Infertility Panel NGS Genetic Test is to diagnose genetic causes of infertility b...
SRY Gene 46,XX sex reversal type 1 NGS Genetic Test
To diagnose mutations in the SRY gene that cause 46,XX sex reversal type 1, aiding in the identifica...
CYP19A1 Gene Aromatase deficiency NGS Genetic Test
To diagnose Aromatase Deficiency by identifying mutations in the CYP19A1 gene, aiding in early manag...
CFTR Gene Congenital bilateral absence of vas deferens NGS Genetic Test
To identify mutations in the CFTR gene that cause Congenital Bilateral Absence of Vas Deferens, aidi...
RXFP2 Gene Cryptorchidism NGS Genetic Test
To diagnose cryptorchidism and identify mutations in the RXFP2 gene, enabling early intervention and...
STRC Gene Deafness and male infertility NGS Genetic Test
To diagnose mutations in the STRC gene associated with deafness and male infertility, enabling early...
FOXF2 Gene Disorders of sex development with cleft palate NGS Genetic Test
To diagnose Disorders of Sex Development with Cleft Palate caused by mutations in the FOXF2 gene usi...
CATSPER2 Gene Deafness and male infertility, CATSPER2 related NGS Genetic Test
To identify mutations in the CATSPER2 gene for the diagnosis of CATSPER2-related deafness and male i...
NLRP7 Gene Hydatidiform mole NGS Genetic Test
The purpose of this test is to diagnose hydatidiform mole and related reproductive disorders by dete...
KHDC3L Gene Hydatidiform mole, recurrent, type 2 NGS Genetic Test
The purpose of the KHDC3L Gene NGS Genetic Test is to identify mutations in the KHDC3L gene that may...
KISS1 Gene Hypogonadotropic hypogonadism NGS Genetic Test
To diagnose KISS1 gene mutations causing hypogonadotropic hypogonadism, enabling early intervention,...
NSMF Gene Hypogonadotropic hypogonadism NGS Genetic Test
The purpose of this test is to diagnose Hypogonadotropic Hypogonadism by detecting mutations in the...
FGF8 Gene Hypogonadotropic hypogonadism type 6 with or without anosmia NGS Genetic Test
The purpose of the FGF8 Gene Hypogonadotropic Hypogonadism Type 6 NGS Genetic Test is to identify mu...
AR Gene Hypospadias type 1, X-linked NGS Genetic Test
The purpose of the AR Gene Hypospadias Type 1 NGS Genetic Test is to identify mutations in the AR ge...
WDR11 Gene Hypogonadtropic hypogonadism type 14 NGS Genetic Test
To identify mutations in the WDR11 gene for the diagnosis of hypogonadotropic hypogonadism type 14,...
MAMLD1 Gene Hypospadias type 2, X-linked NGS Genetic Test
To detect mutations in the MAMLD1 gene associated with hypospadias type 2 for diagnosis, genetic cou...
ZP1 Gene Oocyte maturation defect NGS Genetic Test
To identify genetic mutations in the ZP1 gene that affect oocyte maturation, aiding in the diagnosis...
LHCGR Gene Leydig cell hypoplasia type 1 NGS Genetic Test
The purpose of this test is to identify mutations in the LHCGR gene that cause Leydig cell hypoplasi...
FSHR Gene Ovarian dysgenesis type 1 NGS Genetic Test
The purpose of the FSHR Gene Ovarian Dysgenesis Type 1 NGS Genetic Test is to identify pathogenic mu...
BMP15 Gene Ovarian dysgenesis type 2 NGS Genetic Test
The purpose of the BMP15 Gene Ovarian Dysgenesis Type 2 NGS Genetic Test is to identify mutations in...
AMH Gene Persistent Mullerian duct syndrome type 1 NGS Genetic Test
To diagnose PMDS Type 1 by detecting mutations in the AMH gene using NGS technology, aiding in clini...
C4BPA Gene Pregnancy loss, recurrent, C4BPA related NGS Genetic Test
To identify mutations in the C4BPA gene associated with recurrent pregnancy loss, aiding in diagnosi...
AMHR2 Gene Persistent Mullerian duct syndrome type 2 NGS Genetic Test
To diagnose mutations in the AMHR2 gene causing Persistent Mullerian Duct Syndrome Type 2 (PMDS2), e...
CORIN Gene Preeclampsia/eclampsia type 5 NGS Genetic Test
The purpose of this test is to detect mutations in the CORIN gene that are associated with an increa...
HSD17B3 Gene Pseudohermaphroditism with gynecomastia NGS Genetic Test
To identify mutations in the HSD17B3 gene for definitive diagnosis of pseudohermaphroditism with gyn...
SYCP3 Gene SPGF4 NGS Genetic Test
To identify mutations in the SYCP3 gene associated with primary ovarian insufficiency, infertility,...
AURKC Gene SPGF5 NGS Genetic Test
To identify mutations in the AURKC gene that cause SPGF5 syndrome, enabling accurate diagnosis, gene...
CATSPER1 Gene SPGF7 NGS Genetic Test
To detect mutations in the CATSPER1 gene that cause SPGF7, a genetic disorder leading to male infert...
SPATA16 Gene SPGF6 NGS Genetic Test
The purpose of the SPATA16 Gene SPGF6 NGS Genetic Test is to diagnose genetic mutations in the SPATA...
GATA4 Gene Testicular anomalies with or without congenital heart disease NGS Genetic Test
To detect mutations in the GATA4 gene that cause testicular anomalies and congenital heart disease,...
DPY19L2 Gene SPGF9 NGS Genetic Test
The purpose of the DPY19L2 Gene SPGF9 NGS Genetic Test is to diagnose globozoospermia and identify g...
NR5A1 Gene SPGF8 NGS Genetic Test
The purpose of the NR5A1 Gene SPGF8 NGS Genetic Test is to identify pathogenic or likely pathogenic...
LAMC1 Gene Pelvic organ prolapse, LAMC1 related NGS Genetic Test
The purpose of this test is to detect mutations in the LAMC1 gene that are associated with an increa...
Beta Thalassemia-HBB Full Gene Analysis (Couple)
The purpose of this test is to determine whether either partner carries a mutation in the HBB gene t...
Microarray 60K (POC)
The primary purpose of Microarray 60K (POC) is to identify chromosomal imbalances (CNVs) in products...
IVF Surrogacy Sperm Paternity Test
The primary purpose of the IVF Surrogacy Sperm Paternity Test is to confirm the biological father of...
Carrier Screening
The primary purpose of carrier screening is to identify individuals who carry a gene mutation for an...