Cardiovascular Markers & Disease
DNA Labs India | Diagnostic Tests
Cardiovascular Markers & Disease
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
MMC (Maternal Myopathy with Cardiomyopathy) Mutation Detection Test
The purpose of the MMC Mutation Detection Test is to identify mutations in the TTN gene that cause M...
LPA Gene Coronary artery disease, susceptibility to NGS Genetic Test
The purpose of the LPA Gene Coronary Artery Disease Susceptibility NGS Genetic Test is to identify g...
ITIH4 Gene Hypercholesterolemia, susceptibility to NGS Genetic Test
To identify genetic mutations in the ITIH4 gene associated with susceptibility to hypercholesterolem...
PPP1R17 Gene Hypercholesterolemia, susceptibility to NGS Genetic Test
To identify mutations in the PPP1R17 gene associated with susceptibility to hypercholesterolemia, ai...
APOA1 Gene Hypoalphalipoproteinemia NGS Genetic Test
To detect pathogenic mutations in the APOA1 gene associated with hypoalphalipoproteinemia, enabling...
GJC2 Gene Lymphedema, hereditary, type IC NGS Genetic Test
The purpose of this test is to detect mutations in the GJC2 gene to diagnose hereditary lymphedema t...
RYR2 Gene Arrhythmogenic right ventricular dysplasia type 2 NGS Genetic Test
To identify mutations in the RYR2 gene associated with Arrhythmogenic Right Ventricular Dysplasia Ty...
DSG2 Gene Arrhythmogenic right ventricular cardiomyopathy type 10 NGS Genetic Test
To identify pathogenic mutations in the DSG2 gene associated with arrhythmogenic right ventricular c...
DSP Gene Arrhythmogenic right ventricular cardiomyopathy type 8 NGS Genetic Test
To identify mutations in the DSP gene associated with Arrhythmogenic Right Ventricular Cardiomyopath...
Cardiology Panel NGS Genetic Test
To identify genetic mutations associated with cardiovascular diseases for early diagnosis, risk asse...
TMEM43 Gene Arrhythmogenic right ventricular cardiomyopathy type 5 NGS Genetic Test
The purpose of the TMEM43 Gene ARVC5 NGS Genetic Test is to identify mutations in the TMEM43 gene th...
TGFB3 Gene Arrhythmogenic right ventricular cardiomyopathy type 1 NGS Genetic Test
The purpose of the TGFB3 Gene NGS Genetic Test is to identify mutations in the TGFB3 gene that cause...
FOXF1 Gene Alveolar capillary dysplasia with misalignment of pulmonary veins NGS Genetic Test
To detect mutations in the FOXF1 gene for the diagnosis of Alveolar capillary dysplasia with misalig...
PKP2 Gene Arrhythmogenic right ventricular cardiomyopathy type 9 NGS Genetic Test
The purpose of this test is to detect mutations in the PKP2 gene associated with Arrhythmogenic Righ...
JUP Gene Arrhythmogenic right ventricular cardiomyopathy type 12 NGS Genetic Test
The purpose of the JUP Gene ARVC Type 12 NGS Genetic Test is to identify mutations in the JUP gene t...
NPPA Gene Atrial fibrillation type 6 NGS Genetic Test
To identify mutations in the NPPA gene associated with atrial fibrillation type 6, aiding in early d...
KCNQ1 Gene Atrial fibrillation type 3 NGS Genetic Test
The purpose of the KCNQ1 Gene Atrial Fibrillation Type 3 NGS Genetic Test is to detect mutations in...
CNOT3 Gene Cardiac defects, CNOT3 related NGS Genetic Test
To identify mutations in the CNOT3 gene associated with cardiac defects for early diagnosis and mana...
PPP1R8 Gene Cardiac defects, PPP1R8 related NGS Genetic Test
The purpose of this test is to detect pathogenic mutations in the PPP1R8 gene that are linked to car...
FLNA Gene Cardiac valvular dysplesia, X-linked NGS Genetic Test
To identify mutations in the FLNA gene that cause cardiac valvular dysplasia, enabling accurate diag...
SCO2 Gene Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency NGS Genetic Test
To identify mutations in the SCO2 gene responsible for cardioencephalomyopathy, aiding in diagnosis,...
CAV3 Gene Cardiomyopathy, familial hypertrophic NGS Genetic Test
To detect mutations in the CAV3 gene that cause familial hypertrophic cardiomyopathy, aiding in diag...
MYL2 Gene Cardiomyopathy, familial hypertrophic type 10 NGS Genetic Test
The purpose of the MYL2 Gene Cardiomyopathy NGS Genetic Test is to identify mutations in the MYL2 ge...
MYOZ2 Gene Cardiomyopathy, familial hypertrophic type 16 NGS Genetic Test
To diagnose MYOZ2 gene-related familial hypertrophic cardiomyopathy through genetic sequencing, aidi...
DSP Gene Cardiomyopathy, dilated with woolly hair and keratoderma NGS Genetic Test
To detect mutations in the DSP gene associated with dilated cardiomyopathy, woolly hair, and keratod...
DNAJC19 Gene Cardiomyopathy, dilated with ataxia NGS Genetic Test
To identify mutations in the DNAJC19 gene for diagnosis of dilated cardiomyopathy with ataxia.
TNNT2 Gene Cardiomyopathy, familial hypertrophic type 2 NGS Genetic Test
To detect mutations in the TNNT2 gene associated with familial hypertrophic cardiomyopathy for diagn...
CALR3 Gene Cardiomyopathy, familial hypertrophic type 19 NGS Genetic Test
To identify mutations in the CALR3 gene associated with familial hypertrophic cardiomyopathy type 19...
LMNA Gene Cardiomyopathy, dilated with hypergonadotropic hypogonadism NGS Genetic Test
The purpose of this test is to identify mutations in the LMNA gene that cause dilated cardiomyopathy...
GATAD1 Gene Cardiomyopathy, dilated type 2B NGS Genetic Test
The purpose of this test is to identify mutations in the GATAD1 gene that cause dilated cardiomyopat...
CAV3 Gene Long QT syndrome type 9 NGS Genetic Test
The purpose of this test is to identify pathogenic mutations in the CAV3 gene associated with Long Q...
ANK2 Gene Long QT syndrome type 4 NGS Genetic Test
The purpose of the ANK2 Gene Long QT Syndrome Type 4 NGS Genetic Test is to detect mutations in the...
KCNE2 Gene Long QT syndrome type 6 NGS Genetic Test
To identify pathogenic variants in the KCNE2 gene associated with Long QT Syndrome Type 6 for accura...
MT-TL1 Gene MELAS syndrome, MT-TL1 related NGS Genetic Test
To diagnose MELAS syndrome by detecting mutations in the MT-TL1 gene using Next-Generation Sequencin...
SCN5A Gene Long QT syndrome type 3 NGS Genetic Test
The purpose of the SCN5A Gene Long QT Syndrome Type 3 NGS Genetic Test is to accurately diagnose Lon...
FBN1 Gene MASS syndrome NGS Genetic Test
To detect mutations in the FBN1 gene associated with MASS syndrome and related connective tissue dis...
CACNA1C Gene Long QT syndrome type 8 NGS Genetic Test
To identify mutations in the CACNA1C gene that cause Long QT Syndrome Type 8, enabling early diagnos...
KCNH2 Gene Long QT syndrome type 2 NGS Genetic Test
To diagnose Long QT syndrome type 2 by detecting pathogenic mutations in the KCNH2 gene using NGS te...
TGFBR1 Gene Aortic aneurysm, familial thoracic type 5 NGS Genetic Test
To identify pathogenic mutations in the TGFBR1 gene that cause familial thoracic aortic aneurysm typ...
ABCC6 Gene Arterial calcification type 2, generalized, infantile NGS Genetic Test
To identify mutations in the ABCC6 gene for diagnosis of Arterial calcification type 2, generalized,...
PRKG1 Gene Aortic aneurysm, familial thoracic type 8 NGS Genetic Test
The purpose of this test is to detect mutations in the PRKG1 gene associated with familial thoracic...
SLC2A10 Gene Arterial Tortuosity Syndrome NGS Genetic Test
The purpose of the SLC2A10 Gene Arterial Tortuosity Syndrome NGS Genetic Test is to identify pathoge...
MYH11 Gene Aortic aneurysm, familial thoracic type 4 NGS Genetic Test
To detect mutations in the MYH11 gene for early diagnosis, risk assessment, and management of famili...
MYLK Gene Aortic aneurysm, familial thoracic type 7 NGS Genetic Test
To identify pathogenic mutations in the MYLK gene that increase the risk of familial thoracic aortic...
SOAT1 Gene Atherosclerosis, SOAT1 related NGS Genetic Test
To identify mutations in the SOAT1 gene associated with an increased risk of atherosclerosis, aiding...
TGFBR2 Gene Aortic aneurysm, familial thoracic type 3 NGS Genetic Test
The purpose of the TGFBR2 Gene Aortic Aneurysm NGS Genetic Test is to identify mutations in the TGFB...
ACTA2 Gene Aortic aneurysm, familial thoracic type 6 NGS Genetic Test
To identify genetic mutations in the ACTA2 gene associated with familial thoracic aortic aneurysm an...
SERPINC1 Gene Antithrombin III deficiency NGS Genetic Test
To detect pathogenic mutations in the SERPINC1 gene for diagnosing hereditary antithrombin III defic...
Cardiomyopathy Gene Panel
To identify genetic mutations responsible for cardiomyopathy, aiding in diagnosis, family screening,...
Cardiac Channelopathy Gene Panel
The purpose of the Cardiac Channelopathy Gene Panel is to identify genetic mutations responsible for...
LDB3 Gene Cardiomyopathy, Hypertrophic, Type 24 NGS Genetic Test
This test is used to identify pathogenic variants in the LDB3 gene in individuals with clinical or f...
LDLRAP1 Gene Hypercholesterolemia autosomal recessive NGS Genetic Test
To diagnose autosomal recessive hypercholesterolemia caused by mutations in the LDLRAP1 gene using N...
CACNA1D Gene Sinoatrial node dysfunction and deafness NGS Genetic Test
To identify genetic mutations in the CACNA1D gene that cause sinoatrial node dysfunction and deafnes...
GDF2 Gene Telangiectasia hereditary hemorrhagic type 5 NGS Genetic Test
To diagnose Hereditary Hemorrhagic Telangiectasia Type 5 by detecting mutations in the GDF2 gene usi...
ENG Gene Telangiectasia, hereditary hemorrhagic, of Rendu, Osler and Weber type 1 NGS Genetic Test
The purpose of the ENG Gene Telangiectasia NGS Genetic Test is to confirm a diagnosis of Hereditary...
ACVRL1 Gene Telangiectasia, hereditary hemorrhagic, type 2 NGS Genetic Test
The purpose of this test is to detect mutations in the ACVRL1 gene to confirm a diagnosis of Heredit...
TBX20 Gene Atrial septal defect type 4 NGS Genetic Test
The purpose of this test is to identify mutations in the TBX20 gene that may cause Atrial Septal Def...
ACTC1 Gene Atrial septal defect type 5 NGS Genetic Test
To detect mutations in the ACTC1 gene for accurate diagnosis, management, and genetic counseling of...
GATA6 Gene Atrial septal defect type 9 NGS Genetic Test
To diagnose Atrial Septal Defect Type 9 by detecting mutations in the GATA6 gene using next-generati...
GATA6 Gene Atrioventricular septal defect type 5 NGS Genetic Test
The purpose of this test is to identify pathogenic mutations in the GATA6 gene that cause Atrioventr...
TAZ Gene Barth syndrome NGS Genetic Test
To diagnose Barth Syndrome by identifying mutations in the TAZ gene using NGS technology, enabling a...
SCN5A Gene Brugada syndrome type 1 NGS Genetic Test
The purpose of this test is to confirm the presence of pathogenic mutations in the SCN5A gene, aidin...
GPD1L Gene Brugada syndrome type 2 NGS Genetic Test
To detect mutations in the GPD1L gene associated with Brugada Syndrome Type 2 for accurate diagnosis...
HCN4 Gene Brugada syndrome type 8 NGS Genetic Test
The purpose of the HCN4 Gene Brugada Syndrome Type 8 NGS Genetic Test is to identify pathogenic muta...
MT-ATP8 Gene Cardiomyopathy, apical hypertrophic, and neuropathy, MT-ATP8 related NGS Genetic Test
To detect mutations in the MT-ATP8 gene associated with cardiomyopathy, apical hypertrophic, and neu...
DSG2 Gene Cardiomyopathy, dilated type 1BB NGS Genetic Test
To detect mutations in the DSG2 gene associated with dilated cardiomyopathy type 1BB for diagnosis,...
RBM20 Gene Cardiomyopathy, dilated type 1DD NGS Genetic Test
To diagnose RBM20 gene cardiomyopathy by detecting mutations in the RBM20 gene using next-generation...
TNNT2 Gene Cardiomyopathy, dilated type 1D NGS Genetic Test
To identify mutations in the TNNT2 gene that cause dilated cardiomyopathy type 1D, aiding in diagnos...
LDB3 Gene Cardiomyopathy, dilated type 1C NGS Genetic Test
The purpose of the LDB3 Gene Cardiomyopathy NGS Genetic Test is to detect mutations in the LDB3 gene...
CRYAB Gene Cardiomyopathy, dilated type 1 NGS Genetic Test
To identify mutations in the CRYAB gene that may cause dilated cardiomyopathy type 1, aiding in diag...
SCN5A Gene Cardiomyopathy, dilated type 1E NGS Genetic Test
The purpose of the SCN5A Gene Cardiomyopathy NGS Genetic Test is to identify mutations in the SCN5A...
MYH6 Gene Cardiomyopathy, dilated type 1EE NGS Genetic Test
The purpose of the MYH6 Gene Cardiomyopathy NGS Genetic Test is to identify mutations in the MYH6 ge...
TTN Gene Cardiomyopathy, dilated type 1G NGS Genetic Test
The purpose of this test is to detect mutations in the TTN gene that cause dilated cardiomyopathy ty...
EYA4 Gene Cardiomyopathy, dilated type 1J NGS Genetic Test
The purpose of the EYA4 Gene Cardiomyopathy, dilated type 1J NGS Genetic Test is to detect mutations...
SGCD Gene Cardiomyopathy, dilated type 1L NGS Genetic Test
The purpose of this test is to identify mutations in the SGCD gene that cause dilated cardiomyopathy...
PRDM16 Gene Cardiomyopathy, dilated type 1LL NGS Genetic Test
The purpose of this test is to detect mutations in the PRDM16 gene that cause dilated cardiomyopathy...
TMPO Gene Cardiomyopathy, dilated type 1T NGS Genetic Test
To diagnose TMPO gene mutations causing dilated cardiomyopathy type 1T, aiding in early detection, t...
PLN Gene Cardiomyopathy, dilated type 1P NGS Genetic Test
The purpose of the PLN Gene Cardiomyopathy NGS Genetic Test is to identify mutations in the PLN gene...
FKTN Gene Cardiomyopathy, dilated type 1X NGS Genetic Test
To diagnose dilated cardiomyopathy caused by mutations in the FKTN gene, aiding in early detection,...
TNNC1 Gene Cardiomyopathy, dilated type 1Z NGS Genetic Test
The purpose of the TNNC1 gene cardiomyopathy NGS genetic test is to identify mutations in the TNNC1...
TPM1 Gene Cardiomyopathy, dilated type 1Y NGS Genetic Test
To identify mutations in the TPM1 gene for accurate diagnosis of dilated type 1Y cardiomyopathy, aid...
MYBPC3 Gene Cardiomyopathy, familial hypertrophic type 4 NGS Genetic Test
To identify pathogenic mutations in the MYBPC3 gene that cause familial hypertrophic cardiomyopathy...
TNNI3 Gene Cardiomyopathy, familial hypertrophic type 7 NGS Genetic Test
The purpose of the TNNI3 Gene Cardiomyopathy NGS Genetic Test is to detect mutations in the TNNI3 ge...
TTN Gene Cardiomyopathy, familial hypertrophic type 9 NGS Genetic Test
To detect mutations in the TTN gene associated with familial hypertrophic cardiomyopathy type 9, aid...
MT-TH Gene Cardiomyopathy, idiopathic dilated, mitochondrial, MT-TH related NGS Genetic Test
The purpose of the MT-TH Gene Cardiomyopathy NGS Genetic Test is to detect mutations in the MT-TH ge...
MT-TG Gene Cardiomyopathy, hypertrophic, MT-TG related NGS Genetic Test
The purpose of the MT-TG Gene Cardiomyopathy NGS Genetic Test is to identify mutations in the MT-TG...
PRKD1 Gene Congenital heart defects and ectodermal dysplasia NGS Genetic Test
To detect pathogenic mutations in the PRKD1 gene for accurate diagnosis of congenital heart defects...
GATA5 Gene Congenital heart defects multiple types NGS Genetic Test
To identify mutations in the GATA5 gene for diagnosing congenital heart defects and guiding treatmen...
MYH7B Gene Cardiomyopathy, left ventricular noncompaction, MYH7B related NGS Genetic Test
To detect mutations in the MYH7B gene for diagnosis of left ventricular noncompaction cardiomyopathy...
ZFPM2 Gene Diaphragmatic hernia type 3 NGS Genetic Test
The purpose of this test is to detect mutations in the ZFPM2 gene to confirm a diagnosis of diaphrag...
DBH Gene Dopamine beta-hydroxylase (DBH) deficiency NGS Genetic Test
To identify mutations in the DBH gene causing dopamine beta-hydroxylase deficiency for diagnosis, ca...
LAMP2 Gene Danon disease NGS Genetic Test
The purpose of this test is to identify mutations in the LAMP2 gene that cause Danon disease, enabli...
DSP Gene Dilated cardiomyopathy with woolly hair, keratoderma, and tooth agenesis NGS Genetic Test
To identify mutations in the DSP gene that cause dilated cardiomyopathy with woolly hair, keratoderm...
MYLK2 Gene Cardiomyopathy, hypertrophic, midventricular, digenic NGS Genetic Test
To identify mutations in the MYLK2 gene and associated genes using next-generation sequencing for th...
SCN5A Gene Heart block, progressive, familial, type 1A NGS Genetic Test
To confirm the diagnosis of SCN5A gene-related progressive familial heart block type 1A through iden...
LMNA Gene Heart-hand syndrome, Slovenian type NGS Genetic Test
The purpose of the LMNA Gene Heart-hand Syndrome NGS Genetic Test is to identify pathogenic mutation...
KCNQ1 Gene Jervell and Lange-Nielsen syndrome type 1 NGS Genetic Test
To detect pathogenic mutations in the KCNQ1 gene for diagnosis of Jervell and Lange-Nielsen Syndrome...
DTNA Gene Left ventricular noncompaction 1, with or without congenital heart defects NGS Genetic Test
The purpose of this test is to identify mutations in the DTNA gene that cause left ventricular nonco...
KCNQ1 Gene Long QT syndrome type 1 NGS Genetic Test
The purpose of the KCNQ1 Gene Long QT Syndrome Type 1 NGS Genetic Test is to detect mutations in the...
SNTA1 Gene Long QT syndrome type 12 NGS Genetic Test
The purpose of the SNTA1 Gene Long QT Syndrome Type 12 NGS Genetic Test is to identify mutations in...
SCN4B Gene Long QT syndrome type 10 NGS Genetic Test
To identify mutations in the SCN4B gene associated with Long QT Syndrome Type 10 for accurate diagno...
MT-TS2 Gene MERRF/MELAS overlap syndrome, MT-TS2 related NGS Genetic Test
To diagnose MERRF/MELAS overlap syndrome by detecting mutations in the MT-TS2 gene using advanced NG...
SLC25A3 Gene Mitochondrial phosphate carrier deficiency NGS Genetic Test
To identify mutations in the SLC25A3 gene for the diagnosis of Mitochondrial Phosphate Carrier Defic...
MT-TQ Gene Myopathy, MT-TQ related NGS Genetic Test
To diagnose MT-TQ gene myopathy by identifying mutations in the MT-TQ gene using next-generation seq...
TRPM4 Gene Progressive familial heart block NGS Genetic Test
To diagnose progressive familial heart block by detecting mutations in the TRPM4 gene, aiding in cli...
GATA6 Gene Pancreatic agenesis and congenital heart defects NGS Genetic Test
To identify mutations in the GATA6 gene that cause pancreatic agenesis and congenital heart defects,...
AGK Gene Sengers syndrome NGS Genetic Test
To diagnose Sengers syndrome by identifying mutations in the AGK gene using Next-Generation Sequenci...
EIF2AK4 Gene Pulmonary venoocclusive disease type 2 NGS Genetic Test
The purpose of this test is to identify mutations in the EIF2AK4 gene that cause Pulmonary Venoocclu...
KCNJ2 Gene Short QT syndrome type 3 NGS Genetic Test
To identify pathogenic mutations in the KCNJ2 gene associated with Short QT Syndrome Type 3, enablin...
CACNA1D Gene Sinoatrial node dysfunction and deafness NGS Genetic Test
The purpose of the CACNA1D Gene Test is to identify genetic mutations or variants in the CACNA1D gen...
MYH6 Gene Sick sinus syndrome type 3 NGS Genetic Test
To detect mutations in the MYH6 gene associated with sick sinus syndrome type 3, aiding in diagnosis...
SCN5A Gene Sudden infant death syndrome, susceptibility to NGS Genetic Test
To identify genetic mutations in the SCN5A gene that may increase susceptibility to sudden infant de...
ALDH1A2 Gene Tetralogy of Fallot NGS Genetic Test
To identify genetic mutations in the ALDH1A2 gene that may cause Tetralogy of Fallot, enabling early...
GATA4 Gene Tetralogy of Fallot NGS Genetic Test
The purpose of this test is to detect genetic mutations in the GATA4 gene that are linked to Tetralo...
ZFPM2 Gene Tetralogy of Fallot NGS Genetic Test
To detect mutations in the ZFPM2 gene associated with Tetralogy of Fallot, aiding in diagnosis, risk...
MED13L Gene Transposition of the great arteries, dextro-looped 1 NGS Genetic Test
The purpose of this test is to identify pathogenic variants in the MED13L gene that cause transposit...
SMAD2 Gene Thoracic aortic aneurysm dissection NGS Genetic Test
The purpose of this test is to identify mutations in the SMAD2 gene associated with thoracic aortic...
CITED2 Gene Ventricular septal defect type 2 NGS Genetic Test
To identify genetic mutations in the CITED2 gene associated with Ventricular Septal Defect type 2, a...
GATA4 Gene Ventricular septal defect type 1 NGS Genetic Test
To confirm a diagnosis of GATA4 gene-related ventricular septal defect type 1 through advanced genet...
RYR2 Gene Ventricular tachycardia, catecholaminergic polymorphic type 1 NGS Genetic Test
The purpose of the RYR2 Gene CPVT NGS Genetic Test is to identify pathogenic mutations in the RYR2 g...
CALM1 Gene Ventricular tachycardia, catecholaminergic polymorphic type 4 NGS Genetic Test
To detect mutations in the CALM1 gene that cause catecholaminergic polymorphic ventricular tachycard...
PRKAG2 Gene Wolff -Parkinson-White syndrome NGS Genetic Test
The purpose of this test is to detect mutations in the PRKAG2 gene associated with Wolff-Parkinson-W...
HTRA1 Gene CARASIL NGS Genetic Test
To identify mutations in the HTRA1 gene associated with CARASIL for diagnostic purposes and genetic...
RASA1 Gene Capillary malformation-arteriovenous malformation NGS Genetic Test
The purpose of this test is to detect mutations in the RASA1 gene that cause Capillary Malformation-...
PPARG Gene Carotid intimal medial thickness type 1 NGS Genetic Test
The purpose of this test is to identify genetic variations in the PPARG gene that are associated wit...
KRIT1 Gene Cerebral cavernous malformations type 1 NGS Genetic Test
The purpose of this test is to identify mutations in the KRIT1 gene to diagnose cerebral cavernous m...
CCM2 Gene Cerebral cavernous malformations type 2 NGS Genetic Test
To diagnose mutations in the CCM2 gene causing cerebral cavernous malformations type 2, enabling ear...
MCTP2 Gene Coarctation of the aorta NGS Genetic Test
To identify mutations in the MCTP2 gene that may cause coarctation of the aorta, facilitating early...
ITGA2 Gene Glycoprotein Ia C807T polymorphism NGS Genetic Test
The purpose of this test is to detect the ITGA2 C807T polymorphism to assess genetic risk for arteri...
JAM3 Gene Hemorrhagic destruction of the brain, subependymal calcification, and cataracts NGS Genetic Test
To detect genetic mutations in the JAM3 gene associated with hemorrhagic destruction of the brain, s...
NR3C2 Gene Hypertension early onset NGS Genetic Test
To identify mutations in the NR3C2 gene associated with early onset hypertension for accurate diagno...
CYP3A5 Gene Hypertension, salt-sensitive essential, susceptibility to NGS Genetic Test
To identify genetic susceptibility to salt-sensitive hypertension through CYP3A5 gene analysis, enab...
ADD2 Gene Hypertension, ADD2 related NGS Genetic Test
The purpose of this test is to identify genetic variations in the ADD2 gene that may be associated w...
NOS2 Gene Hypertension, susceptibility to NGS Genetic Test
To determine an individual's genetic susceptibility to hypertension by analyzing variations in the N...
TGFB2 Gene Loeys-Dietz syndrome type 4 NGS Genetic Test
The purpose of this test is to detect mutations in the TGFB2 gene associated with Loeys-Dietz Syndro...
GUCY1A3 Gene Moyamoya type 6 with achalasia NGS Genetic Test
To diagnose Moyamoya type 6 with Achalasia by identifying mutations in the GUCY1A3 gene using NGS te...
SERPINE1 Gene Plasminogen activator inhibitor type 1 NGS Genetic Test
To identify mutations or variations in the SERPINE1 gene that may increase the risk of vascular dise...
SLC6A2 Gene Orthostatic intolerance NGS Genetic Test
The purpose of the SLC6A2 Gene Orthostatic Intolerance NGS Genetic Test is to identify genetic varia...
RASA1 Gene Parkes Weber syndrome NGS Genetic Test
The purpose of this test is to confirm a diagnosis of Parkes Weber syndrome by detecting mutations i...
PROC Gene Protein C Deficiency, AD NGS Genetic Test
The purpose of the AD NGS Genetic Test is to identify mutations in the PROC gene that cause Protein...
ADA2 Gene Polyarteritis nodosa, childhood-onset NGS Genetic Test
To identify pathogenic mutations in the ADA2 gene that cause childhood-onset Polyarteritis Nodosa, a...
PROS1 Gene Protein S Deficiency, autosomal dominant NGS Genetic Test
To diagnose PROS1 gene mutations causing protein S deficiency, assess thrombosis risk, guide treatme...
CUL3 Gene Pseudohypoaldosteronism type 2E NGS Genetic Test
The purpose of the CUL3 Gene Pseudohypoaldosteronism type 2E NGS Genetic Test is to identify mutatio...
BMPR2 Gene Pulmonary hypertension, primary type NGS Genetic Test
To diagnose BMPR2 gene mutations causing hereditary pulmonary arterial hypertension, enabling early...
ADA2 Gene Sneddon syndrome NGS Genetic Test
The purpose of this test is to identify mutations in the ADA2 gene that cause Sneddon syndrome, aidi...
F2 Gene Thrombophilia due to thrombin defect NGS Genetic Test
The purpose of this test is to detect mutations in the F2 gene that cause thrombophilia, helping to...
GNA13 Gene Vascular system defects due to GNA13 deficiency NGS Genetic Test
The purpose of the GNA13 Gene NGS Genetic Test is to identify mutations in the GNA13 gene that cause...
ELN Gene Supravalvar aortic stenosis NGS Genetic Test
The purpose of this test is to identify mutations in the ELN gene that cause Supravalvar Aortic Sten...
CALCRL Gene Vascular system defects due to CALCRL deficiency NGS Genetic Test
The purpose of the CALCRL Gene NGS Genetic Test is to identify mutations or deficiencies in the CALC...
MT-TY Gene Focal segmental glomerulosclerosis and dilated cardiomyopath, MT-TY related NGS Genetic Test
The purpose of the MT-TY Gene NGS Genetic Test is to diagnose Focal Segmental Glomerulosclerosis and...
GATA4 Gene Atrial septal defect type 2 NGS Genetic Test
To detect mutations in the GATA4 gene associated with atrial septal defect type 2 (ASD2) for diagnos...