Molecular Diagnostics tests in Dubai & UAE

Compare available Molecular Diagnostics tests, their listed prices and the information provided for each option. Test selection and preparation should be discussed with your clinician.

Tests in this category

781

Listed price range

550.00–150,000.00 AED

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Molecular Diagnostics test prices

Showing 736–750 of 781 matching tests.

Molecular Diagnostics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-1080 Thiopurine Methyltransferase (TPMT Test This test evaluates genetic variants in the TPMT gene that affect the activity of the Thiopurine Methyltransferase enzyme, predicting drug metabolism capacity.	Peripheral whole blood (EDTA or citrate)	5–7 business days	800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TPMT gene variant alleles (2, 3A, 3B, 3C)", "Predicted thiopurine drug metabolism capacity"] Parameters [] Preparation ["No fasting or special preparation required.", "Provide valid Emirates ID and prescription."] Indications ["Prior to initiating thiopurine therapy (azathioprine, 6-mercaptopurine, thioguanine)", "Patients with unexplained severe myelosuppression while on thiopurines"] Measurement technique Confirm with laboratory Codes LOINC: 90330-2 ICD-10: Z13.5 Clinical summary This test evaluates genetic variants in the TPMT gene that affect the activity of the Thiopurine Methyltransferase enzyme, predicting drug metabolism capacity.
TEST-3456 THRB Gene Thyroid Hormone Resistance Genetic Test This genetic test screens for germline mutations in the THRB gene associated with Resistance to Thyroid Hormone (RTH). It identifies pathogenic variants causing reduced tissue resp...	Whole Blood (EDTA), FTA Card, or Extracted DNA	3–4 Weeks (21–28 Business Days)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the THRB gene", "Germline mutations causing RTH"] Parameters [] Preparation ["No fasting required", "No specific medication or diet restrictions"] Indications ["Diagnosis of Resistance to Thyroid Hormone (RTH)", "Evaluation of patients with unexplained abnormal thyroid function tests", "Genetic counselling for families with RTH"] Measurement technique Confirm with laboratory Codes LOINC: 21670-1 ICD-10: E07.8 Clinical summary This genetic test screens for germline mutations in the THRB gene associated with Resistance to Thyroid Hormone (RTH). It identifies pathogenic variants causing reduced tissue responsiveness to thyroid hormones.
TEST-433 Thyroid Cancer Prognostication NGS Panel Test This test evaluates somatic mutations, gene fusions, and expression patterns in thyroid cancer tissue or aspirate samples.	Tissue or Fine Needle Aspirate	4 weeks (28 days)	5,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Somatic mutations (e.g., BRAF, RAS, RET, TERT)", "Gene fusions (e.g., RET/PTC, PAX8/PPARγ)", "Expression patterns"] Parameters [] Preparation ["No specific patient preparation required", "Do not discontinue prescribed medication without consulting your doctor"] Indications ["Diagnosis of thyroid cancer", "Prognostication of thyroid cancer", "Guidance for targeted therapy selection"] Measurement technique Confirm with laboratory Codes LOINC: 98542-0 ICD-10: C73 Clinical summary This test evaluates somatic mutations, gene fusions, and expression patterns in thyroid cancer tissue or aspirate samples.
TEST-4403 TLL1 Gene Atrial Septal Defect Type 6 Genetic Test This test identifies pathogenic variants in the TLL1 gene associated with atrial septal defect type 6 (ASD6).	Peripheral blood (whole blood, EDTA tube)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the TLL1 gene", "Single nucleotide variants", "Small insertions/deletions"] Parameters [] Preparation ["No fasting required"] Indications ["Clinical suspicion of atrial septal defect type 6 (ASD6)", "Congenital heart malformation"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: Q21.1 Clinical summary This test identifies pathogenic variants in the TLL1 gene associated with atrial septal defect type 6 (ASD6).
TEST-5047 TLR3 Gene Herpes Simplex Encephalitis Type 2 Susceptibility Test This diagnostic test evaluates the TLR3 gene for pathogenic variants associated with increased susceptibility to herpes simplex encephalitis type 2.	Peripheral whole blood (3–5 mL EDTA) or extracted genomic DNA (2 µg minimum)	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the TLR3 gene", "Loss-of-function mutations"] Parameters [] Preparation ["No fasting required", "Inform phlebotomist of all medications, especially antivirals or immunosuppressants"] Indications ["Individuals with a personal or family history suggestive of increased susceptibility to HSV-2 encephalitis", "Proactive risk assessment in specific populations"] Measurement technique Confirm with laboratory Codes LOINC: 48767-8 ICD-10: Z15.89, Z86.19 Clinical summary This diagnostic test evaluates the TLR3 gene for pathogenic variants associated with increased susceptibility to herpes simplex encephalitis type 2.
TEST-2649 TLR5 Gene Legionnaire Disease Susceptibility Genetic Test This genetic test evaluates variants in the TLR5 gene associated with susceptibility to Legionnaires' disease.	Whole Blood, Extracted DNA, or FTA Card Sample	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TLR5 gene variants", "Immune recognition of Legionella pneumophila"] Parameters [] Preparation ["No fasting required", "Genetic counselling session arranged beforehand"] Indications ["Proactive pulmonary risk assessment", "Proactive cardiovascular risk assessment", "Individuals with family history of Legionnaires' disease"] Measurement technique Confirm with laboratory Codes LOINC: 82325-7 ICD-10: Z15.09 Clinical summary This genetic test evaluates variants in the TLR5 gene associated with susceptibility to Legionnaires' disease.
TEST-1929 TMEM127 Gene Pheochromocytoma Type 8 Genetic Test This genetic test detects mutations in the TMEM127 gene associated with hereditary pheochromocytoma type 8.	Peripheral whole blood (EDTA), extracted DNA, or FTA card	3–4 weeks from sample receipt	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Germline mutations in the TMEM127 gene", "Coding exons and splice sites of TMEM127"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medications without consulting your physician"] Indications ["Individuals with a personal or family history of pheochromocytoma", "Risk assessment for hereditary pheochromocytoma", "Cascade testing for family members"] Measurement technique Confirm with laboratory Codes LOINC: 74883-4 ICD-10: Z15.09, D44.7 Clinical summary This genetic test detects mutations in the TMEM127 gene associated with hereditary pheochromocytoma type 8.
TEST-3256 TMPRSS6 Gene Analysis for Iron-Refractory Iron Deficiency Anemia (IRIDA) via NGS Test This test identifies pathogenic variants in the TMPRSS6 gene associated with Iron-Refractory Iron Deficiency Anemia (IRIDA).	Peripheral Whole Blood (2–3 mL) or Dried Blood Spot	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the TMPRSS6 gene", "Zygosity of variants"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medications unless instructed by physician"] Indications ["Suspected IRIDA", "Family history of IRIDA", "Need for definitive diagnosis to guide treatment"] Measurement technique Confirm with laboratory Codes LOINC: 51924-9 ICD-10: D50.8 Clinical summary This test identifies pathogenic variants in the TMPRSS6 gene associated with Iron-Refractory Iron Deficiency Anemia (IRIDA).
TEST-570 Toxoplasma gondii DNA Quantitative PCR (Bacterial Load) Test This test directly measures the amount of Toxoplasma gondii DNA in a sample to assess active parasitic infection.	Whole blood, serum, urine, or aqueous humor	36 hours (telephone) / 48 hours (secure email)	800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Toxoplasma gondii DNA", "Parasitic Load"] Parameters [{"name": "Limit of Detection (LOD)", "reference_range": "5 DNA copies per mL"}] Preparation ["No fasting required", "Sign informed consent form", "Provide brief clinical history summary"] Indications ["Diagnosis of acute toxoplasmosis", "Monitoring response to anti-parasitic therapy", "Assessment of congenital transmission risk during pregnancy", "Differentiation between active and latent infection"] Measurement technique Confirm with laboratory Codes LOINC: 24111-8 ICD-10: B58.9, B58.0, B58.8 Clinical summary This test directly measures the amount of Toxoplasma gondii DNA in a sample to assess active parasitic infection.
TEST-5843 TPMT Genotyping (NGS) for Thiopurine Methyltransferase Deficiency Test This test identifies genetic variations in the TPMT gene that affect the metabolism of thiopurine drugs, guiding safe dosing.	Whole blood (EDTA), extracted DNA, or dried blood spot on FTA card	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TPMT gene variants", "TPMT enzyme activity phenotype"] Parameters [] Preparation [] Indications ["Patients requiring thiopurine medications (azathioprine, 6-mercaptopurine, thioguanine)", "Organ transplantation", "Inflammatory bowel disease", "Autoimmune hepatitis", "Rheumatologic conditions", "Childhood acute lymphoblastic leukemia"] Measurement technique Confirm with laboratory Codes LOINC: 92806-3 ICD-10: Z13.89 Clinical summary This test identifies genetic variations in the TPMT gene that affect the metabolism of thiopurine drugs, guiding safe dosing.
TEST-3507 TPO Gene Thyroid Dyshormonogenesis Type 2A Genetic Test This genetic test identifies pathogenic variants in the TPO gene associated with thyroid dyshormonogenesis type 2A, a cause of congenital hypothyroidism.	Whole Blood, Dried Blood Spot (FTA Card), or Extracted Genomic DNA	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the TPO gene"] Parameters [] Preparation [] Indications ["Infants with congenital hypothyroidism of unknown etiology", "Children with persistent goiter and elevated TSH", "Adults with a family history of dyshormonogenetic goiter", "Carrier testing for at-risk relatives"] Measurement technique Confirm with laboratory Codes LOINC: 81260-1 ICD-10: E03.1, E07.1 Clinical summary This genetic test identifies pathogenic variants in the TPO gene associated with thyroid dyshormonogenesis type 2A, a cause of congenital hypothyroidism.
TEST-4824 TRIM32 Gene Limb‑Girdle Muscular Dystrophy Autosomal Recessive Type 2H Genetic Test This genetic test screens the TRIM32 gene for pathogenic variants associated with autosomal recessive limb-girdle muscular dystrophy type 2H (LGMD2H).	Peripheral whole blood (3–5 mL in EDTA tube), extracted DNA, or dried blood spot (FTA card).	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the TRIM32 gene", "Coding region and splice sites of TRIM32"] Parameters [] Preparation ["No fasting required", "No medication changes required", "Pre-genetic counselling session mandatory"] Indications ["Suspected diagnosis of Limb-Girdle Muscular Dystrophy Type 2H", "Family history of LGMD2H", "Genetic counselling for at-risk relatives"] Measurement technique Confirm with laboratory Codes LOINC: 49733-2 ICD-10: G71.03, G71.0 Clinical summary This genetic test screens the TRIM32 gene for pathogenic variants associated with autosomal recessive limb-girdle muscular dystrophy type 2H (LGMD2H).
TEST-2519 TRIM37 Gene Mulibrey Nanism Genetic Test This test detects pathogenic variants in the TRIM37 gene associated with Mulibrey nanism.	Whole blood (EDTA), Extracted DNA, or FTA Card	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the TRIM37 gene", "Single-nucleotide variants", "Small insertions/deletions", "Copy-number alterations (via NGS and MLPA reflex)"] Parameters [] Preparation ["No specific fasting required", "No medication or diet restrictions"] Indications ["Suspected diagnosis of Mulibrey nanism based on clinical features", "Family history of Mulibrey nanism", "Carrier screening in relatives of affected individuals"] Measurement technique Confirm with laboratory Codes LOINC: 8100-9 ICD-10: Q87.8 Clinical summary This test detects pathogenic variants in the TRIM37 gene associated with Mulibrey nanism.
TEST-3172 TRNT1 Gene Sideroblastic Anemia with B-Cell Immunodeficiency, Periodic Fevers, and Developmental Delay Genetic Test This genetic test analyzes the TRNT1 gene to detect mutations causing a rare syndrome involving anemia, immune deficiency, fevers, and developmental delay.	Whole Blood, Extracted DNA, FTA Card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the TRNT1 gene", "Copy Number Variations (CNVs) in the TRNT1 gene"] Parameters [] Preparation ["No special preparation required", "Genetic counselling session is mandatory before the test"] Indications ["Suspected TRNT1-related disease based on clinical presentation", "Family history of TRNT1-related disease"] Measurement technique Confirm with laboratory Codes LOINC: 92891-0 ICD-10: D64.0, D81.4, R50.9, F80.9 Clinical summary This genetic test analyzes the TRNT1 gene to detect mutations causing a rare syndrome involving anemia, immune deficiency, fevers, and developmental delay.
TEST-4129 TRPM4 Gene Progressive Familial Heart Block Genetic Test This test evaluates the TRPM4 gene for pathogenic variants associated with progressive familial heart block type IA (PFHB1). It utilizes next-generation sequencing (NGS) to detect...	Whole Blood (EDTA) or Saliva (Oragene DNA Saliva Kit)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the TRPM4 gene", "Single-nucleotide variants", "Insertions/deletions", "Splice-site alterations"] Parameters [] Preparation ["No specific fasting required.", "Inform the lab of any current medications."] Indications ["Individuals with a clinical suspicion of progressive familial heart block type IA (PFHB1)", "Family members of individuals diagnosed with a pathogenic TRPM4 variant", "Cascade family screening for inherited arrhythmia risk"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: I44.2 Clinical summary This test evaluates the TRPM4 gene for pathogenic variants associated with progressive familial heart block type IA (PFHB1). It utilizes next-generation sequencing (NGS) to detect genetic mutations.

Category overview

Molecular Diagnostics: overview

When complex health questions arise, evaluating your health at the cellular level provides the definitive clarity necessary for proactive care. At DNA Labs UAE, our Molecular Diagnostics services harness the power of advanced nucleic acid amplification and real-time PCR technologies to detect diseases with unparalleled sensitivity. From identifying viral loads to pinpointing genetic markers, our specialized molecular testing in the UAE gives your healthcare provider the precise data needed to customize your medical strategy. Trust in one of the leading diagnostic labs in Dubai and the UAE to process your samples with rigorous confidentiality and exceptionally fast, accurate turnaround times. Step forward with absolute confidence. View our molecular diagnostics profiles below, request a seamless home sample collection, or contact our specialized team to book your test.

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Molecular Diagnostics tests in Dubai & UAE

Molecular Diagnostics test prices

Molecular Diagnostics: overview

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