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Diagnostic options Β· UAE

Biochemistry tests in Dubai & UAE

Compare available Biochemistry 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

1,113

Listed price range

450.00–30,000.00 AED

Clinical preparation

Confirm test-specific instructions with your clinician or laboratory.

Compare available tests

Biochemistry test prices

Showing 1006–1020 of 1,113 matching tests.

Biochemistry diagnostic tests, details, and listed prices
Test and description Specimen Typical duration Price Options
TEST-3467
TG Gene Thyroid Dyshormonogenesis Type 3 Genetic Test

This genetic test detects pathogenic variants in the thyroglobulin (TG) gene associated with congenital hypothyroidism and goitre.

Whole Blood (Peripheral) 21 calendar days 2,800.00 AED
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What it measures
["Pathogenic variants in the TG gene", "Full coding region and splice sites of the TG gene"]
Parameters
[]
Preparation
["No specific patient preparation required"]
Indications
["Suspected thyroid dyshormonogenesis", "Congenital hypothyroidism with goitre", "Family history of thyroid disorders"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 98137-4 ICD-10: E07.1, Z13.29, Z14.8
Clinical summary
This genetic test detects pathogenic variants in the thyroglobulin (TG) gene associated with congenital hypothyroidism and goitre.
TEST-3026
TGFB1 Gene Camurati‑Engelmann Disease Genetic Test

This test evaluates the entire coding region and splice sites of the TGFB1 gene for variants associated with Camurati-Engelmann disease.

Whole blood (EDTA), extracted genomic DNA, or FTA card spot 3 to 4 weeks 2,800.00 AED
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What it measures
["TGFB1 gene variants", "Single nucleotide variants (SNVs)", "Insertions/Deletions (Indels)"]
Parameters
[]
Preparation
["Pre-test genetic counselling required", "Written informed consent required", "Three-generation pedigree chart required"]
Indications
["Suspected Camurati-Engelmann disease", "Progressive diaphyseal dysplasia", "Family history of bone dysplasias"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 82939-0 ICD-10: Q78.3
Clinical summary
This test evaluates the entire coding region and splice sites of the TGFB1 gene for variants associated with Camurati-Engelmann disease.
TEST-4823
TGFBR1 Gene Loeys-Dietz Syndrome Type 1A Genetic Test

This test detects pathogenic variants in the TGFBR1 gene associated with Loeys-Dietz syndrome type 1A.

EDTA whole blood, Extracted DNA, or FTA Card 3–4 Weeks 2,800.00 AED
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What it measures
["Pathogenic variants in the TGFBR1 gene", "Copy Number Variants (CNVs) in TGFBR1"]
Parameters
[]
Preparation
["No specific fasting required", "Continue prescribed medications unless advised otherwise by a physician"]
Indications
["Suspected diagnosis of Loeys-Dietz syndrome type 1A", "Family history of Loeys-Dietz syndrome", "Genetic counseling for at-risk individuals"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 81307-4 ICD-10: Q87.89
Clinical summary
This test detects pathogenic variants in the TGFBR1 gene associated with Loeys-Dietz syndrome type 1A.
TEST-2751
TGIF1 Gene Holoprosencephaly Type 4 Genetic Test

This genetic test analyzes the TGIF1 gene to detect pathogenic variants associated with holoprosencephaly type 4.

Whole Blood (EDTA), Extracted DNA, or FTA Card 3–4 weeks 2,800.00 AED
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View test specifications and preparation
What it measures
["Pathogenic variants in the TGIF1 gene", "Coding regions and splice sites of the TGIF1 gene"]
Parameters
[]
Preparation
["No special preparation is needed", "Do not discontinue prescribed medications"]
Indications
["Suspected holoprosencephaly type 4", "Family history of holoprosencephaly", "Need for precise prognosis and recurrence risk assessment"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 55233-1 ICD-10: Q04.2
Clinical summary
This genetic test analyzes the TGIF1 gene to detect pathogenic variants associated with holoprosencephaly type 4.
TEST-5677
TH Gene Segawa Syndrome, Autosomal Recessive Genetic Test

This test evaluates the tyrosine hydroxylase (TH) gene for pathogenic variants associated with autosomal recessive Segawa syndrome (dopa-responsive dystonia). It utilizes Next-Gene...

Whole blood (EDTA), pre-extracted DNA, or FTA card 3–4 weeks 2,800.00 AED
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View test specifications and preparation
What it measures
["Pathogenic variants in the TH gene", "Single nucleotide variants (SNVs)", "Insertions/deletions (indels)", "Copy number variations (CNVs)"]
Parameters
[]
Preparation
["No specific fasting required", "Inform lab of any current medications"]
Indications
["Suspected Segawa syndrome (dopa-responsive dystonia)", "Early-onset dystonia of unknown cause", "Family history of Segawa syndrome"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 81309-1 ICD-10: G24.1
Clinical summary
This test evaluates the tyrosine hydroxylase (TH) gene for pathogenic variants associated with autosomal recessive Segawa syndrome (dopa-responsive dystonia). It utilizes Next-Generation Sequencing (NGS) for comprehensive analysis.
TEST-3265
Thalassemia Beta Complete Gene Analysis with Maternal Cell Contamination (MCC) Test

This test evaluates the fetal beta-globin gene for mutations associated with beta-thalassemia and confirms the absence of maternal cell contamination.

Amniotic fluid or Chorionic Villus Sample 21 Working Days 2,800.00 AED
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What it measures
["Fetal beta-globin gene pathogenic variants", "Maternal Cell Contamination (MCC)"]
Parameters
[]
Preparation
["Discuss complete medical history with the referring specialist.", "Do not discontinue prescribed medication without explicit instruction from the supervising physician."]
Indications
["Prenatal screening for beta-thalassemia", "Risk assessment based on parental carrier status", "Ultrasound findings suggestive of fetal anemia"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 21620-0 ICD-10: D56.1
Clinical summary
This test evaluates the fetal beta-globin gene for mutations associated with beta-thalassemia and confirms the absence of maternal cell contamination.
TEST-3259
Thalassemia Beta Mutation Analysis Test

This test identifies pathogenic variants in the HBB gene associated with beta-thalassemia.

Peripheral Whole Blood (Lavender Top EDTA) 5 working days 1,200.00 AED
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What it measures
["Pathogenic variants in the HBB gene"]
Parameters
[]
Preparation
[]
Indications
["Diagnostic confirmation of beta-thalassemia", "Carrier screening", "Informed reproductive planning"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 46738-3 ICD-10: D56.1, D56.9, Z31.430
Clinical summary
This test identifies pathogenic variants in the HBB gene associated with beta-thalassemia.
TEST-3273
Thallium 24-Hour Urine Test

This test measures the amount of thallium excreted in urine over a 24-hour period to assess exposure levels.

24-Hour Urine Collection Next-day (sample received by 6 PM) 850.00 AED
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What it measures
["Thallium excretion", "Renal clearance of thallium"]
Parameters
[{"name": "Thallium", "reference_range": "0.05 Β΅g/L (Adjusted for local UAE population)"}]
Preparation
["Avoid gadolinium or iodine contrast media for 96 hours prior", "Use provided metal-free container", "Wear powder-free gloves", "Record total urine volume", "Refrigerate sample at 2–8Β°C", "Do not freeze the specimen"]
Indications
["Suspected chronic industrial exposure", "Occupational health surveillance", "Toxicology follow-up", "Monitoring chelation therapy effectiveness"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 2891-3 ICD-10: Z77.098
Clinical summary
This test measures the amount of thallium excreted in urine over a 24-hour period to assess exposure levels.
TEST-3266
Thallium Blood Test

This diagnostic test evaluates the concentration of thallium in whole blood to detect toxic exposure.

Whole Blood Next-day report (if collected by 6 PM) 750.00 AED
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What it measures
["Total Thallium"]
Parameters
[{"name": "Thallium", "reference_range": null}]
Preparation
["Avoid Gadolinium- or Iodine-containing contrast media for at least 96 hours prior to collection"]
Indications
["Suspected thallium poisoning", "Exposure to thallium-containing substances", "Unexplained neurological symptoms after potential exposure"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 69263-8 ICD-10: T60.4X
Clinical summary
This diagnostic test evaluates the concentration of thallium in whole blood to detect toxic exposure.
TEST-3277
Thallium Random Urine Test

This diagnostic test evaluates recent exposure to thallium, a toxic heavy metal, by measuring its concentration in a random urine sample.

Urine (random) Next day (if sample received by 6 PM) 750.00 AED
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View test specifications and preparation
What it measures
["Thallium concentration in urine"]
Parameters
[{"name": "Thallium", "reference_range": "0.1 Β΅g/L (Detection Limit)"}]
Preparation
["No fasting required", "Avoid Gadolinium or Iodine-based contrast media for at least 96 hours prior to collection"]
Indications
["Suspected thallium poisoning", "Occupational exposure monitoring", "Environmental exposure monitoring", "Diagnosis of industrial toxicity", "Investigation of unexplained neuropathy"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 27029-4 ICD-10: Z77.0
Clinical summary
This diagnostic test evaluates recent exposure to thallium, a toxic heavy metal, by measuring its concentration in a random urine sample.
TEST-3272
Thioridazine Test

This diagnostic test evaluates the concentration of thioridazine in the patient's serum.

Blood (Serum) 14–21 days 1,900.00 AED
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What it measures
["Serum thioridazine concentration"]
Parameters
[{"name": "Serum Thioridazine", "reference_range": null}]
Preparation
["No fasting required", "Schedule blood draw just before next dose for trough level", "Complete mandatory consent form (Form 35)", "Note all current medications"]
Indications
["Monitoring patients on long-term thioridazine therapy", "Suspected non-adherence to medication", "Potential drug interactions affecting thioridazine metabolism", "Patients with CYP2D6 polymorphisms", "Assessing therapeutic range"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 3948-1 ICD-10: Z51.81
Clinical summary
This diagnostic test evaluates the concentration of thioridazine in the patient's serum.
TEST-4532
THSD1 Gene Thrombospondin Type 1 Domain-Containing Protein 1 Genetic Test

This test evaluates the entire coding region and splice sites of the THSD1 gene for pathogenic variants.

Peripheral Blood, FTA Card, or Extracted DNA 3 to 4 Weeks 2,800.00 AED
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View test specifications and preparation
What it measures
["Pathogenic variants in THSD1 gene coding regions", "Pathogenic variants in THSD1 gene splice sites"]
Parameters
[]
Preparation
["No fasting required", "No specific medication or diet restrictions"]
Indications
["Suspected hereditary disorders affecting bone", "Suspected hereditary disorders affecting skin", "Suspected hereditary disorders affecting the immune system"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 88850-6 ICD-10: Z13.71
Clinical summary
This test evaluates the entire coding region and splice sites of the THSD1 gene for pathogenic variants.
TEST-3293
Thyroid Comprehensive Panel Test

This diagnostic test evaluates thyroid hormone levels (TSH, Free T4, Free T3) and thyroid autoimmunity (anti-TPO/anti-thyroglobulin antibodies). It helps diagnose and differentiate...

Peripheral venous blood (serum) Same day (if collected before 10 AM) / 24 hours maximum 800.00 AED
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View test specifications and preparation
What it measures
["TSH (Thyroid Stimulating Hormone)", "Free T4 (Free Thyroxine)", "Free T3 (Free Triiodothyronine)", "Anti-TPO Antibodies (Thyroid Peroxidase Antibodies)", "Anti-Thyroglobulin Antibodies"]
Parameters
[{"name": "TSH", "reference_range": null}, {"name": "Free T4", "reference_range": null}, {"name": "Free T3", "reference_range": null}, {"name": "Anti-TPO Antibodies", "reference_range": null}, {"name": "Anti-Thyroglobulin Antibodies", "reference_range": null}]
Preparation
["No fasting required", "Avoid heavy fatty meals 2 hours prior to collection", "Inform phlebotomist if pregnant", "Guardian presence required for minors"]
Indications
["Screening for thyroid dysfunction", "Diagnosis of hypothyroidism or hyperthyroidism", "Evaluation of autoimmune thyroid disease (Hashimoto's, Graves')", "Monitoring thyroid treatment"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 54224-6 ICD-10: E07.9
Clinical summary
This diagnostic test evaluates thyroid hormone levels (TSH, Free T4, Free T3) and thyroid autoimmunity (anti-TPO/anti-thyroglobulin antibodies). It helps diagnose and differentiate various thyroid conditions.
TEST-4185
TIMM8A Gene Dystonia-Deafness Syndrome Genetic Test

This genetic test analyzes the TIMM8A gene to detect mutations associated with Mohr‑Tranebjaerg syndrome, a rare X-linked disorder causing dystonia and deafness.

Peripheral Whole Blood 3 – 4 Weeks 2,800.00 AED
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View test specifications and preparation
What it measures
["Pathogenic variants in the TIMM8A gene", "Coding region sequence of the TIMM8A gene"]
Parameters
[{"name": "Analytical Sensitivity", "reference_range": ">99.9%"}, {"name": "Methodology", "reference_range": "Next-Generation Sequencing (NGS), full gene"}, {"name": "Clinical Reporting", "reference_range": "DHA‑compliant, detailed ACMG classification"}]
Preparation
["No specific fasting required", "Inform lab of current medications"]
Indications
["Suspected Mohr‑Tranebjaerg syndrome", "Family history of dystonia and deafness", "Genetic counseling for at-risk individuals"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 93175-2 ICD-10: G24.1, H90.5
Clinical summary
This genetic test analyzes the TIMM8A gene to detect mutations associated with Mohr‑Tranebjaerg syndrome, a rare X-linked disorder causing dystonia and deafness.
TEST-4394
TIMP1 Gene Bicuspid Aortic Valve Genetic Test

This test evaluates for pathogenic variants in the TIMP1 gene associated with an increased risk of developing bicuspid aortic valve.

Whole blood (EDTA), FTA card, or extracted genomic DNA 3 to 4 weeks 2,800.00 AED
View
View test specifications and preparation
What it measures
["Pathogenic variants in the TIMP1 gene"]
Parameters
[]
Preparation
[]
Indications
["Family history of bicuspid aortic valve", "Personal history suggestive of BAV", "Proactive cardiovascular risk assessment"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 81247-9 ICD-10: Q23.1, Z13.79
Clinical summary
This test evaluates for pathogenic variants in the TIMP1 gene associated with an increased risk of developing bicuspid aortic valve.

Category overview

Biochemistry: overview

Seeking clarity about your body's essential functions is vital for long-term well-being. At DNA Labs UAE, our Biochemistry services utilize advanced automated analyzers to evaluate enzymes, proteins, and metabolites in your blood. Whether you need routine metabolic panels or specialized biochemical testing in the UAE, these tests provide critical data to guide your physician's medical plan. As a leading diagnostic lab in Dubai and the UAE, we guarantee strict confidentiality and rapid, accurate turnaround times. Take charge of your health today. Explore our biochemistry diagnostics below, schedule a convenient home sample collection, or contact our specialists to book your test.

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Use the test details as a conversation starter

The right diagnostic option depends on your reason for testing and individual circumstances. Check the listed specimen and timing, then confirm any preparation requirements with the ordering clinician or laboratory before collection.

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