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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 1081–1095 of 1,113 matching tests.

Biochemistry diagnostic tests, details, and listed prices
Test and description Specimen Typical duration Price Options
TEST-3387
Vitamin B2 (Riboflavin) Test

This diagnostic test evaluates the concentration of riboflavin (Vitamin B2) in blood plasma.

Plasma (EDTA) 2–3 weeks from sample receipt (batch testing) 1,800.00 AED
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What it measures
["Riboflavin levels in plasma", "Energy metabolism indicators"]
Parameters
[{"name": "Riboflavin", "reference_range": null}]
Preparation
["Overnight fasting (10–12 hours) is mandatory. Only plain water is allowed.", "Avoid any vitamin supplements, especially B-complex, for at least 24 hours before collection."]
Indications
["First-line screening for unexplained fatigue", "Suspected malnutrition", "Dietary assessment", "Vegan/vegetarian planning", "Eating disorder management", "Micronutrient optimization", "Root-cause analysis of energy metabolism"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 2939-3 ICD-10: E53.0, Z13.2
Clinical summary
This diagnostic test evaluates the concentration of riboflavin (Vitamin B2) in blood plasma.
TEST-3401
Vitamin B6 (Pyridoxine) Test

This test measures the active form of Vitamin B6 (pyridoxal 5β€²-phosphate) in plasma to assess nutritional status and diagnose deficiency.

Plasma (EDTA) 2–3 weeks (batch processing; sample must be received by the 7th of the month) 1,200.00 AED
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What it measures
["Plasma Pyridoxal 5β€²-phosphate (PLP)", "Vitamin B6 activity"]
Parameters
[{"name": "Pyridoxal 5β€²-phosphate (PLP)", "reference_range": "Age- and sex-adjusted reference ranges provided in report"}]
Preparation
["Overnight fasting (10–12 hours) mandatory", "Avoid high-dose pyridoxine supplements 48 hours prior", "Inform physician of all medications and supplements"]
Indications
["Suspected Vitamin B6 deficiency", "Evaluation of unexplained peripheral neuropathy", "Nutritional assessment in malabsorption syndromes", "Monitoring Vitamin B6 supplementation", "Investigation of microcytic or sideroblastic anemias"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 2131-5 ICD-10: E53.1
Clinical summary
This test measures the active form of Vitamin B6 (pyridoxal 5β€²-phosphate) in plasma to assess nutritional status and diagnose deficiency.
TEST-3391
Vitamin C (Ascorbic Acid) Test

This diagnostic test evaluates the circulating level of ascorbic acid (Vitamin C) in serum to assess nutritional status.

Serum 2–3 weeks from sample receipt 2,000.00 AED
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What it measures
["Serum Ascorbic Acid (Vitamin C) level"]
Parameters
[{"name": "Ascorbic Acid (Vitamin C)", "reference_range": null}]
Preparation
["Fast overnight (10–12 hours)", "Avoid all vitamin supplements, fresh fruits, and vitamin-enriched drinks for at least 24 hours before collection"]
Indications
["Suspected clinical deficiency (Scurvy)", "Monitoring supplementation efficacy", "Evaluating oxidative stress-related malnutrition", "Patients with malabsorption", "Patients with chronic illness"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 41695-0 ICD-10: E54
Clinical summary
This diagnostic test evaluates the circulating level of ascorbic acid (Vitamin C) in serum to assess nutritional status.
TEST-3406
Vitamin D 1,25-Dihydroxy Test (Calcitriol)

This diagnostic test evaluates the level of the active form of Vitamin D (Calcitriol) in the blood.

Serum or plasma Same day if sample received by 11 AM; otherwise next working day 850.00 AED
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What it measures
["1,25-Dihydroxyvitamin D (Calcitriol)", "Calcium metabolism regulation"]
Parameters
[{"name": "1,25-Dihydroxyvitamin D (Calcitriol)", "reference_range": null}]
Preparation
["No special preparation required", "Patient can eat, drink, and take medications as usual"]
Indications
["Evaluation of calcium metabolism disorders", "Diagnosis of parathyroid disorders", "Diagnosis of renal disorders", "Investigation of granulomatous diseases", "Monitoring response to vitamin D therapy"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 14854-0 ICD-10: E55.9, E20.9
Clinical summary
This diagnostic test evaluates the level of the active form of Vitamin D (Calcitriol) in the blood.
TEST-3410
Vitamin D Comprehensive Test

This diagnostic test evaluates the levels of 25-hydroxyvitamin D (D2 and D3) in the blood serum.

Blood (serum) Same-day (daily processing) 550.00 AED
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What it measures
["25-hydroxyvitamin D (D2)", "25-hydroxyvitamin D (D3)"]
Parameters
[{"name": "25-Hydroxyvitamin D (D2)", "reference_range": null}, {"name": "25-Hydroxyvitamin D (D3)", "reference_range": null}]
Preparation
["No fasting required", "No specific dietary restrictions"]
Indications
["Suspected vitamin D deficiency", "Monitoring vitamin D therapy", "Assessment of bone health", "Evaluation of metabolic disorders"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 14682-9 ICD-10: E55.9
Clinical summary
This diagnostic test evaluates the levels of 25-hydroxyvitamin D (D2 and D3) in the blood serum.
TEST-3399
Vitamin D Screening Test

This test measures the level of 25-hydroxyvitamin D in the blood to assess vitamin D status.

Serum or Plasma (Peripheral Whole Blood) Same-day (daily batch processing) 550.00 AED
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What it measures
["25-hydroxyvitamin D (Calcidiol)", "Bone metabolism indicator", "Immune function indicator"]
Parameters
[{"name": "25-Hydroxyvitamin D", "reference_range": "Severe deficiency (100 ng/mL)"}]
Preparation
["No fasting required", "Inform phlebotomist of regular medications"]
Indications
["Screening for vitamin D deficiency or insufficiency", "Monitoring vitamin D supplementation therapy", "Evaluating risk of osteomalacia or osteoporosis", "Assessing immune function"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 35365-6 ICD-10: E55.9
Clinical summary
This test measures the level of 25-hydroxyvitamin D in the blood to assess vitamin D status.
TEST-3414
Vitamin D Ultrasensitive Test

This diagnostic test evaluates the level of 25-hydroxyvitamin D in the blood, providing a precise measure of the body's vitamin D status.

Blood (Serum or Plasma) Same Day (sample by 11 am) 550.00 AED
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What it measures
["25-hydroxyvitamin D (Calcidiol)", "Vitamin D Status"]
Parameters
[{"name": "25-Hydroxyvitamin D", "reference_range": "null"}]
Preparation
["No fasting required", "Maintain usual diet and hydration"]
Indications
["Suspected vitamin D deficiency or insufficiency", "Monitoring vitamin D therapy", "Evaluation of bone metabolism disorders (e.g., osteoporosis)", "Assessment of immune function", "Screening in high-risk populations"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 62292-9 ICD-10: E55.9
Clinical summary
This diagnostic test evaluates the level of 25-hydroxyvitamin D in the blood, providing a precise measure of the body's vitamin D status.
TEST-3404
Vitamin E (Tocopherol) Test

This diagnostic test evaluates serum alpha-tocopherol levels to assess vitamin E status and fat-soluble vitamin absorption.

Serum 3 business days 850.00 AED
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What it measures
["Serum alpha-tocopherol", "Antioxidant status", "Fat-soluble vitamin absorption"]
Parameters
[{"name": "Alpha-Tocopherol", "reference_range": null}]
Preparation
["Overnight fasting for 10–12 hours", "Avoid high-dose vitamin E, A, or K supplements before the test", "Inform team of all medications, especially anticoagulants"]
Indications
["Suspected vitamin E deficiency", "Malabsorption syndromes", "Monitoring excessive supplementation", "Genetic transport disorders"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 11130-7 ICD-10: E56.0, E56.1
Clinical summary
This diagnostic test evaluates serum alpha-tocopherol levels to assess vitamin E status and fat-soluble vitamin absorption.
TEST-3407
Vitamin Profile Extended (Comprehensive Nutritional Assessment) Test

This diagnostic test quantitatively evaluates levels of essential fat-soluble and water-soluble vitamins in serum.

Serum Sample collected by Friday 9 AM β†’ report delivered Tuesday afternoon 1,800.00 AED
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What it measures
["Fat-soluble vitamins (A, D, E, K)", "Water-soluble vitamins (B-complex, Folate)", "Vitamin C"]
Parameters
[{"name": "Vitamin A", "reference_range": null}, {"name": "Vitamin B1 (Thiamine)", "reference_range": null}, {"name": "Vitamin B2 (Riboflavin)", "reference_range": null}, {"name": "Vitamin B6 (Pyridoxine)", "reference_range": null}, {"name": "Vitamin B12 (Cobalamin)", "reference_range": null}, {"name": "Vitamin C (Ascorbic Acid)", "reference_range": null}, {"name": "Vitamin D", "reference_range": null}, {"name": "Vitamin E", "reference_range": null}, {"name": "Folate", "reference_range": null}]
Preparation
["Fast overnight for 8–12 hours.", "Stop all vitamin supplements 24 hours before collection.", "Protect blood tubes from light by wrapping in foil."]
Indications
["Suspected nutritional deficiency", "Monitoring supplementation efficacy", "Identifying potential vitamin toxicities", "Patients with malabsorption syndromes", "Individuals on restrictive diets"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 24319-7 ICD-10: E63.9
Clinical summary
This diagnostic test quantitatively evaluates levels of essential fat-soluble and water-soluble vitamins in serum.
TEST-3418
VMA (Vanillylmandelic Acid) Random Urine Test

This diagnostic test evaluates the level of vanillylmandelic acid (VMA) in a random urine sample to screen for neuroendocrine tumors.

Random Urine 2 working days after collection (report available Wed/Sat by 9 AM) 850.00 AED
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What it measures
["Vanillylmandelic Acid (VMA)", "Catecholamine Metabolites"]
Parameters
[{"name": "Vanillylmandelic Acid (VMA)", "reference_range": null}]
Preparation
["Strictly avoid theophylline, chocolate, vanilla, banana, alcoholic beverages, tea/coffee, tobacco, and strenuous exercise for exactly 72 hours before collection.", "Do not stop prescribed medication without consulting your doctor."]
Indications
["Screening for pheochromocytoma", "Screening for neuroblastoma", "Monitoring known neuroendocrine tumors", "Evaluating adrenal hyperactivity"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 3556-9 ICD-10: C74.1
Clinical summary
This diagnostic test evaluates the level of vanillylmandelic acid (VMA) in a random urine sample to screen for neuroendocrine tumors.
TEST-3114
Von Willebrand Factor (VWF) Gene Genetic Test

This test identifies pathogenic variants in the VWF gene associated with von Willebrand disease.

Peripheral whole blood (EDTA) or FTA card 3 – 4 Weeks 2,800.00 AED
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What it measures
["Pathogenic variants in the VWF gene", "Small nucleotide variants, insertions, deletions"]
Parameters
[]
Preparation
["No fasting required", "Inform genetic counselor about all current medications"]
Indications
["Individuals with unexplained bleeding", "Heavy menstrual bleeding", "Family history of VWD", "Pre-surgical evaluation with inconclusive standard coagulation tests"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 82652-2 ICD-10: D68.0
Clinical summary
This test identifies pathogenic variants in the VWF gene associated with von Willebrand disease.
TEST-4135
VPS13B Gene Cohen Syndrome Genetic Test

This test identifies pathogenic variants in the VPS13B gene, confirming a diagnosis of Cohen syndrome.

Whole blood (EDTA), FTA card, or extracted DNA 3–4 weeks from sample receipt 2,800.00 AED
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What it measures
["Pathogenic variants in the VPS13B gene", "Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)"]
Parameters
[]
Preparation
["No fasting required", "Genetic counseling session is mandatory prior to sample collection"]
Indications
["Clinical suspicion of Cohen syndrome", "Family history of Cohen syndrome", "Need for definitive molecular diagnosis"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 83112-3 ICD-10: Q87.89
Clinical summary
This test identifies pathogenic variants in the VPS13B gene, confirming a diagnosis of Cohen syndrome.
TEST-5678
VPS37A Gene SPG53 Genetic Test

This test identifies pathogenic variants in the VPS37A gene, confirming a diagnosis of hereditary spastic paraplegia type 53 (SPG53).

Peripheral whole blood (EDTA) or FTA card finger-prick 3–4 weeks 2,800.00 AED
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What it measures
["VPS37A gene pathogenic variants", "Copy Number Variants (CNVs) in VPS37A"]
Parameters
[]
Preparation
[]
Indications
["Suspected hereditary spastic paraplegia type 53 (SPG53)", "Family risk assessment for SPG53", "Guiding targeted management"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 21636-6 ICD-10: G11.4, G11.9
Clinical summary
This test identifies pathogenic variants in the VPS37A gene, confirming a diagnosis of hereditary spastic paraplegia type 53 (SPG53).
TEST-3226
VPS45 Gene Severe Congenital Neutropenia Type 5 Genetic Test

This test identifies pathogenic variants in the VPS45 gene associated with severe congenital neutropenia type 5.

Peripheral whole blood (EDTA), 3–5 mL; alternative: buccal swab or extracted DNA 3–4 weeks 2,800.00 AED
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What it measures
["VPS45 gene sequence", "Pathogenic variants"]
Parameters
[]
Preparation
["Mandatory genetic counseling session prior to sample collection", "Disclose all immunosuppressive medications", "Disclose recent G-CSF use", "Disclose history of stem cell transplantation"]
Indications
["Autosomal recessive severe congenital neutropenia type 5 (SCN5) caused by biallelic VPS45 mutations", "Persistent neutropenia of unknown cause", "Family history of severe congenital neutropenia"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 81369-6 ICD-10: D70.0
Clinical summary
This test identifies pathogenic variants in the VPS45 gene associated with severe congenital neutropenia type 5.
TEST-2382
WASHC5 Gene Ritscher‑Schinzel Syndrome Type 1 Genetic Test

This genetic test identifies pathogenic mutations in the WASHC5 gene, confirming Ritscher‑Schinzel syndrome type 1.

Peripheral whole blood 3–4 Weeks from sample receipt 2,800.00 AED
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What it measures
["Pathogenic variants in the WASHC5 gene"]
Parameters
[]
Preparation
[]
Indications
["Infants and children with clinical features suggestive of Ritscher‑Schinzel syndrome", "Family members of an index case for recurrence risk assessment"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 94473-0 ICD-10: Q87.89
Clinical summary
This genetic test identifies pathogenic mutations in the WASHC5 gene, confirming Ritscher‑Schinzel syndrome type 1.

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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