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 1066–1080 of 1,113 matching tests.

Biochemistry diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-3513 UNC45B Gene Cataract Type 43 Genetic Test This genetic test identifies pathogenic variants in the UNC45B gene associated with autosomal dominant congenital cataract type 43.	Peripheral whole blood, FTA card, or extracted DNA	18 – 21 working days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the UNC45B gene", "Complete coding region of UNC45B"] Parameters [] Preparation ["No specific fasting required", "No specific medication or diet restrictions"] Indications ["Diagnosis of autosomal dominant congenital cataract type 43", "Genetic counselling for families with congenital cataracts"] Measurement technique Confirm with laboratory Codes LOINC: 101188-5 ICD-10: Q12.0 Clinical summary This genetic test identifies pathogenic variants in the UNC45B gene associated with autosomal dominant congenital cataract type 43.
TEST-4902 UNG Gene Immunodeficiency Type 5 with Hyper-IgM (Genetic Test) This genetic test analyzes the UNG gene for pathogenic variants associated with Immunodeficiency Type 5 with Hyper-IgM syndrome.	Peripheral whole blood, 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 UNG gene", "Copy number variants (CNVs) in the UNG gene"] Parameters [] Preparation [] Indications ["Suspected Immunodeficiency Type 5 with Hyper-IgM syndrome", "Family history of primary immunodeficiency", "Carrier screening"] Measurement technique Confirm with laboratory Codes LOINC: 32387-5 ICD-10: D82.4 Clinical summary This genetic test analyzes the UNG gene for pathogenic variants associated with Immunodeficiency Type 5 with Hyper-IgM syndrome.
TEST-5013 UPF3B Gene Mental Retardation, X-linked Type 14 (Genetic Test) This diagnostic test evaluates the UPF3B gene for pathogenic variants associated with X-linked intellectual disability type 14 (MRX14). It utilizes Next-Generation Sequencing (NGS)...	Whole Blood (EDTA) 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 UPF3B gene", "Full coding region and splice-site coverage"] Parameters [{"name": "Diagnostic Sensitivity", "reference_range": "99.9% (complete coding region + splice sites)"}, {"name": "Methodology", "reference_range": "Next-Generation Sequencing (Illumina platform, 1000x depth)"}, {"name": "ACMG Variant Interpretation", "reference_range": "Full clinical classification with ≥2 genetic counselors review"}] Preparation ["No specific fasting required.", "No medication or diet restrictions unless advised by your physician."] Indications ["Diagnosis of X-linked intellectual disability type 14 (MRX14)", "Establishing recurrence risk in families", "Guiding early intervention strategies"] Measurement technique Confirm with laboratory Codes LOINC: 81768-4 ICD-10: F79, Z13.89, Z14.8 Clinical summary This diagnostic test evaluates the UPF3B gene for pathogenic variants associated with X-linked intellectual disability type 14 (MRX14). It utilizes Next-Generation Sequencing (NGS) to analyze the entire coding region and splice sites.
TEST-3344 Urea Cycle Disorder Panel Test This diagnostic test evaluates the levels of amino acids and related metabolites in plasma and urine to identify potential urea cycle disorders.	Urine + Plasma	5 working days	1,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Plasma amino acids", "Urinary orotic acid", "Urea cycle intermediates (citrulline, argininosuccinate)"] Parameters [{"name": "Plasma Amino Acids", "reference_range": null}, {"name": "Urinary Orotic Acid", "reference_range": null}, {"name": "Plasma Citrulline", "reference_range": null}, {"name": "Plasma Argininosuccinate", "reference_range": null}] Preparation ["Do not discontinue prescribed medication without consulting your doctor", "Provide a complete drug history at the time of sample collection"] Indications ["Suspected inborn error of the urea cycle", "Evaluation of hyperammonemia", "Screening for citrullinemia, argininosuccinic aciduria, arginase deficiency, ornithine transcarbamylase deficiency"] Measurement technique Confirm with laboratory Codes LOINC: 34531-1 ICD-10: E72.2 Clinical summary This diagnostic test evaluates the levels of amino acids and related metabolites in plasma and urine to identify potential urea cycle disorders.
TEST-4644 UROD Gene Porphyria Cutanea Tarda (PCT) Genetic Test This test evaluates the UROD gene for pathogenic variants associated with Porphyria Cutanea Tarda (PCT). It helps determine if the condition is inherited (familial) or acquired/spo...	Whole Blood (EDTA), Extracted DNA, or FTA Card	3–4 weeks (express available)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the UROD gene", "Presence of single-nucleotide variants, small deletions, and duplications"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication without consulting your doctor"] Indications ["Suspected familial Porphyria Cutanea Tarda (PCT)", "Differentiation between familial and acquired PCT", "Family screening for PCT"] Measurement technique Confirm with laboratory Codes LOINC: 90777-8 ICD-10: E80.1 Clinical summary This test evaluates the UROD gene for pathogenic variants associated with Porphyria Cutanea Tarda (PCT). It helps determine if the condition is inherited (familial) or acquired/sporadic.
TEST-6230 USF1 Gene Hyperlipidemia, Familial Combined Susceptibility Test This test evaluates the USF1 gene for pathogenic variants linked to familial combined hyperlipidemia.	Whole Blood (Peripheral)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["USF1 gene pathogenic variants", "Inherited risk for hyperlipidemia"] Parameters [] Preparation ["No specific fasting required", "Avoid recent blood transfusion (wait 4 weeks)"] Indications ["Family history of premature cardiovascular disease", "Elevated cholesterol and triglycerides", "Screening for inherited hyperlipidemia risk"] Measurement technique Confirm with laboratory Codes LOINC: 92606-2 ICD-10: E78.49 Clinical summary This test evaluates the USF1 gene for pathogenic variants linked to familial combined hyperlipidemia.
TEST-2747 Usher Syndrome NGS & Sanger Testing Test This diagnostic test evaluates for pathogenic variants in genes associated with Usher syndrome, a genetic disorder causing progressive vision loss and hearing impairment.	Whole blood	45 working days	3,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in Usher syndrome genes", "Genetic mutations causing dual sensory loss"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication"] Indications ["Suspected Usher syndrome", "Progressive hearing loss and vision loss", "Family history of Usher syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Q87.8 Clinical summary This diagnostic test evaluates for pathogenic variants in genes associated with Usher syndrome, a genetic disorder causing progressive vision loss and hearing impairment.
TEST-3373 Vancomycin Test (Therapeutic Drug Monitoring) This test measures the lowest concentration of vancomycin in the blood just before the next dose (trough level). It helps optimize dosing to ensure effectiveness and minimize toxic...	Serum	Same Day (sample received by 4 PM)	900.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Vancomycin serum concentration", "Trough level"] Parameters [{"name": "Vancomycin", "reference_range": "10–20 mg/L"}] Preparation ["No fasting required", "Sample must be collected exactly 30 minutes before the next scheduled vancomycin infusion"] Indications ["Monitoring vancomycin therapy", "Suspected vancomycin toxicity", "Adjusting vancomycin dosage"] Measurement technique Confirm with laboratory Codes LOINC: 4103-0 ICD-10: Z51.81, Z16.21, T36.8X5A Clinical summary This test measures the lowest concentration of vancomycin in the blood just before the next dose (trough level). It helps optimize dosing to ensure effectiveness and minimize toxicity.
TEST-3430 Vanillylmandelic Acid (VMA) 24-Hour Urine Test This diagnostic test evaluates the levels of vanillylmandelic acid (VMA) in a 24-hour urine collection to screen for catecholamine-secreting tumours.	24-Hour Urine Collection	2 business days from sample receipt	850.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Vanillylmandelic Acid (VMA)", "Catecholamine metabolism"] Parameters [{"name": "Vanillylmandelic Acid (VMA)", "reference_range": null}] Preparation ["Strictly avoid theophylline-containing medications, chocolate, vanilla, bananas, alcohol, coffee, tea, tobacco products, and strenuous physical exercise for 72 hours before and during the entire collection period.", "Do not discontinue prescribed medication without consulting your physician."] Indications ["Screening for neuroblastoma in children", "Screening for pheochromocytoma in adults", "Investigation of suspected catecholamine-secreting tumours"] Measurement technique Confirm with laboratory Codes LOINC: 13950-7 ICD-10: C74.10, Z12.89 Clinical summary This diagnostic test evaluates the levels of vanillylmandelic acid (VMA) in a 24-hour urine collection to screen for catecholamine-secreting tumours.
TEST-3386 Very Long Chain Fatty Acids (VLCFA) Test This diagnostic test evaluates the levels of specific very long chain fatty acids (C22:0, C24:0, C26:0) and their ratios in serum to screen for peroxisomal disorders.	Serum (Peripheral Blood)	2–3 weeks (sample by 7th of the month)	4,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["C22:0", "C24:0", "C26:0", "C26:0/C22:0 ratio"] Parameters [{"name": "C22:0", "reference_range": null}, {"name": "C24:0", "reference_range": null}, {"name": "C26:0", "reference_range": null}, {"name": "C26:0/C22:0 Ratio", "reference_range": null}] Preparation ["Overnight fasting is mandatory for adults.", "Pediatric patients need not fast but sample must be drawn before the next meal or scheduled feeding.", "Avoid alcohol for 24 hours prior to collection.", "Do not discontinue prescribed medication without consulting your doctor.", "Avoid holding or changing anti-epileptics, adrenal steroids, or dietary therapy before the test."] Indications ["Suspected peroxisomal biogenesis disorders", "Suspected X-linked adrenoleukodystrophy", "Suspected Zellweger spectrum syndromes", "Neonatal screening follow-up", "Family history of peroxisomal disorders"] Measurement technique Confirm with laboratory Codes LOINC: 10201-7 ICD-10: E71.3 Clinical summary This diagnostic test evaluates the levels of specific very long chain fatty acids (C22:0, C24:0, C26:0) and their ratios in serum to screen for peroxisomal disorders.
TEST-5394 VIPAS39 Gene NGS Test This test identifies pathogenic variants in the VIPAS39 gene associated with Arthrogryposis, Renal dysfunction, and Cholestasis (ARC) syndrome type 2.	Peripheral whole blood or buccal swab	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 VIPAS39 gene", "Copy number variants in the VIPAS39 gene"] Parameters [] Preparation ["No fasting required", "No medication changes required"] Indications ["Clinical suspicion of ARC syndrome type 2", "Infants presenting with arthrogryposis, renal dysfunction, and cholestasis"] Measurement technique Confirm with laboratory Codes LOINC: 81260-5 ICD-10: Q87.8 Clinical summary This test identifies pathogenic variants in the VIPAS39 gene associated with Arthrogryposis, Renal dysfunction, and Cholestasis (ARC) syndrome type 2.
TEST-3422 Vitamin A (Retinol) Test This diagnostic test evaluates serum retinol levels to assess Vitamin A status and identify potential deficiency or toxicity.	Serum (peripheral whole blood)	4 Business Days from sample pickup	950.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Serum Retinol Level"] Parameters [{"name": "Serum Retinol", "reference_range": null}] Preparation ["Fast overnight", "Avoid vitamin A supplements for 24 hours prior to collection"] Indications ["Suspected Vitamin A deficiency", "Suspected Vitamin A toxicity", "Monitoring retinol-based therapy", "Evaluation of malabsorption syndromes", "Assessment in patients with chronic liver disease"] Measurement technique Confirm with laboratory Codes LOINC: 74797-6 ICD-10: E50.9, E67.0 Clinical summary This diagnostic test evaluates serum retinol levels to assess Vitamin A status and identify potential deficiency or toxicity.
TEST-3411 Vitamin B1 (Thiamine Pyrophosphate) Blood Test This diagnostic test evaluates the level of active thiamine pyrophosphate (TPP) in whole blood.	Whole Blood	3 – 5 business days	1,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Active Thiamine Pyrophosphate (TPP)", "Vitamin B1 Coenzyme Activity"] Parameters [{"name": "Thiamine Pyrophosphate (TPP)", "reference_range": null}] Preparation ["No fasting required", "Sample must be shielded from light immediately after collection"] Indications ["Investigating peripheral neuropathy", "Investigating metabolic encephalopathy", "Investigating unexplained cardiac failure", "Suspected nutritional malabsorption", "Evaluation of thiamine status"] Measurement technique Confirm with laboratory Codes LOINC: 4811-0 ICD-10: E51.9 Clinical summary This diagnostic test evaluates the level of active thiamine pyrophosphate (TPP) in whole blood.
TEST-3426 Vitamin B1 (Thiamine) Test This diagnostic test evaluates the concentration of thiamine (Vitamin B1) in the blood to identify deficiency.	Serum/Plasma	2–3 weeks	850.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Thiamine concentration", "Nutritional status"] Parameters [{"name": "Thiamine", "reference_range": null}] Preparation ["Overnight fasting (10-12 hours) is strictly required.", "Inform phlebotomist of medications affecting thiamine metabolism."] Indications ["Chronic alcoholism", "Malabsorption syndromes", "High metabolic demand", "Pre-bariatric surgery screening"] Measurement technique Confirm with laboratory Codes LOINC: 32362-9 ICD-10: E53.8 Clinical summary This diagnostic test evaluates the concentration of thiamine (Vitamin B1) in the blood to identify deficiency.
TEST-3393 Vitamin B12 Binding Capacity (Unsaturated Transcobalamin) Test This diagnostic test evaluates the functional status of vitamin B12 at the tissue level by measuring the unbound fraction of transcobalamin.	Serum (peripheral venous blood)	2–3 weeks (send-out batch to specialized reference laboratory)	2,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Unbound transcobalamin", "Functional vitamin B12 availability"] Parameters [{"name": "Unsaturated Transcobalamin Binding Capacity", "reference_range": null}] Preparation ["Fasting for 8 to 10 hours prior to blood draw is recommended", "Inform phlebotomist about all supplements, especially biotin", "Follow physician's specific instructions"] Indications ["Suspected functional B12 deficiency despite normal serum B12 levels", "Evaluation of neurological or haematological symptoms potentially related to B12 deficiency", "Monitoring response to B12 therapy"] Measurement technique Confirm with laboratory Codes LOINC: 13956-1 ICD-10: E53.8 Clinical summary This diagnostic test evaluates the functional status of vitamin B12 at the tissue level by measuring the unbound fraction of transcobalamin.

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.

Before booking

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.

Explore this area

Biochemistry tests in Dubai & UAE

Biochemistry test prices

Biochemistry: overview

Use the test details as a conversation starter

Related Biochemistry categories