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

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Biochemistry test prices

Showing 256–270 of 1,113 matching tests.

Biochemistry diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-2411 Comprehensive Lipid Profile (Cardiovascular Risk Panel) Test This test evaluates multiple lipid components and clotting factors to assess cardiovascular risk.	Blood (Serum, Plasma)	Same Day (sample by 4 PM Monday to Saturday)	550.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Total Cholesterol", "HDL Cholesterol", "LDL Cholesterol", "Triglycerides", "Lipoprotein(a)", "Apolipoprotein A1", "Apolipoprotein B", "Fibrinogen Activity"] Parameters [{"name": "Total Cholesterol", "reference_range": null}, {"name": "HDL Cholesterol", "reference_range": null}, {"name": "LDL Cholesterol", "reference_range": null}, {"name": "Triglycerides", "reference_range": null}, {"name": "Lipoprotein(a)", "reference_range": null}, {"name": "Apolipoprotein A1", "reference_range": null}, {"name": "Apolipoprotein B", "reference_range": null}, {"name": "Fibrinogen Activity", "reference_range": null}] Preparation ["Fasting for at least 12 hours is required.", "Do not discontinue prescribed medications like statins or antihypertensives without consulting your physician."] Indications ["Cardiovascular risk screening", "Monitoring therapy efficacy (e.g., statins)", "Assessing hidden vascular inflammation and clotting tendencies"] Measurement technique Confirm with laboratory Codes LOINC: 24331-1 ICD-10: E78.5, Z13.220 Clinical summary This test evaluates multiple lipid components and clotting factors to assess cardiovascular risk.
TEST-2657 Comprehensive Newborn Screening Panel Test This test screens for over 50 inborn errors of metabolism using multiple analytical platforms.	Heel-prick capillary blood on filter paper (3 saturated spots)	Next day (samples Mon/Wed/Fri by 9 AM)	1,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Amino acid levels", "Acylcarnitine profiles", "Hormone markers", "Enzyme markers", "Hemoglobin variants"] Parameters [] Preparation ["Complete clinical details and comprehensive drug/supplement history must accompany the sample.", "Maternal medications (if breastfeeding) must be reported.", "Do not discontinue prescribed medications without consulting a physician."] Indications ["Routine newborn screening", "Screening for inherited metabolic disorders"] Measurement technique Confirm with laboratory Codes LOINC: 57732-8 ICD-10: Z13.21 Clinical summary This test screens for over 50 inborn errors of metabolism using multiple analytical platforms.
TEST-2813 Comprehensive Osteoporosis Panel Test This diagnostic test evaluates key markers related to bone metabolism and calcium homeostasis to assess bone health and osteoporosis risk.	Serum	Same Day (if sample received by 4 PM Mon)	1,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Calcium", "Phosphorus", "Alkaline Phosphatase", "25-Hydroxy Vitamin D", "Intact Parathyroid Hormone (PTH)", "Bone Metabolism Markers"] Parameters [{"name": "Calcium", "reference_range": null}, {"name": "Phosphorus", "reference_range": null}, {"name": "Alkaline Phosphatase", "reference_range": null}, {"name": "25-Hydroxy Vitamin D", "reference_range": null}, {"name": "Intact Parathyroid Hormone", "reference_range": null}] Preparation ["Fasting between 8–10 AM is mandatory", "Collect blood between 8–10 AM"] Indications ["Screening for osteoporosis", "Monitoring osteoporosis treatment", "Evaluating fracture risk", "Investigating metabolic bone disease"] Measurement technique Confirm with laboratory Codes LOINC: 58410-2 ICD-10: M81.0 Clinical summary This diagnostic test evaluates key markers related to bone metabolism and calcium homeostasis to assess bone health and osteoporosis risk.
TEST-1750 Congenital Adrenal Hyperplasia (CAH) Full Gene Sequence Analysis Test This test performs full-gene sequencing of the CYP21A2 gene to identify mutations causing Congenital Adrenal Hyperplasia (CAH).	Peripheral whole blood (3–5 mL in EDTA lavender-top tube); alternative: extracted genomic DNA (2 µg minimum)	4–5 weeks	2,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["CYP21A2 gene sequence", "Pathogenic variants", "Copy number variants"] Parameters [] Preparation ["No fasting required", "No medication adjustment necessary", "Inform physician about current corticosteroid use", "Valid doctor's prescription required (except for approved exemptions)", "Informed consent must be signed"] Indications ["Neonatal screening follow-up", "Ambiguous genitalia", "Salt-wasting crises", "Precocious puberty in boys", "Hirsutism with oligomenorrhea in females", "Carrier testing in at-risk relatives", "Pre-surgical clearance", "Pregnancy-related screening", "Travel abroad"] Measurement technique Confirm with laboratory Codes LOINC: 21631-4 ICD-10: E25.0, E25.8, E25.9 Clinical summary This test performs full-gene sequencing of the CYP21A2 gene to identify mutations causing Congenital Adrenal Hyperplasia (CAH).
TEST-706 Connexin 26 Mutation Detection Test This test identifies pathogenic variants in the GJB2 gene, the most common genetic cause of congenital sensorineural hearing loss.	Whole blood (4 mL lavender-top EDTA tube)	13 working days (sample by 11 am Saturday)	1,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the GJB2 gene", "Connexin 26 protein encoding sequence"] Parameters [] Preparation [] Indications ["Diagnosis of congenital sensorineural hearing loss", "Carrier screening for prospective parents", "Prenatal diagnosis (with CVS or amniocentesis)", "Genetic counseling for families with hearing loss"] Measurement technique Confirm with laboratory Codes LOINC: 21679-8 ICD-10: H90.3 Clinical summary This test identifies pathogenic variants in the GJB2 gene, the most common genetic cause of congenital sensorineural hearing loss.
TEST-700 Connexin 30 (GJB6) Mutation Detection Test This test detects pathogenic variants in the GJB6 gene, a common cause of congenital deafness.	Whole blood	10 working days	1,100.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["GJB6 gene deletions", "GJB6 gene sequence variants"] Parameters [] Preparation [] Indications ["Newborns with failed OAE screening", "Children with delayed speech", "Adults with familial deafness"] Measurement technique Confirm with laboratory Codes LOINC: 21663-7 ICD-10: H90.3 Clinical summary This test detects pathogenic variants in the GJB6 gene, a common cause of congenital deafness.
TEST-5811 COQ8A Gene Spinocerebellar Ataxia Type 9 (Autosomal Recessive) Genetic Test This genetic test identifies pathogenic variants in the COQ8A gene associated with autosomal recessive spinocerebellar ataxia type 9 (SCAR9).	Whole blood (EDTA) or FTA card (finger-prick)	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 COQ8A gene", "Presence of mutations causing SCAR9"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of any medications"] Indications ["Clinical suspicion of autosomal recessive spinocerebellar ataxia type 9 (SCAR9)", "Family history of SCAR9", "Progressive cerebellar ataxia of unknown origin"] Measurement technique Confirm with laboratory Codes LOINC: 82939-0 ICD-10: G11.1, G11.8, E71.540 Clinical summary This genetic test identifies pathogenic variants in the COQ8A gene associated with autosomal recessive spinocerebellar ataxia type 9 (SCAR9).
TEST-3584 COQ8B Gene Nephrotic Syndrome Type 9 Genetic Testing (NGS) Test This test detects pathogenic variants in the COQ8B gene associated with steroid-resistant nephrotic syndrome.	Peripheral whole blood (5 mL EDTA)	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 COQ8B gene"] Parameters [] Preparation [] Indications ["Diagnosis of steroid-resistant nephrotic syndrome type 9", "Familial screening for COQ8B variants", "Guiding targeted management"] Measurement technique Confirm with laboratory Codes LOINC: 21633-8 ICD-10: N04.9 Clinical summary This test detects pathogenic variants in the COQ8B gene associated with steroid-resistant nephrotic syndrome.
TEST-3421 CORIN Gene Preeclampsia/Eclampsia Type 5 Genetic Test This genetic test identifies pathogenic variants in the CORIN gene associated with an increased risk of developing severe, early-onset preeclampsia type 5 during pregnancy.	Peripheral Whole Blood	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 CORIN gene", "Disruption of atrial natriuretic peptide conversion"] Parameters [] Preparation ["Genetic counselling session required prior to sample collection", "No fasting required"] Indications ["Assessment of genetic risk for severe, early-onset preeclampsia type 5", "Guiding antenatal surveillance strategies"] Measurement technique Confirm with laboratory Codes LOINC: 95382-6 ICD-10: O14.9, O15.0, Z15.89 Clinical summary This genetic test identifies pathogenic variants in the CORIN gene associated with an increased risk of developing severe, early-onset preeclampsia type 5 during pregnancy.
TEST-709 Corticosterone Test This diagnostic test evaluates adrenal function by measuring the level of the hormone corticosterone in the blood.	Serum (1 mL) or Plasma (heparin)	3–5 business days (reports issued Wednesday and Saturday for Monday/Thursday draws)	550.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Corticosterone levels", "Adrenal function", "Stress response", "Circadian rhythm integrity"] Parameters [{"name": "Corticosterone", "reference_range": null}] Preparation ["Fasting overnight (8-10 hours)", "Temporarily stopping steroid drugs (consult physician)", "Strict adherence to draw time (8-10 AM or 4-6 PM)", "Use red-top tube only"] Indications ["Suspected adrenal insufficiency", "Suspected Cushing's syndrome", "Monitoring anti-aging protocols", "Monitoring sports performance protocols", "Evaluation of stress response"] Measurement technique Confirm with laboratory Codes LOINC: 2141-0 ICD-10: E27.8 Clinical summary This diagnostic test evaluates adrenal function by measuring the level of the hormone corticosterone in the blood.
TEST-713 Cortisol Free Serum Test This diagnostic test evaluates adrenal function by measuring the level of biologically active, unbound cortisol in the serum.	Serum	2–3 weeks	2,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Biologically active, unbound cortisol", "Adrenal function"] Parameters [{"name": "Free Cortisol", "reference_range": null}] Preparation ["Fasting is not mandatory.", "Inform phlebotomist about all medications, supplements (especially biotin), and recent corticosteroid use."] Indications ["Diagnosis of Cushing's syndrome", "Diagnosis of adrenal insufficiency", "Evaluation during pregnancy", "Evaluation during oral contraceptive use"] Measurement technique Confirm with laboratory Codes LOINC: 14634-3 ICD-10: E27.9 Clinical summary This diagnostic test evaluates adrenal function by measuring the level of biologically active, unbound cortisol in the serum.
TEST-727 Cortisone (Compound E) 24-Hour Urine Test This diagnostic test evaluates the total amount of cortisone excreted in the urine over a 24-hour period. It is considered the gold standard for quantifying cortisone levels.	24-Hour Urine (with boric acid preservative)	2–3 weeks	4,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Total urinary cortisone excretion", "Adrenal gland function"] Parameters [{"name": "Cortisone (Compound E)", "reference_range": null}] Preparation ["Collect all urine over a full 24-hour period in the provided container.", "Keep the sample refrigerated throughout the collection period.", "Note the total volume collected."] Indications ["Suspected Cushing’s syndrome", "Suspected adrenal insufficiency", "Monitoring adrenal disorders", "Evaluation of endocrine function"] Measurement technique Confirm with laboratory Codes LOINC: 27135-4 ICD-10: E24.9 Clinical summary This diagnostic test evaluates the total amount of cortisone excreted in the urine over a 24-hour period. It is considered the gold standard for quantifying cortisone levels.
TEST-4312 COX10 Gene Genetic Test for Mitochondrial Encephalopathy with Proximal Renal Tubulopathy This genetic test evaluates the COX10 gene for pathogenic variants associated with mitochondrial encephalopathy and proximal renal tubulopathy.	Peripheral Whole Blood (EDTA)	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 COX10 gene", "Single nucleotide changes", "Small insertions/deletions", "Copy number alterations"] Parameters [] Preparation ["Inform the team of all medications, especially anticoagulants", "Pre-test genetic counselling session is mandatory"] Indications ["Patients with neurological and renal symptoms suggestive of this rare disorder", "Confirmation of clinical diagnosis", "Family screening"] Measurement technique Confirm with laboratory Codes LOINC: 93353-6 ICD-10: G31.81, N19 Clinical summary This genetic test evaluates the COX10 gene for pathogenic variants associated with mitochondrial encephalopathy and proximal renal tubulopathy.
TEST-6160 CPT1A Gene (Carnitine Palmitoyltransferase 1A Deficiency) Genetic Test This genetic test identifies pathogenic variants in the CPT1A gene, which are responsible for carnitine palmitoyltransferase 1A deficiency, a fatty acid oxidation disorder.	Whole Blood (EDTA), Buccal Swab, or DNA on FTA Card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["CPT1A gene variants", "Long-chain fatty acid oxidation pathway"] Parameters [] Preparation ["No fasting required", "Inform phlebotomist about anticoagulant therapy"] Indications ["Unexplained metabolic decompensation", "Family history of CPT1A deficiency", "Carrier screening", "Reproductive planning"] Measurement technique Confirm with laboratory Codes LOINC: 94706-2 ICD-10: E71.314 Clinical summary This genetic test identifies pathogenic variants in the CPT1A gene, which are responsible for carnitine palmitoyltransferase 1A deficiency, a fatty acid oxidation disorder.
TEST-6065 CPT2 Gene Carnitine Palmitoyltransferase II Deficiency (Lethal Neonatal) Genetic Test This genetic test identifies pathogenic variants in the CPT2 gene associated with lethal neonatal carnitine palmitoyltransferase II deficiency.	Whole Blood (Venous), Extracted DNA, 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 ["CPT2 gene sequence", "Copy Number Variations (CNVs) in CPT2 gene"] Parameters [] Preparation ["Inform phlebotomist of all current medications", "Do not discontinue prescribed medication without consulting physician"] Indications ["Suspected lethal neonatal CPT2 deficiency", "Neonatal metabolic crisis", "Family history of CPT2 deficiency"] Measurement technique Confirm with laboratory Codes LOINC: 101675-7 ICD-10: E71.312 Clinical summary This genetic test identifies pathogenic variants in the CPT2 gene associated with lethal neonatal carnitine palmitoyltransferase II deficiency.

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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Biochemistry tests in Dubai & UAE

Biochemistry test prices

Biochemistry: overview

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