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 301–315 of 1,113 matching tests.

Biochemistry diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-988 Dexamethasone Therapeutic Drug Monitoring Test This test measures the concentration of dexamethasone in the blood serum to guide therapeutic dosing.	Serum	2–3 weeks	1,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Serum Dexamethasone Concentration"] Parameters [{"name": "Serum Dexamethasone", "reference_range": null}] Preparation ["Fasting serum sample required", "Sample collection between 8–10 AM", "Use red-top tube (no SST gel)", "Keep specimen refrigerated or frozen immediately"] Indications ["Patients on long-term or high-dose corticosteroid therapy", "Management of inflammatory conditions", "Management of autoimmune conditions", "Management of adrenal insufficiency", "Anti-aging protocols involving corticosteroids"] Measurement technique Confirm with laboratory Codes LOINC: 19633-6 ICD-10: Z51.81 Clinical summary This test measures the concentration of dexamethasone in the blood serum to guide therapeutic dosing.
TEST-992 DHEA Stimulation Test (ACTH Stimulation) This test evaluates adrenal gland reserve by measuring DHEA response to synthetic ACTH stimulation.	Serum (Peripheral Blood)	Same Day (sample drawn Tue/Fri by 9 AM)	1,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["DHEA levels at baseline", "DHEA levels 90 minutes post-ACTH stimulation", "Adrenal gland reserve"] Parameters [{"name": "DHEA Baseline", "reference_range": null}, {"name": "DHEA Post-Stimulation (90 min)", "reference_range": null}, {"name": "Delta DHEA", "reference_range": null}] Preparation ["Overnight fasting of 10–12 hours is mandatory; only water is permitted.", "Do not discontinue prescribed corticosteroids, estrogen therapy, or DHEA supplements without consulting your doctor.", "Apply no creams or lotions to your arms on the day of collection."] Indications ["Diagnosing subtle or partial adrenal insufficiency", "Diagnosing adult-onset congenital adrenal hyperplasia", "Guiding anti-aging and hormone optimization protocols"] Measurement technique Confirm with laboratory Codes LOINC: 28620-4 ICD-10: E27.1, E27.2, E24.0 Clinical summary This test evaluates adrenal gland reserve by measuring DHEA response to synthetic ACTH stimulation.
TEST-3721 DHH Gene Mutation Analysis for 46,XY Gonadal Dysgenesis & Minifascicular Neuropathy Test This diagnostic test evaluates the DHH gene for pathogenic variants associated with 46,XY gonadal dysgenesis and minifascicular neuropathy.	Peripheral Whole Blood, Serum, or Plasma	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 DHH gene", "Coding exons and intron-exon boundaries"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any anticoagulant therapy"] Indications ["Suspected 46,XY gonadal dysgenesis", "Suspected minifascicular neuropathy", "Family history of DHH-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 50396-0 ICD-10: Q99.1, G60.0 Clinical summary This diagnostic test evaluates the DHH gene for pathogenic variants associated with 46,XY gonadal dysgenesis and minifascicular neuropathy.
TEST-6010 DHTKD1 Gene Analysis (2-Aminoadipic 2-Oxoadipic Aciduria) Test This test identifies pathogenic variants in the DHTKD1 gene associated with 2-aminoadipic 2-oxoadipic aciduria.	Whole Blood (EDTA), 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 DHTKD1 gene"] Parameters [] Preparation ["Do not discontinue prescribed medication without physician instruction", "Pre-test genetic counseling session required"] Indications ["Suspected 2-aminoadipic 2-oxoadipic aciduria", "Family history of the disorder", "Confirmation following suggestive biochemical screening"] Measurement technique Confirm with laboratory Codes LOINC: 81261-8 ICD-10: E72.52 Clinical summary This test identifies pathogenic variants in the DHTKD1 gene associated with 2-aminoadipic 2-oxoadipic aciduria.
TEST-986 Diabetes Panel 2 Test This diagnostic test evaluates glycemic control and early renal function related to diabetes.	Fasting venous blood & first-morning urine	Same Day (reported by 9 PM)	550.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Fasting Plasma Glucose", "Two-hour Postprandial Glucose", "Glycated Hemoglobin (HbA1c)", "Urine Glucose", "Urine Ketones", "Urine Microalbumin"] Parameters [{"name": "Fasting Glucose", "reference_range": null}, {"name": "Postprandial Glucose", "reference_range": null}, {"name": "HbA1c", "reference_range": null}, {"name": "Urine Glucose", "reference_range": null}, {"name": "Urine Ketones", "reference_range": null}, {"name": "Urine Microalbumin", "reference_range": null}] Preparation ["Strict 12-hour overnight fasting required.", "Water is permitted in small sips only.", "Do not discontinue prescribed antidiabetic medication unless directed by your physician."] Indications ["Screening for diabetes", "Diagnosis of diabetes", "Monitoring glycemic control in known diabetics", "Assessment of early renal involvement"] Measurement technique Confirm with laboratory Codes LOINC: 51992-3 ICD-10: R73.09 Clinical summary This diagnostic test evaluates glycemic control and early renal function related to diabetes.
TEST-1003 Diazepam Blood Level Test (TDM) This diagnostic test evaluates the concentration of diazepam and its metabolites in the patient's serum or plasma.	Peripheral Serum or Plasma	2–3 weeks	2,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Serum Diazepam", "Diazepam Metabolites"] Parameters [{"name": "Diazepam", "reference_range": null}, {"name": "Nordiazepam (Desmethyldiazepam)", "reference_range": null}, {"name": "Temazepam", "reference_range": null}, {"name": "Oxazepam", "reference_range": null}] Preparation ["Schedule blood draw just before next scheduled dose (trough level)", "Continue all medications as prescribed", "Bring completed consent form"] Indications ["Long-term benzodiazepine therapy", "Suspected toxicity or non-adherence", "Dosage adjustments", "Monitoring drug interactions"] Measurement technique Confirm with laboratory Codes LOINC: 3948-7 ICD-10: Z51.81 Clinical summary This diagnostic test evaluates the concentration of diazepam and its metabolites in the patient's serum or plasma.
TEST-993 Digitoxin Test (Therapeutic Drug Monitoring) This test measures the concentration of digitoxin in the blood serum to monitor therapeutic levels and prevent toxicity.	Serum	2-3 weeks	2,600.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Serum digitoxin concentration"] Parameters [{"name": "Digitoxin", "reference_range": null}] Preparation ["Fast for at least 4 hours", "Schedule blood draw just before next scheduled dose", "Bring mandatory consent form"] Indications ["Monitoring digitoxin therapy", "Assessing risk of digitalis toxicity", "Patients with heart failure or atrial fibrillation on digitoxin"] Measurement technique Confirm with laboratory Codes LOINC: 3352-0 ICD-10: Z51.81 Clinical summary This test measures the concentration of digitoxin in the blood serum to monitor therapeutic levels and prevent toxicity.
TEST-1015 Disopyramide Drug Level Monitoring Test This diagnostic test evaluates the serum concentration of disopyramide to guide therapeutic dosing.	Serum	2–3 weeks after sample receipt by the 7th of the month	1,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Serum Disopyramide Concentration"] Parameters [{"name": "Disopyramide", "reference_range": null}] Preparation ["No fasting required", "Inform phlebotomist about all medications", "Sign Test Send Out Consent Form (Form 35)"] Indications ["Monitoring therapy for cardiac arrhythmias", "Assessing potential drug toxicity", "Optimizing disopyramide dosage"] Measurement technique Confirm with laboratory Codes LOINC: 3395-7 ICD-10: Z51.81 Clinical summary This diagnostic test evaluates the serum concentration of disopyramide to guide therapeutic dosing.
TEST-5907 DLAT Gene (Pyruvate Dehydrogenase E2 Deficiency) Genetic Test This genetic test identifies pathogenic variants in the DLAT gene associated with Pyruvate Dehydrogenase E2 Deficiency.	Peripheral Whole Blood / FTA Card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["DLAT gene sequence variants", "Pathogenic mutations in coding exons and flanking intronic regions"] Parameters [] Preparation ["No fasting required", "No medication change required", "Mandatory pre-genetic counselling session"] Indications ["Suspected Pyruvate Dehydrogenase E2 Deficiency", "Family history of metabolic disorders", "Unexplained neurological symptoms"] Measurement technique Confirm with laboratory Codes LOINC: 94248-9 ICD-10: E74.4 Clinical summary This genetic test identifies pathogenic variants in the DLAT gene associated with Pyruvate Dehydrogenase E2 Deficiency.
TEST-6037 DLD Gene Maple Syrup Urine Disease Type 3 Genetic Test This test evaluates the DLD gene for pathogenic variants associated with Maple Syrup Urine Disease Type 3.	Peripheral Whole Blood (Venous)	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 DLD gene", "Branched-chain amino acid metabolism disorder"] Parameters [] Preparation [] Indications ["Suspected Maple Syrup Urine Disease Type 3", "Carrier screening for family planning", "Diagnosis in symptomatic individuals"] Measurement technique Confirm with laboratory Codes LOINC: 86900-3 ICD-10: E71.0 Clinical summary This test evaluates the DLD gene for pathogenic variants associated with Maple Syrup Urine Disease Type 3.
TEST-4508 DLX3 Gene Trichodentoosseous Syndrome Genetic Test This test evaluates the DLX3 gene for mutations associated with Trichodentoosseous Syndrome (TDO). It identifies pathogenic variants causing hair, dental, and bone abnormalities.	Peripheral Whole Blood or FTA Card Spot	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["DLX3 gene sequence", "Single nucleotide variants", "Small insertions/deletions"] Parameters [] Preparation ["No fasting required", "No medication cessation required"] Indications ["Suspected Trichodentoosseous Syndrome", "Family history of TDO", "Carrier screening for at-risk relatives", "Reproductive planning"] Measurement technique Confirm with laboratory Codes LOINC: 21637-8 ICD-10: Q87.8 Clinical summary This test evaluates the DLX3 gene for mutations associated with Trichodentoosseous Syndrome (TDO). It identifies pathogenic variants causing hair, dental, and bone abnormalities.
TEST-2275 DLX5 Gene Split-Hand/Foot Malformation Type 1 with Sensorineural Hearing Loss Genetic Test This genetic test evaluates the DLX5 gene for pathogenic mutations linked to Split-Hand/Foot Malformation Type 1 and sensorineural hearing loss.	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 mutations in the DLX5 gene", "Coding regions and splice sites of DLX5"] Parameters [] Preparation ["Pre-test genetic counseling session is mandatory.", "Informed consent must be documented."] Indications ["Diagnosis of Split-Hand/Foot Malformation Type 1 (SHFM1)", "Diagnosis of sensorineural hearing loss associated with DLX5 mutations", "Genetic counseling for families with a history of SHFM1 or related hearing loss"] Measurement technique Confirm with laboratory Codes LOINC: 93711-0 ICD-10: Q71.6, Q72.5, Q73.8, H90.3 Clinical summary This genetic test evaluates the DLX5 gene for pathogenic mutations linked to Split-Hand/Foot Malformation Type 1 and sensorineural hearing loss.
TEST-1636 DMD/BMD Mutation Screening (26 Exons) Test This test screens for common deletions and duplications within the 26 exons of the DMD gene, associated with Duchenne and Becker muscular dystrophies.	Amniotic fluid or chorionic villus sampling	4–5 business days	1,400.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Deletions in DMD gene exons", "Duplications in DMD gene exons"] Parameters [] Preparation [] Indications ["Family history of DMD/BMD", "Known maternal carrier status", "Clinical suspicion during pregnancy"] Measurement technique Confirm with laboratory Codes LOINC: 87762-1 ICD-10: G71.0 Clinical summary This test screens for common deletions and duplications within the 26 exons of the DMD gene, associated with Duchenne and Becker muscular dystrophies.
TEST-6346 DMGDH Gene (Dimethylglycine Dehydrogenase Deficiency) Genetic Test This genetic test identifies pathogenic variants in the DMGDH gene associated with dimethylglycine dehydrogenase deficiency.	Whole blood (EDTA), DNA FTA Card, or Extracted DNA (peripheral 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 DMGDH gene"] Parameters [] Preparation ["Fasting is not required", "Provide whole blood, DNA FTA card, or extracted DNA"] Indications ["Suspected dimethylglycine dehydrogenase deficiency", "Family history of the disorder", "Genetic counselling for at-risk relatives"] Measurement technique Confirm with laboratory Codes LOINC: 94558-4 ICD-10: E72.8, E72.9 Clinical summary This genetic test identifies pathogenic variants in the DMGDH gene associated with dimethylglycine dehydrogenase deficiency.
TEST-5028 DMP1 Gene Autosomal Recessive Hypophosphatemic Rickets Type 1 (ARHR1) Genetic Test This test evaluates the DMP1 gene for mutations associated with Autosomal Recessive Hypophosphatemic Rickets Type 1 (ARHR1).	Whole Blood (EDTA) or 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 ["DMP1 gene sequence", "Pathogenic variants in DMP1"] Parameters [] Preparation ["Pre-test genetic counselling session recommended", "Inform lab about recent blood transfusions"] Indications ["Suspected Autosomal Recessive Hypophosphatemic Rickets Type 1 (ARHR1)", "Family history of ARHR1", "Evaluation of hypophosphatemia with skeletal abnormalities"] Measurement technique Confirm with laboratory Codes LOINC: 79692-0 ICD-10: E83.31, Z13.79, Z82.79 Clinical summary This test evaluates the DMP1 gene for mutations associated with Autosomal Recessive Hypophosphatemic Rickets Type 1 (ARHR1).

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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