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 16–30 of 1,113 matching tests.

Biochemistry diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4054 ABCA1 Gene Genetic Test for Coronary Artery Disease & Familial Hypercholesterolemia Susceptibility This test evaluates the ABCA1 gene for pathogenic variants linked to premature coronary artery disease and familial hypercholesterolemia.	Whole Blood / Peripheral Blood	3 – 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ABCA1 gene pathogenic variants", "Cholesterol efflux regulation", "HDL metabolism"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any relevant family history"] Indications ["Assessment of hereditary risk for CAD", "Evaluation for familial hypercholesterolemia", "Risk stratification in individuals with dyslipidemia"] Measurement technique Confirm with laboratory Codes LOINC: 92031-4 ICD-10: E78.0, I25.1 Clinical summary This test evaluates the ABCA1 gene for pathogenic variants linked to premature coronary artery disease and familial hypercholesterolemia.
TEST-3356 ABCB7 Gene Sideroblastic Anemia with Ataxia Genetic Test This test sequences the ABCB7 gene to detect pathogenic variants associated with X-linked sideroblastic anemia with ataxia.	Whole Blood (peripheral venous)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ABCB7 gene sequence", "Pathogenic variants in ABCB7"] Parameters [] Preparation ["No specific fasting required", "Avoid recent blood transfusion (within 2 weeks)"] Indications ["Suspected X-linked sideroblastic anemia with ataxia", "Family history of the condition", "Need for definitive molecular diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 87039-8 ICD-10: D64.0 Clinical summary This test sequences the ABCB7 gene to detect pathogenic variants associated with X-linked sideroblastic anemia with ataxia.
TEST-3887 ABCC2 Gene Dubin-Johnson Syndrome Genetic Test This genetic test evaluates the ABCC2 gene for mutations associated with Dubin-Johnson syndrome.	Peripheral Whole Blood	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Mutations in the ABCC2 gene", "Exons and flanking regions of the ABCC2 gene"] Parameters [{"name": "Method", "reference_range": "Next-Generation Sequencing (NGS)"}, {"name": "Detection Sensitivity", "reference_range": "99.9%"}, {"name": "Turnaround Time", "reference_range": "3–4 Weeks"}] Preparation ["No fasting required", "Continue prescribed medications"] Indications ["Diagnosis of Dubin-Johnson syndrome", "Family risk assessment", "Differentiation from other causes of hyperbilirubinemia"] Measurement technique Confirm with laboratory Codes LOINC: 69047-9 ICD-10: E80.6 Clinical summary This genetic test evaluates the ABCC2 gene for mutations associated with Dubin-Johnson syndrome.
TEST-4637 ABCC6 Gene Pseudoxanthoma Elasticum (Forme Fruste) Genetic Test This genetic test evaluates the ABCC6 gene for pathogenic variants associated with pseudoxanthoma elasticum (PXE) and its forme fruste presentation.	Peripheral Whole Blood	3–4 Weeks (Express: 14 Business Days)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the ABCC6 gene", "Single Nucleotide Variants (SNVs)", "Insertions/Deletions (Indels)", "Copy Number Variants (CNVs)"] Parameters [] Preparation ["No specific fasting required", "Inform lab of recent blood transfusions (wait 4 weeks)", "Inform lab of bleeding disorders"] Indications ["Suspicion of Pseudoxanthoma Elasticum (PXE)", "Family history of PXE", "Carrier screening", "Differential diagnosis of skin or vascular conditions"] Measurement technique Confirm with laboratory Codes LOINC: 99157-1 ICD-10: Q82.8 Clinical summary This genetic test evaluates the ABCC6 gene for pathogenic variants associated with pseudoxanthoma elasticum (PXE) and its forme fruste presentation.
TEST-4617 ABCC6 Gene Pseudoxanthoma Elasticum Genetic Test This genetic test analyzes the ABCC6 gene to detect pathogenic variants associated with pseudoxanthoma elasticum (PXE).	Whole Blood or DNA FTA Card	3 to 4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the ABCC6 gene", "Genetic predisposition to Pseudoxanthoma Elasticum"] Parameters [] Preparation ["No fasting required", "Inform phlebotomist of anticoagulant medications"] Indications ["Diagnosis of suspected Pseudoxanthoma Elasticum (PXE)", "Genetic counseling for families with PXE", "Clinical management of PXE patients"] Measurement technique Confirm with laboratory Codes LOINC: 20316-4 ICD-10: Q82.8 Clinical summary This genetic test analyzes the ABCC6 gene to detect pathogenic variants associated with pseudoxanthoma elasticum (PXE).
TEST-4041 ABCC6 Gene Sequencing for Generalized Arterial Calcification Type 2 (Infantile) Test This test identifies pathogenic variants within the ABCC6 gene, the primary cause of Generalized Arterial Calcification of Infancy (GACI) type 2.	Peripheral whole blood (EDTA tube)	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 ABCC6 gene", "Copy number variants in the ABCC6 gene"] Parameters [] Preparation [] Indications ["Diagnosis of GACI type 2", "Family planning for GACI type 2"] Measurement technique Confirm with laboratory Codes LOINC: 21615-9 ICD-10: E83.59 Clinical summary This test identifies pathogenic variants within the ABCC6 gene, the primary cause of Generalized Arterial Calcification of Infancy (GACI) type 2.
TEST-6126 ABCC8 Gene (Hypoglycemia of Infancy, Leucine-Sensitive) Next‑Generation Sequencing Genetic Test This test identifies pathogenic variants in the ABCC8 gene associated with congenital hyperinsulinism and leucine-sensitive hypoglycemia.	Peripheral Whole Blood (3–5 mL in EDTA tube)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ABCC8 gene sequence", "Pathogenic variants in coding exons and splice sites"] Parameters [] Preparation ["Genetic counselling session required prior to sample collection", "Detailed family pedigree required prior to sample collection"] Indications ["Diagnosis of congenital hyperinsulinism", "Identification of leucine-sensitive hypoglycemia", "Genetic counselling for families with affected individuals"] Measurement technique Confirm with laboratory Codes LOINC: 81198-4 ICD-10: E16.1 Clinical summary This test identifies pathogenic variants in the ABCC8 gene associated with congenital hyperinsulinism and leucine-sensitive hypoglycemia.
TEST-6241 ABCC8 Gene Hyperinsulinemic Hypoglycemia Type 1 Genetic Test This genetic test detects pathogenic variants in the ABCC8 gene associated with congenital hyperinsulinemic hypoglycemia type 1.	Whole Blood (1 mL) 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 ABCC8 gene", "Coding region analysis"] Parameters [] Preparation ["No fasting required", "No medication adjustment needed unless directed by doctor"] Indications ["Suspected congenital hyperinsulinemic hypoglycemia", "Need to differentiate diffuse from focal disease", "Guiding treatment planning for hyperinsulinism"] Measurement technique Confirm with laboratory Codes LOINC: 97920-5 ICD-10: E16.1, Z13.79, Z84.89 Clinical summary This genetic test detects pathogenic variants in the ABCC8 gene associated with congenital hyperinsulinemic hypoglycemia type 1.
TEST-4423 ABCC9 Gene Atrial Fibrillation Type 12 Genetic Test This test evaluates the ABCC9 gene for pathogenic variants associated with familial atrial fibrillation type 12.	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 ABCC9 gene", "Single nucleotide variants", "Small insertions or deletions"] Parameters [] Preparation ["Mandatory pre-test genetic counseling teleconsultation"] Indications ["Individuals with a strong family history of early-onset atrial fibrillation", "Patients with unexplained atrial fibrillation and a suggestive pedigree", "Individuals with atrial fibrillation and cardiomyopathy"] Measurement technique Confirm with laboratory Codes LOINC: 81269-7 ICD-10: I48.0, I48.1, I48.2, I48.3, I48.4, I48.91 Clinical summary This test evaluates the ABCC9 gene for pathogenic variants associated with familial atrial fibrillation type 12.
TEST-6036 ABCD4 Gene Methylmalonic Aciduria CblJ Type Genetic Test This test identifies pathogenic variants in the ABCD4 gene, confirming a diagnosis of methylmalonic aciduria, CblJ type.	5 mL EDTA Whole Blood	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ABCD4 gene sequence", "Pathogenic variants"] Parameters [] Preparation ["Complete pre-test genetic counselling session", "Avoid blood transfusion within 14 days prior to collection"] Indications ["Suspected methylmalonic aciduria, CblJ type", "Family cascade screening"] Measurement technique Confirm with laboratory Codes LOINC: 21656-9 ICD-10: E71.120 Clinical summary This test identifies pathogenic variants in the ABCD4 gene, confirming a diagnosis of methylmalonic aciduria, CblJ type.
TEST-4735 ACAD9 Gene Leigh Syndrome and Mitochondrial Encephalopathy Genetic Test This test identifies pathogenic variants in the ACAD9 gene associated with Leigh syndrome and mitochondrial encephalopathy.	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 ["ACAD9 gene sequence", "Copy Number Variations (CNVs) in ACAD9"] Parameters [] Preparation ["Provide a detailed three-generation family pedigree", "Complete clinical history during pre-test genetic counselling"] Indications ["Clinical suspicion of Leigh syndrome", "Clinical suspicion of mitochondrial encephalopathy", "Family history of mitochondrial disorders"] Measurement technique Confirm with laboratory Codes LOINC: 81315-5 ICD-10: G31.82, E88.49 Clinical summary This test identifies pathogenic variants in the ACAD9 gene associated with Leigh syndrome and mitochondrial encephalopathy.
TEST-6130 ACADL Gene LCAD Deficiency Genetic Test This test analyzes the ACADL gene for pathogenic variants associated with Long-Chain Acyl-CoA Dehydrogenase (LCAD) deficiency, an inherited metabolic disorder.	Peripheral Whole Blood (EDTA) or Dried Blood Spot (DBS)	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 ACADL gene", "Single Nucleotide Variants (SNVs)", "Insertions/Deletions (Indels)", "Copy Number Variations (CNVs)"] Parameters [] Preparation ["No specific fasting required for blood sample.", "Inform lab of any medications or dietary modifications."] Indications ["Clinical suspicion of LCAD deficiency", "Carrier testing", "Family screening", "Guiding dietary management"] Measurement technique Confirm with laboratory Codes LOINC: 21661-2 ICD-10: E71.39 Clinical summary This test analyzes the ACADL gene for pathogenic variants associated with Long-Chain Acyl-CoA Dehydrogenase (LCAD) deficiency, an inherited metabolic disorder.
TEST-5955 ACADM Gene (Medium-Chain Acyl-CoA Dehydrogenase Deficiency) Genetic Test This genetic test identifies pathogenic variants in the ACADM gene associated with Medium-Chain Acyl-CoA Dehydrogenase Deficiency (MCAD deficiency).	Peripheral Whole Blood (EDTA tube)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ACADM gene sequence", "Pathogenic variants"] Parameters [] Preparation ["No fasting required", "Provide complete family history", "Provide previous metabolic test results"] Indications ["Newborn screening abnormalities", "Unexplained hypoglycemia", "Family history of MCAD deficiency", "Sudden infant death"] Measurement technique Confirm with laboratory Codes LOINC: 82232-2 ICD-10: E71.31 Clinical summary This genetic test identifies pathogenic variants in the ACADM gene associated with Medium-Chain Acyl-CoA Dehydrogenase Deficiency (MCAD deficiency).
TEST-5911 ACADSB Gene 2‑Methylbutyrylglycinuria Genetic Test This genetic test evaluates the ACADSB gene for pathogenic variants associated with 2‑methylbutyrylglycinuria.	Peripheral Whole Blood (EDTA) or Saliva (Oragene)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ACADSB gene sequence", "Copy Number Variations (CNV) in ACADSB"] Parameters [] Preparation ["Do not discontinue prescribed medication", "Do not alter dietary supplements or metabolic formulas without physician consultation"] Indications ["Clinical suspicion of 2‑methylbutyrylglycinuria", "Carrier screening", "Family planning"] Measurement technique Confirm with laboratory Codes LOINC: 55230-4 ICD-10: E71.11 Clinical summary This genetic test evaluates the ACADSB gene for pathogenic variants associated with 2‑methylbutyrylglycinuria.
TEST-5963 ACADVL (Very Long-Chain Acyl-CoA Dehydrogenase) Deficiency Genetic Test This test evaluates the ACADVL gene for pathogenic variants associated with Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) deficiency.	Whole Blood (Peripheral)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ACADVL gene sequence", "Pathogenic variants in ACADVL gene"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication without doctor guidance"] Indications ["Suspected VLCAD deficiency", "Family history of VLCAD deficiency", "Carrier screening"] Measurement technique Confirm with laboratory Codes LOINC: 96538-9 ICD-10: E71.310 Clinical summary This test evaluates the ACADVL gene for pathogenic variants associated with Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) 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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