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

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450.00–30,000.00 AED

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Biochemistry test prices

Showing 46–60 of 1,113 matching tests.

Biochemistry diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-3609 ADAMTSL4 Gene Ectopia Lentis et Pupillae Genetic Test This test detects pathogenic variants in the ADAMTSL4 gene associated with ectopia lentis et pupillae.	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 ADAMTSL4 gene", "Full gene sequencing (exons, flanking introns, deep intronic variants)"] Parameters [] Preparation ["No fasting required", "Provide completed clinical history form", "Provide pedigree chart"] Indications ["Diagnosis of ectopia lentis et pupillae", "Differentiation from Marfan syndrome and homocystinuria", "Carrier screening", "Familial risk assessment", "Pre-surgical planning"] Measurement technique Confirm with laboratory Codes LOINC: 51234-5 ICD-10: Q12.1, H27.1 Clinical summary This test detects pathogenic variants in the ADAMTSL4 gene associated with ectopia lentis et pupillae.
TEST-3605 ADAR Gene Dyschromatosis Symmetrica Hereditaria Genetic Test This test identifies pathogenic variants in the ADAR gene associated with Dyschromatosis Symmetrica Hereditaria (DSH).	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 ADAR gene", "Full coding region and splice sites"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medications without consulting your physician"] Indications ["Confirmation of clinical diagnosis of DSH", "Family screening for DSH", "Genetic counselling"] Measurement technique Confirm with laboratory Codes LOINC: 43401-2 ICD-10: Q82.8, Z13.79, Z14.8 Clinical summary This test identifies pathogenic variants in the ADAR gene associated with Dyschromatosis Symmetrica Hereditaria (DSH).
TEST-4174 ADCY5 Gene Dyskinesia, Familial, with Facial Myokymia Genetic Test This genetic test identifies pathogenic variants in the ADCY5 gene associated with familial dyskinesia with facial myokymia.	Peripheral whole blood (EDTA tube) or saliva	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 ADCY5 gene"] Parameters [] Preparation ["Provide detailed clinical history", "Attend mandatory genetic counselling session"] Indications ["Suspected familial dyskinesia with facial myokymia", "Differential diagnosis of movement disorders"] Measurement technique Confirm with laboratory Codes LOINC: 83429-6 ICD-10: G25.89 Clinical summary This genetic test identifies pathogenic variants in the ADCY5 gene associated with familial dyskinesia with facial myokymia.
TEST-2732 ADK Gene Hypermethioninemia due to Adenosine Kinase Deficiency Genetic Test This genetic test evaluates the adenosine kinase (ADK) gene for pathogenic variants associated with hypermethioninemia.	Peripheral whole blood	3-4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Adenosine Kinase (ADK) gene sequence", "Pathogenic variants (SNVs, indels)"] Parameters [] Preparation ["No special preparation needed beyond routine hydration", "Complimentary genetic counselling session provided"] Indications ["Suspected Adenosine Kinase Deficiency", "Hypermethioninemia", "Family history of the disorder", "Carrier screening"] Measurement technique Confirm with laboratory Codes LOINC: 101404-3 ICD-10: E72.11 Clinical summary This genetic test evaluates the adenosine kinase (ADK) gene for pathogenic variants associated with hypermethioninemia.
TEST-5967 ADSL Gene Adenylosuccinase Deficiency Test This test evaluates the ADSL gene for pathogenic variants associated with Adenylosuccinase Deficiency, a rare inherited metabolic disorder.	Whole Blood (Peripheral)	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 ADSL gene"] Parameters [] Preparation [] Indications ["Suspected Adenylosuccinase Deficiency", "Family history of the disorder", "Neurological impairment of unknown origin"] Measurement technique Confirm with laboratory Codes LOINC: 94722-6 ICD-10: E79.8 Clinical summary This test evaluates the ADSL gene for pathogenic variants associated with Adenylosuccinase Deficiency, a rare inherited metabolic disorder.
TEST-1745 Advanced Inborn Errors of Metabolism (IEM) Extended Panel Test This test evaluates for a wide range of inborn errors of metabolism by quantifying specific amino acids, acylcarnitines, and organic acids in blood and urine.	Blood (Dried Blood Spot, Serum, Plasma) and Random Urine	3 Business Days	1,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Amino acids", "Acylcarnitines", "Organic acids", "Purines/pyrimidines"] Parameters [{"name": "Amino Acids", "reference_range": null}, {"name": "Acylcarnitines", "reference_range": null}, {"name": "Organic Acids", "reference_range": null}, {"name": "Purines/pyrimidines", "reference_range": null}] Preparation ["Fasting period of 4-6 hours as tolerated", "Avoid administering emergency medications before collection", "Provide complete documentation of dietary formulas, supplements, and drug history"] Indications ["Neonatal screening follow-up", "Unexplained developmental delay", "Adult-onset metabolic crisis", "Suspected inherited enzyme deficiency", "Differential diagnosis of metabolic disorders"] Measurement technique Confirm with laboratory Codes LOINC: 49289-7 ICD-10: E70.0, E71.1, Z13.228 Clinical summary This test evaluates for a wide range of inborn errors of metabolism by quantifying specific amino acids, acylcarnitines, and organic acids in blood and urine.
TEST-6123 AGA Gene Aspartylglucosaminuria Genetic Test This test performs full-coding-region sequencing of the AGA gene to detect pathogenic point mutations, small insertions or deletions, and copy-number variants associated with aspar...	Peripheral Whole Blood (EDTA), Extracted DNA, or FTA Blood Spot	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["AGA gene sequence", "Pathogenic variants (point mutations, insertions, deletions, copy-number variants)"] Parameters [] Preparation ["Complete pre-test genetic counseling session", "Provide a three-generation family pedigree"] Indications ["Diagnosis of aspartylglucosaminuria", "Carrier screening", "Prenatal testing"] Measurement technique Confirm with laboratory Codes LOINC: 94227-4 ICD-10: E77.1 Clinical summary This test performs full-coding-region sequencing of the AGA gene to detect pathogenic point mutations, small insertions or deletions, and copy-number variants associated with aspartylglucosaminuria.
TEST-3524 AGK Gene Cataract, Autosomal Recessive Type 38 Genetic Test This genetic test detects mutations in the AGK gene associated with congenital cataract and mitochondrial dysfunction.	Whole Blood (Peripheral)	3 – 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Mutations in the AGK gene"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist about anticoagulant therapy"] Indications ["Suspected autosomal recessive cataract type 38", "Family history of AGK-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 91727-1 ICD-10: Q12.0 Clinical summary This genetic test detects mutations in the AGK gene associated with congenital cataract and mitochondrial dysfunction.
TEST-3523 AGTR1 Gene Renal Tubular Dysgenesis Genetic Test This test identifies pathogenic mutations in the AGTR1 gene associated with autosomal recessive renal tubular dysgenesis.	Peripheral Whole Blood (EDTA) 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 AGTR1 gene", "Single nucleotide variants", "Small insertions/deletions", "Splice-site alterations"] Parameters [] Preparation [] Indications ["Diagnosis of suspected autosomal recessive renal tubular dysgenesis", "Family risk assessment", "Informed clinical management", "Carrier screening", "Family planning"] Measurement technique Confirm with laboratory Codes LOINC: 90507-6 ICD-10: Q61.4 Clinical summary This test identifies pathogenic mutations in the AGTR1 gene associated with autosomal recessive renal tubular dysgenesis.
TEST-5050 AGTR2 Gene Intellectual Disability (X-linked, MRX88) Genetic Test This genetic test analyzes the AGTR2 gene to detect mutations causing X-linked intellectual disability (MRX88). It identifies single-nucleotide variants, small insertions/deletions...	Peripheral Whole Blood – EDTA (2 mL)	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 AGTR2 gene", "Single-nucleotide variants", "Small insertions/deletions", "Splice-site mutations"] Parameters [] Preparation ["Genetic counseling session is mandatory before sample collection."] Indications ["Individuals with unexplained developmental delay", "Suspected X-linked intellectual disability (MRX88)", "Family history suggestive of X-linked inheritance"] Measurement technique Confirm with laboratory Codes LOINC: 82203-0 ICD-10: F78 Clinical summary This genetic test analyzes the AGTR2 gene to detect mutations causing X-linked intellectual disability (MRX88). It identifies single-nucleotide variants, small insertions/deletions, and splice-site mutations.
TEST-4674 AHI1 Gene (Joubert Syndrome Type 3) Genetic Test This genetic test evaluates the AHI1 gene for variants associated with Joubert syndrome type 3.	Whole Blood (EDTA)	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["AHI1 gene sequence", "Copy Number Variations (CNVs) in AHI1"] Parameters [] Preparation ["No fasting required", "Provide detailed clinical history", "Attend mandatory pre-genetic counselling session", "Bring previous MRI reports, neurology notes, and a list of current medications"] Indications ["Suspected Joubert syndrome type 3", "Family history of Joubert syndrome type 3", "Developmental delay with characteristic neuroimaging findings"] Measurement technique Confirm with laboratory Codes LOINC: 94425-5 ICD-10: Q04.3 Clinical summary This genetic test evaluates the AHI1 gene for variants associated with Joubert syndrome type 3.
TEST-5186 AKAP1 Gene Mitochondrial Disorders Genetic Test This test identifies pathogenic variants in the AKAP1 gene associated with mitochondrial encephalopathies.	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 AKAP1 gene", "Single-nucleotide variants", "Small insertions and deletions"] Parameters [] Preparation ["Inform the geneticist about all current medications and supplements.", "Do not discontinue any prescribed therapy without consulting your physician."] Indications ["Suspected mitochondrial encephalopathy", "Family history of AKAP1-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 82939-8 ICD-10: G71.3, G31.89, Z13.79 Clinical summary This test identifies pathogenic variants in the AKAP1 gene associated with mitochondrial encephalopathies.
TEST-6029 AKR1D1 Gene Bile Acid Synthesis Defect Type 2 Congenital Genetic Test This genetic test identifies disease-causing variants in the AKR1D1 gene, confirming a diagnosis of congenital bile acid synthesis defect type 2.	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 AKR1D1 gene", "Presence/absence of mutations affecting bile acid synthesis"] Parameters [] Preparation ["No fasting required", "Genetic counseling and informed consent required prior to collection"] Indications ["Infants with suspected bile acid synthesis defect type 2", "Neonatal cholestasis of unknown origin", "Family history of AKR1D1-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 79765-3 ICD-10: E78.7, Z15.89, K76.8 Clinical summary This genetic test identifies disease-causing variants in the AKR1D1 gene, confirming a diagnosis of congenital bile acid synthesis defect type 2.
TEST-142 Albumin and IgG Cerebrospinal Fluid (CSF) Test This diagnostic test evaluates the integrity of the blood-brain barrier and the production of immunoglobulins within the central nervous system.	Cerebrospinal Fluid (CSF)	Next day (sample by 4 PM Mon–Sat)	700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Blood–brain barrier integrity", "Intrathecal immunoglobulin synthesis"] Parameters [{"name": "Albumin", "reference_range": "0.5 mg/dL (linear detection)"}, {"name": "IgG", "reference_range": null}] Preparation [] Indications ["Differential diagnosis of multiple sclerosis", "Diagnosis of neuromyelitis optica spectrum disorders", "Evaluation of infectious neuropathies"] Measurement technique Confirm with laboratory Codes LOINC: ['2460-0', '2461-8'] ICD-10: ['G35', 'G36.0', 'G04.0'] Clinical summary This diagnostic test evaluates the integrity of the blood-brain barrier and the production of immunoglobulins within the central nervous system.
TEST-144 Alcaptonuria Urine Qualitative Test This test qualitatively detects homogentisic acid in urine, serving as a screening tool for the metabolic disorder alkaptonuria.	Urine (midstream, light-protected)	Same day (within 24 hours)	700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Homogentisic acid in urine"] Parameters [] Preparation ["Collect a freshly voided midstream urine specimen", "Wrap sample in aluminium foil", "Refrigerate sample immediately"] Indications ["Screening for alkaptonuria", "Investigation of dark urine", "Evaluation of suspected metabolic disorders"] Measurement technique Confirm with laboratory Codes LOINC: 2751-9 ICD-10: E70.2 Clinical summary This test qualitatively detects homogentisic acid in urine, serving as a screening tool for the metabolic disorder alkaptonuria.

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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