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.

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1,113

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450.00–30,000.00 AED

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Biochemistry test prices

Showing 361–375 of 1,113 matching tests.

Biochemistry diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-5084 EXT1 Gene Exostoses, Multiple, Type 1 Test This test evaluates the EXT1 gene for pathogenic variants associated with Hereditary Multiple Exostoses (Type 1). It identifies genetic mutations linked to the development of multi...	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 variants in the EXT1 gene", "Copy Number Variations (CNV) in EXT1"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication"] Indications ["Confirmation of clinical diagnosis of Hereditary Multiple Exostoses (Type 1)", "Genetic counselling for families with HME", "Guiding surveillance strategies"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q78.6 Clinical summary This test evaluates the EXT1 gene for pathogenic variants associated with Hereditary Multiple Exostoses (Type 1). It identifies genetic mutations linked to the development of multiple benign bone tumors (osteochondromas).
TEST-2681 Extended Newborn Screening Panel Test This diagnostic test evaluates a newborn's blood sample for over 50 inborn errors of metabolism, endocrine disorders, and hemoglobinopathies.	Dried Blood Spot (heel prick)	Next day (samples accepted Mon/Wed/Fri by 9 AM)	1,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Metabolic disorders", "Endocrine disorders", "Hemoglobinopathies"] Parameters [{"name": "Inborn Errors of Metabolism", "reference_range": "Detected via LC-MS/MS and immunoassays"}, {"name": "Endocrine Disorders", "reference_range": "Detected via LC-MS/MS and immunoassays"}, {"name": "Hemoglobinopathies", "reference_range": "Detected via LC-MS/MS and immunoassays"}] Preparation ["No specific fasting required", "Inform lab if baby is on TPN or antibiotics"] Indications ["Newborn screening", "Detection of inborn errors of metabolism", "Detection of endocrine disorders", "Detection of hemoglobinopathies"] Measurement technique Confirm with laboratory Codes LOINC: 73793-4 ICD-10: Z13.2 Clinical summary This diagnostic test evaluates a newborn's blood sample for over 50 inborn errors of metabolism, endocrine disorders, and hemoglobinopathies.
TEST-5795 EYA1 Gene Branchiootic Syndrome Type 1 Genetic Test This test identifies pathogenic variants in the EYA1 gene to diagnose Branchiootic Syndrome Type 1.	Whole Blood (EDTA, 3–5 mL) or Extracted DNA (≥1 µg, A260/A280: 1.8–2.0)	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 EYA1 gene", "Full coding region + splice sites"] Parameters [{"name": "EYA1 Gene Analysis", "reference_range": "No pathogenic variants detected"}] Preparation ["Discontinue high-dose biotin (>5 mg/day) supplementation 72 hours prior to blood draw."] Indications ["Congenital ear anomalies", "Branchial cleft fistulae", "Preauricular tags", "Guiding otologic surgical planning", "Audiological rehabilitation", "Familial genetic risk stratification"] Measurement technique Confirm with laboratory Codes LOINC: 94219-4 ICD-10: Q87.0 Clinical summary This test identifies pathogenic variants in the EYA1 gene to diagnose Branchiootic Syndrome Type 1.
TEST-3835 F12 Gene (Factor XII Deficiency) Genetic Test This genetic test evaluates the F12 gene for mutations associated with Factor XII deficiency and Hereditary Angioedema type III.	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 F12 gene", "Carrier status for F12 gene mutations", "Risk for Hereditary Angioedema type III (HAE-FXII)"] Parameters [{"name": "Analytical Sensitivity", "reference_range": ">99.9%"}, {"name": "Analytical Specificity", "reference_range": ">99.9%"}] Preparation ["No specific fasting required", "Consult your doctor regarding medication adjustments"] Indications ["Diagnosis of hereditary Factor XII deficiency", "Diagnosis of Hereditary Angioedema type III (HAE-FXII)", "Identification of carriers for F12 gene mutations", "Family screening for F12 gene mutations"] Measurement technique Confirm with laboratory Codes LOINC: 21636-3 ICD-10: D68.2, E88.0 Clinical summary This genetic test evaluates the F12 gene for mutations associated with Factor XII deficiency and Hereditary Angioedema type III.
TEST-4050 F2 (Prothrombin) Gene Mutation Analysis (NGS) Test This test detects the G20210A mutation in the F2 (Prothrombin) gene, a common inherited risk factor for venous thromboembolism.	Peripheral whole blood (3–5 mL in EDTA tube) 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 ["G20210A mutation in the F2 gene", "Inherited thrombophilia risk"] Parameters [{"name": "G20210A Mutation Status", "reference_range": "Negative/Positive"}] Preparation ["No special preparation is required"] Indications ["Evaluation of inherited thrombophilia", "Risk assessment for VTE", "Pre-surgical assessment in high-risk individuals"] Measurement technique Confirm with laboratory Codes LOINC: 59228-8 ICD-10: D68.51 Clinical summary This test detects the G20210A mutation in the F2 (Prothrombin) gene, a common inherited risk factor for venous thromboembolism.
TEST-6261 F5 Gene Factor V Deficiency Genetic Test This test evaluates the F5 gene for pathogenic variants associated with Factor V deficiency.	Peripheral Whole Blood or DNA Extract	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["F5 gene variants", "Pathogenic mutations"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medications without consulting your physician"] Indications ["Suspected Factor V deficiency", "Personal or family history of bleeding disorders", "Need for definitive molecular diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 55383-1 ICD-10: D68.51 Clinical summary This test evaluates the F5 gene for pathogenic variants associated with Factor V deficiency.
TEST-1087 Fabry Disease Quantitative Blood Test This diagnostic test evaluates the activity level of the alpha-galactosidase A enzyme in whole blood.	Whole Blood	4 Business Days (Sample received by 4 pm daily)	600.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Alpha-galactosidase A enzyme activity"] Parameters [{"name": "Alpha-Galactosidase A Activity", "reference_range": "null"}] Preparation ["No specific fasting required.", "Inform phlebotomist about any medications, especially anticoagulants."] Indications ["Screening for Fabry disease", "Monitoring treatment response in Fabry disease patients", "Investigation of symptoms suggestive of lysosomal storage disorders"] Measurement technique Confirm with laboratory Codes LOINC: 33330-0 ICD-10: E75.21 Clinical summary This diagnostic test evaluates the activity level of the alpha-galactosidase A enzyme in whole blood.
TEST-3879 Factor XI Deficiency (F11) Gene Sequencing Test (NGS) This test evaluates the F11 gene for pathogenic variants associated with hereditary Factor XI deficiency.	Blood (EDTA), Extracted DNA, or FTA Card Blood Spot	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["F11 gene sequence", "Pathogenic variants in coding exons and splice junctions"] Parameters [] Preparation ["Pre-genetic counseling session is mandatory", "No fasting required", "Inform team if on anticoagulants"] Indications ["Suspected hereditary Factor XI deficiency", "Personal or family history suggestive of the disorder"] Measurement technique Confirm with laboratory Codes LOINC: 83142-5 ICD-10: D68.1 Clinical summary This test evaluates the F11 gene for pathogenic variants associated with hereditary Factor XI deficiency.
TEST-5826 FAH Gene Tyrosinemia Type 1 Genetic Test This test evaluates the FAH gene for pathogenic variants associated with Tyrosinemia Type 1.	Peripheral whole blood (3 ml EDTA) or buccal swab	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["FAH gene sequence", "Pathogenic variants (SNVs, indels, splice-site variants)"] Parameters [] Preparation ["No fasting required", "Pre-test genetic counselling is mandatory"] Indications ["Suspected Tyrosinemia Type 1", "Family history of Tyrosinemia Type 1", "Screening in high-risk populations"] Measurement technique Confirm with laboratory Codes LOINC: 94851-1 ICD-10: E70.21 Clinical summary This test evaluates the FAH gene for pathogenic variants associated with Tyrosinemia Type 1.
TEST-5450 FAM20A Gene Amelogenesis Imperfecta Type 1G Genetic Test This genetic test evaluates the FAM20A gene for pathogenic variants associated with Amelogenesis Imperfecta Type IG.	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 ["FAM20A gene sequence variants", "Pathogenic mutations"] Parameters [] Preparation ["No fasting required", "No special dietary restrictions"] Indications ["Diagnosis of Amelogenesis Imperfecta Type IG", "Identification of FAM20A gene mutations", "Genetic counseling for affected families", "Reproductive planning"] Measurement technique Confirm with laboratory Codes LOINC: 96208-4 ICD-10: K00.5 Clinical summary This genetic test evaluates the FAM20A gene for pathogenic variants associated with Amelogenesis Imperfecta Type IG.
TEST-4612 FAM20C Gene Raine Syndrome Genetic Test This test identifies pathogenic variants in the FAM20C gene associated with Raine syndrome.	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 ["FAM20C gene sequence", "Single nucleotide variants", "Small insertions/deletions", "Copy number alterations"] Parameters [] Preparation [] Indications ["Clinical suspicion of Raine syndrome", "Documented family history of Raine syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 94762-2 ICD-10: Q78.8 Clinical summary This test identifies pathogenic variants in the FAM20C gene associated with Raine syndrome.
TEST-6274 Fanconi Anemia Type D2 (FANCD2) Gene Genetic Test This test identifies pathogenic variants within the FANCD2 gene associated with Fanconi anemia type D2.	Whole blood (EDTA), extracted DNA, or FTA card (dried blood spot)	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 FANCD2 gene", "Copy number variants (CNVs) in the FANCD2 gene"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication without consulting your doctor"] Indications ["Diagnosis of Fanconi anemia type D2", "Carrier screening", "Reproductive planning"] Measurement technique Confirm with laboratory Codes LOINC: 101516-4 ICD-10: D61.01, Z14.8, Z13.7 Clinical summary This test identifies pathogenic variants within the FANCD2 gene associated with Fanconi anemia type D2.
TEST-5243 FBLN5 Gene Cutis Laxa Type 1A Genetic Test This diagnostic test evaluates the FBLN5 gene for pathogenic variants associated with autosomal recessive cutis laxa type 1A.	Peripheral Whole Blood (EDTA), FTA Card, or Extracted Genomic DNA	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["FBLN5 gene sequence", "Pathogenic variants in FBLN5"] Parameters [] Preparation ["No fasting required", "No medication adjustments needed"] Indications ["Suspected cutis laxa type 1A", "Family history of cutis laxa type 1A", "Carrier screening for at-risk family members"] Measurement technique Confirm with laboratory Codes LOINC: 81254-5 ICD-10: Q82.8 Clinical summary This diagnostic test evaluates the FBLN5 gene for pathogenic variants associated with autosomal recessive cutis laxa type 1A.
TEST-2820 FBN1 Gene Geleophysic Dysplasia Type 2 Genetic Test This test identifies pathogenic variants in the FBN1 gene associated with Geleophysic Dysplasia Type 2.	Peripheral whole blood (EDTA), extracted DNA, or FTA card blood spot	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["FBN1 gene sequence", "FBN1 gene copy number variations (deletions/duplications)"] Parameters [] Preparation ["No specific fasting required", "No medication or diet restrictions"] Indications ["Suspected Geleophysic Dysplasia Type 2", "Family history of FBN1-related disorders", "Need for genetic confirmation for clinical management"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: Q87.1 Clinical summary This test identifies pathogenic variants in the FBN1 gene associated with Geleophysic Dysplasia Type 2.
TEST-6383 FBP1 Gene Fructose-1,6-Bisphosphatase Deficiency Genetic Test This genetic test identifies mutations in the FBP1 gene associated with fructose-1,6-bisphosphatase deficiency.	Peripheral Whole Blood 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 ["FBP1 gene mutations", "Single nucleotide variants", "Small deletions or duplications"] Parameters [] Preparation ["Genetic counselling session required", "Detailed family pedigree documentation", "Full clinical history recording"] Indications ["Suspected fructose-1,6-bisphosphatase deficiency", "Newborn screening follow-up", "Family history of the disorder"] Measurement technique Confirm with laboratory Codes LOINC: 94124-8 ICD-10: E74.04 Clinical summary This genetic test identifies mutations in the FBP1 gene associated with fructose-1,6-bisphosphatase 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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