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

Confirm test-specific instructions with your clinician or laboratory.

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Biochemistry test prices

Showing 946–960 of 1,113 matching tests.

Biochemistry diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-5034 SLCO2A1 Gene Hypertrophic Osteoarthropathy Type 2 Genetic Test This genetic test identifies pathogenic variants in the SLCO2A1 gene associated with primary hypertrophic osteoarthropathy type 2.	Peripheral whole blood, FTA card, or pre-extracted DNA	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SLCO2A1 gene sequence", "Pathogenic variants (SNVs, indels, CNVs)"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication"] Indications ["Suspected primary hypertrophic osteoarthropathy type 2", "Family history of PHOAR2", "Differential diagnosis of clubbing and bone pain"] Measurement technique Confirm with laboratory Codes LOINC: 76002-6 ICD-10: M89.40 Clinical summary This genetic test identifies pathogenic variants in the SLCO2A1 gene associated with primary hypertrophic osteoarthropathy type 2.
TEST-227 SMA 26 Comprehensive Metabolic Panel Test This diagnostic test evaluates 26 key biochemical markers related to metabolic function, including glucose, electrolytes, liver enzymes, and kidney function.	Serum or Plasma (venous blood)	Same-day reporting (results before 10 PM)	450.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Glucose", "Renal function (e.g., Urea, Creatinine)", "Hepatic function (e.g., AST, ALT, Bilirubin)", "Electrolytes (e.g., Sodium, Potassium, Calcium)", "Protein profiles (e.g., Albumin, Total Protein)", "Uric Acid"] Parameters [{"name": "Glucose", "reference_range": null}, {"name": "Urea", "reference_range": null}, {"name": "Creatinine", "reference_range": null}, {"name": "Albumin", "reference_range": null}, {"name": "Total Protein", "reference_range": null}, {"name": "Calcium", "reference_range": null}, {"name": "Uric Acid", "reference_range": null}, {"name": "Bilirubin", "reference_range": null}, {"name": "AST", "reference_range": null}, {"name": "ALT", "reference_range": null}, {"name": "Sodium", "reference_range": null}, {"name": "Potassium", "reference_range": null}, {"name": "Chloride", "reference_range": null}, {"name": "CO2", "reference_range": null}] Preparation ["Minimum 12-hour overnight fast is mandatory.", "Water is permitted, but avoid coffee, gum, or smoking.", "Inform the lab about any medications you are taking."] Indications ["Routine health screening", "Monitoring chronic diseases (e.g., diabetes, kidney disease)", "Evaluation of metabolic disorders", "Pre-operative assessment"] Measurement technique Confirm with laboratory Codes LOINC: 24320-4 ICD-10: Z13.9 Clinical summary This diagnostic test evaluates 26 key biochemical markers related to metabolic function, including glucose, electrolytes, liver enzymes, and kidney function.
TEST-4819 SMAD3 Gene (Loeys‑Dietz Syndrome Type 1C) Genetic Test This genetic test identifies pathogenic variants in the SMAD3 gene associated with Loeys‑Dietz syndrome type 1C.	Whole Blood, Extracted DNA, 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 SMAD3 gene"] Parameters [] Preparation ["Complete clinical history form", "Genetic counseling session recommended"] Indications ["Suspected Loeys‑Dietz syndrome type 1C", "Family history of Loeys‑Dietz syndrome", "Confirmation of clinical diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q87.89 Clinical summary This genetic test identifies pathogenic variants in the SMAD3 gene associated with Loeys‑Dietz syndrome type 1C.
TEST-5297 SMC3 Gene (Cornelia de Lange Syndrome Type 3) Genetic Test This diagnostic test evaluates the SMC3 gene for pathogenic variants associated with Cornelia de Lange syndrome type 3.	Peripheral whole blood (EDTA) or 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 SMC3 gene", "Single nucleotide variants (SNVs)", "Copy number variations (CNVs)"] Parameters [] Preparation ["No specific fasting required", "Inform physician about current medications"] Indications ["Clinical signs suggestive of Cornelia de Lange syndrome type 3", "Need for definitive molecular diagnosis for management", "Family planning considerations"] Measurement technique Confirm with laboratory Codes LOINC: 60567-5 ICD-10: Q87.1 Clinical summary This diagnostic test evaluates the SMC3 gene for pathogenic variants associated with Cornelia de Lange syndrome type 3.
TEST-5520 SNCA Gene (PARK4) Parkinson Genetic Test This test evaluates the SNCA gene for pathogenic variants associated with autosomal dominant Parkinson's disease.	Peripheral whole blood, Extracted 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 SNCA gene coding region"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Individuals with clinical features suggestive of autosomal dominant Parkinson's disease", "Family members of individuals with known SNCA pathogenic variants"] Measurement technique Confirm with laboratory Codes LOINC: 80560-6 ICD-10: G20 Clinical summary This test evaluates the SNCA gene for pathogenic variants associated with autosomal dominant Parkinson's disease.
TEST-4993 SNRPE Gene Hypotrichosis Type 11 Genetic Test This test identifies pathogenic variants within the SNRPE gene associated with hereditary hypotrichosis type 11 using Next Generation Sequencing.	Whole Blood, 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 variants in the SNRPE gene", "Single nucleotide variants", "Small insertions and deletions", "Copy number variations"] Parameters [] Preparation ["Pre-test genetic counseling session recommended", "Construct a three-generation pedigree", "No fasting or special dietary preparation required", "Bring available medical records and family photographs"] Indications ["Family history of hypotrichosis type 11", "Clinical suspicion of hypotrichosis type 11", "Confirmation of genetic etiology before therapy"] Measurement technique Confirm with laboratory Codes LOINC: 94247-3 ICD-10: Q84.0 Clinical summary This test identifies pathogenic variants within the SNRPE gene associated with hereditary hypotrichosis type 11 using Next Generation Sequencing.
TEST-3392 SOHLH1 Gene Oogenesis Dysfunction Genetic Test This genetic test analyzes the SOHLH1 gene for variants associated with oogenesis dysfunction, primary ovarian insufficiency, and infertility.	Peripheral whole blood	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SOHLH1 gene variants", "Pathogenic mutations", "Novel variants"] Parameters [] Preparation [] Indications ["Primary ovarian insufficiency", "Unexplained infertility"] Measurement technique Confirm with laboratory Codes LOINC: 94138-2 ICD-10: E28.3, N97.0 Clinical summary This genetic test analyzes the SOHLH1 gene for variants associated with oogenesis dysfunction, primary ovarian insufficiency, and infertility.
TEST-2363 SOST Gene Sclerosteosis Type 1 Genetic Test This genetic test evaluates the SOST gene for pathogenic variants associated with Sclerosteosis type 1.	Whole Blood (EDTA) 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 SOST gene"] Parameters [] Preparation ["No specific fasting required", "Inform the phlebotomist about any medications"] Indications ["Suspected Sclerosteosis type 1 based on clinical or radiological findings", "Family history of Sclerosteosis type 1", "Genetic counselling for affected families"] Measurement technique Confirm with laboratory Codes LOINC: 33811-0 ICD-10: Q78.8 Clinical summary This genetic test evaluates the SOST gene for pathogenic variants associated with Sclerosteosis type 1.
TEST-5088 SOX3 Gene Genetic Test This test identifies pathogenic variants in the SOX3 gene associated with X-linked intellectual disability and isolated growth hormone deficiency.	Peripheral whole blood (EDTA) or dried blood spot (FTA card)	21–28 calendar days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the SOX3 gene", "Copy Number Variations (CNVs) in SOX3"] Parameters [] Preparation ["No fasting required", "Continue all prescribed medications unless advised otherwise by a physician"] Indications ["Individuals with clinical features suggestive of X-linked intellectual disability and isolated growth hormone deficiency", "Family history of SOX3-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 81315-0 ICD-10: E23.0 Clinical summary This test identifies pathogenic variants in the SOX3 gene associated with X-linked intellectual disability and isolated growth hormone deficiency.
TEST-3558 SOX3 Gene Panhypopituitarism, X-Linked Genetic Test This test identifies pathogenic sequence variants, deletions, and duplications in the SOX3 gene associated with X-linked panhypopituitarism.	Peripheral whole blood (EDTA tube), 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 SOX3 gene", "Copy number variants (deletions/duplications) in the SOX3 gene"] Parameters [] Preparation ["No fasting required", "No need to stop medications"] Indications ["Clinical suspicion of X-linked panhypopituitarism", "Family history suggestive of X-linked inheritance pattern", "Carrier screening in females"] Measurement technique Confirm with laboratory Codes LOINC: 81464-6 ICD-10: E23.0 Clinical summary This test identifies pathogenic sequence variants, deletions, and duplications in the SOX3 gene associated with X-linked panhypopituitarism.
TEST-4708 SP7 Gene Osteogenesis Imperfecta Type 12 Genetic Test This test detects pathogenic variants in the SP7 gene to diagnose autosomal recessive osteogenesis imperfecta type XII (OI-XII).	Whole blood (EDTA) 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 SP7 gene", "Copy number changes in the SP7 gene"] Parameters [] Preparation [] Indications ["Clinical and radiological findings suggesting OI type XII", "Familial genetic counseling for OI"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Q78.0 Clinical summary This test detects pathogenic variants in the SP7 gene to diagnose autosomal recessive osteogenesis imperfecta type XII (OI-XII).
TEST-5735 SPART (SPG20) Gene Genetic Test This test detects pathogenic variants in the SPG20 gene associated with hereditary spastic paraplegia (Troyer syndrome).	Whole blood (EDTA), dried blood spot (FTA card), or extracted DNA	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 SPG20 gene", "Single Nucleotide Variants (SNVs)", "Insertions/Deletions (indels)", "Copy Number Variations (CNVs)"] Parameters [] Preparation ["No fasting required", "No medication adjustments needed unless directed by physician"] Indications ["Suspected hereditary spastic paraplegia (Troyer syndrome)", "Progressive lower limb spasticity", "Family history of spastic paraplegia"] Measurement technique Confirm with laboratory Codes LOINC: 48817-2 ICD-10: G11.4 Clinical summary This test detects pathogenic variants in the SPG20 gene associated with hereditary spastic paraplegia (Troyer syndrome).
TEST-5758 SPAST Gene (SPG4) Next-Generation Sequencing (NGS) Genetic Test This test evaluates the SPAST gene for pathogenic mutations associated with hereditary spastic paraplegia type 4 (HSP-SPG4).	Peripheral whole blood (EDTA), extracted DNA, or FTA card sample	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 SPAST gene", "Single nucleotide variants", "Indels", "Copy number changes"] Parameters [] Preparation [] Indications ["Suspected hereditary spastic paraplegia (HSP)", "Family history of HSP", "Differentiation from other neurological disorders"] Measurement technique Confirm with laboratory Codes LOINC: 95803-7 ICD-10: G11.4 Clinical summary This test evaluates the SPAST gene for pathogenic mutations associated with hereditary spastic paraplegia type 4 (HSP-SPG4).
TEST-3150 Sphingolipidosis Panel 1 Test This diagnostic test evaluates lysosomal enzyme activity in whole blood to screen for Gaucher, Fabry, and Niemann-Pick diseases.	Whole Blood (peripheral venous)	4 working days (sample cut-off 4 pm daily)	1,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Lysosomal enzyme activity (glucocerebrosidase, alpha-galactosidase, sphingomyelinase)", "Sphingolipid metabolism"] Parameters [{"name": "Glucocerebrosidase Activity", "reference_range": null}, {"name": "Alpha-galactosidase Activity", "reference_range": null}, {"name": "Sphingomyelinase Activity", "reference_range": null}] Preparation ["No specific fasting required.", "No medication or diet restrictions unless advised by a physician."] Indications ["Screening for Gaucher disease", "Screening for Fabry disease", "Screening for Niemann-Pick diseases", "Evaluation of suspected lysosomal storage disorders in neonates and children"] Measurement technique Confirm with laboratory Codes LOINC: 47828-9 ICD-10: E75.2 Clinical summary This diagnostic test evaluates lysosomal enzyme activity in whole blood to screen for Gaucher, Fabry, and Niemann-Pick diseases.
TEST-3147 Sphingolipidosis Panel 2 Test This diagnostic test evaluates lysosomal enzyme activities in whole blood to identify specific sphingolipid storage disorders.	Whole blood	4 working days	900.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Lysosomal enzyme activities (Glucocerebrosidase, Sphingomyelinase, Alpha-galactosidase A)", "Biochemical markers for Gaucher disease, Niemann-Pick types A/B, Fabry disease"] Parameters [{"name": "Glucocerebrosidase", "reference_range": "nanomole/hour/mg protein (Specific range provided in lab report)"}, {"name": "Sphingomyelinase", "reference_range": "nanomole/hour/mg protein (Specific range provided in lab report)"}, {"name": "Alpha-galactosidase A", "reference_range": "nanomole/hour/mg protein (Specific range provided in lab report)"}] Preparation ["No fasting required.", "Inform physician about all current medications, especially enzyme replacement therapy or substrate reduction therapy."] Indications ["Suspicion of Gaucher disease", "Suspicion of Niemann-Pick types A/B", "Suspicion of Fabry disease", "Evaluation of unexplained neurological regression"] Measurement technique Confirm with laboratory Codes LOINC: 21046-5 ICD-10: E75.2 Clinical summary This diagnostic test evaluates lysosomal enzyme activities in whole blood to identify specific sphingolipid storage disorders.

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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