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

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Biochemistry test prices

Showing 871–885 of 1,113 matching tests.

Biochemistry diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4614 RYR1 Gene Sequencing for King-Denborough Syndrome Test This test evaluates the RYR1 gene for pathogenic variants associated with King-Denborough syndrome and malignant hyperthermia susceptibility.	Peripheral whole blood (preferred) or buccal swab	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 RYR1 gene", "Single Nucleotide Variants (SNVs)", "Insertions/Deletions (indels)", "Copy Number Changes"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication without consulting a doctor"] Indications ["Suspected King-Denborough syndrome", "Evaluation of malignant hyperthermia susceptibility", "Family screening for RYR1-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 82283-4 ICD-10: G71.2 Clinical summary This test evaluates the RYR1 gene for pathogenic variants associated with King-Denborough syndrome and malignant hyperthermia susceptibility.
TEST-3628 SALL4 Gene Analysis for Duane Retraction Syndrome (Genetic Test) This test identifies pathogenic variants in the SALL4 gene associated with Duane retraction syndrome and related disorders.	Peripheral Whole Blood (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 ["SALL4 gene sequence variants (SNVs, Indels)", "SALL4 gene copy number variations (CNVs)"] Parameters [] Preparation ["No fasting required", "Inform the team of any bleeding disorders or anticoagulant medication", "A mandatory pre-test genetic counselling session is required"] Indications ["Suspected Duane retraction syndrome (DRS)", "Suspected Okihiro syndrome (Duane-radial ray syndrome)", "Family history of DRS or related disorders", "Need for genetic counselling and reproductive planning"] Measurement technique Confirm with laboratory Codes LOINC: 21705-3 ICD-10: Z13.71, H50.813, Q87.0 Clinical summary This test identifies pathogenic variants in the SALL4 gene associated with Duane retraction syndrome and related disorders.
TEST-3634 SAMD9 Gene Mirage Syndrome Genetic Test This test analyzes the SAMD9 gene for pathogenic variants associated with Mirage syndrome using Next-Generation Sequencing.	Peripheral Blood (FTA card or venous draw)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Single nucleotide variants in SAMD9 gene", "Small indels in SAMD9 gene", "Copy number variations (CNV) in SAMD9 gene"] Parameters [] Preparation ["No specific fasting required", "Avoid recent blood transfusion ( Indications ["Suspected clinical diagnosis of Mirage syndrome", "Differentiation from other bone marrow failure syndromes"] Measurement technique Confirm with laboratory Codes LOINC: 93390-1 ICD-10: Q87.89, D46.9, Z15.89 Clinical summary This test analyzes the SAMD9 gene for pathogenic variants associated with Mirage syndrome using Next-Generation Sequencing.
TEST-3747 SAMHD1 Gene Aicardi-Goutières Syndrome Type 5 Genetic Test This genetic test detects pathogenic variants in the SAMHD1 gene to diagnose Aicardi-Goutières syndrome type 5.	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 ["Pathogenic variants in the SAMHD1 gene", "Single-nucleotide variants", "Small insertions/deletions", "Copy-number variations"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Suspected Aicardi-Goutières syndrome type 5", "Early-onset encephalopathy of unknown origin", "Family history of Aicardi-Goutières syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 92841-1 ICD-10: G31.82, Z13.71 Clinical summary This genetic test detects pathogenic variants in the SAMHD1 gene to diagnose Aicardi-Goutières syndrome type 5.
TEST-6000 SBDS Gene-Related Aplastic Anemia Genetic Test This test evaluates the SBDS gene for pathogenic variants associated with Shwachman-Diamond syndrome and constitutional aplastic anemia.	Peripheral blood, 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 ["SBDS gene coding region", "Copy Number Variations (CNV)"] Parameters [] Preparation ["Do not discontinue prescribed medication or supplements affecting blood counts without physician instruction."] Indications ["Suspected Shwachman-Diamond syndrome", "Constitutional aplastic anemia", "Family history of related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: D61.0 Clinical summary This test evaluates the SBDS gene for pathogenic variants associated with Shwachman-Diamond syndrome and constitutional aplastic anemia.
TEST-4437 SCN1A Gene Sequencing for GEFS+ Type 2 Test This test identifies pathogenic variants in the SCN1A gene associated with Generalized Epilepsy with Febrile Seizures Plus (GEFS+) Type 2.	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 variants in SCN1A gene", "Sodium channel dysfunction"] Parameters [] Preparation [] Indications ["Diagnosis of GEFS+ Type 2", "Guiding antiepileptic therapy", "Family planning"] Measurement technique Confirm with laboratory Codes LOINC: 48306-0 ICD-10: G40.3 Clinical summary This test identifies pathogenic variants in the SCN1A gene associated with Generalized Epilepsy with Febrile Seizures Plus (GEFS+) Type 2.
TEST-5405 SCN4A Gene NGS Test for Paramyotonia Congenita (von Eulenburg) This test sequences the entire SCN4A gene to detect mutations associated with paramyotonia congenita.	EDTA 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 ["SCN4A gene sequence", "Point mutations", "Small deletions/insertions", "Copy number variants"] Parameters [] Preparation ["No fasting required", "No medication stoppage required", "Mandatory pre-test genetic counselling"] Indications ["Suspected paramyotonia congenita", "Family history of myotonia", "Differential diagnosis of myotonic disorders"] Measurement technique Confirm with laboratory Codes LOINC: 81314-2 ICD-10: G71.1 Clinical summary This test sequences the entire SCN4A gene to detect mutations associated with paramyotonia congenita.
TEST-4089 SCN5A Gene (Ventricular Fibrillation, Familial Paroxysmal Type 1) Genetic Test This test analyzes the SCN5A gene for variants associated with inherited cardiac arrhythmias and sudden cardiac death risk.	Whole Blood (EDTA) or DNA (FTA Card)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SCN5A gene variants", "Pathogenic and likely pathogenic variants"] Parameters [] Preparation ["No fasting or special preparation is required."] Indications ["Evaluation of familial paroxysmal ventricular fibrillation type 1", "Risk stratification for sudden cardiac death", "Guidance for ICD placement", "Family cascade screening"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: I49.01 Clinical summary This test analyzes the SCN5A gene for variants associated with inherited cardiac arrhythmias and sudden cardiac death risk.
TEST-4464 SCN9A Gene Primary Erythromelalgia Genetic Test This test evaluates the SCN9A gene for mutations associated with primary erythromelalgia.	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 ["SCN9A gene sequence", "Pathogenic variants (SNVs, indels)"] Parameters [] Preparation [] Indications ["Suspected inherited erythromelalgia", "Differential diagnosis of neuropathic pain", "Familial risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 94026-8 ICD-10: I73.81 Clinical summary This test evaluates the SCN9A gene for mutations associated with primary erythromelalgia.
TEST-4169 SCN9A Gene Sequencing (NGS) for Dravet Syndrome Modifier Variants Test This test identifies genetic variants in the SCN9A gene that may modify the clinical presentation and treatment response in individuals with Dravet syndrome.	Whole Blood (EDTA), extracted DNA, or dried blood spot (FTA card)	3–4 weeks (expedited available)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SCN9A gene variants (missense, nonsense, splice-site, copy-number variants)", "Phenotypic modifiers influencing Dravet syndrome severity"] Parameters [] Preparation ["No fasting required", "No medication discontinuation unless advised by physician"] Indications ["Prognostic assessment in SCN1A-positive Dravet syndrome", "Guidance for personalized treatment strategies", "Understanding phenotypic variability in Dravet syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 94762-2 ICD-10: G40.3 Clinical summary This test identifies genetic variants in the SCN9A gene that may modify the clinical presentation and treatment response in individuals with Dravet syndrome.
TEST-6151 SCNN1A Gene Bronchiectasis with or without Elevated Sweat Chloride Type 2 Genetic Test This diagnostic test evaluates the SCNN1A gene for pathogenic variants associated with bronchiectasis and elevated sweat chloride levels.	Whole Blood (3–5 mL), 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 ["SCNN1A gene pathogenic variants", "Copy Number Variations (CNV) in SCNN1A"] Parameters [] Preparation ["No fasting required", "Continue regular medications unless advised otherwise by a doctor", "Genetic counselling must be completed prior to sampling"] Indications ["Diagnosis of genetic predisposition to bronchiectasis", "Carrier screening", "Family risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 84415-0 ICD-10: J47.9 Clinical summary This diagnostic test evaluates the SCNN1A gene for pathogenic variants associated with bronchiectasis and elevated sweat chloride levels.
TEST-3521 SCNN1A Gene Pseudohypoaldosteronism Type 1 Autosomal Recessive Genetic Test This test identifies mutations in the SCNN1A gene associated with autosomal recessive pseudohypoaldosteronism type 1 (PHA1). It analyzes the entire gene sequence to detect variants...	Whole blood (EDTA tube) or dried blood spot (FTA card)	21–28 working days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SCNN1A gene sequence", "Coding exons", "Splice sites"] Parameters [] Preparation ["Informed consent required", "Pre-test genetic counselling recommended"] Indications ["Infants and children presenting with salt-wasting symptoms", "Carrier screening in families with a known SCNN1A mutation"] Measurement technique Confirm with laboratory Codes LOINC: 83275-3 ICD-10: E27.40 Clinical summary This test identifies mutations in the SCNN1A gene associated with autosomal recessive pseudohypoaldosteronism type 1 (PHA1). It analyzes the entire gene sequence to detect variants causing salt-wasting.
TEST-3667 SCNN1B Gene Liddle Syndrome Genetic Test This test identifies pathogenic variants in the SCNN1B gene associated with Liddle syndrome, a cause of early-onset severe hypertension.	Whole Blood (Peripheral Venipuncture)	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 SCNN1B gene", "Single nucleotide variants", "Small insertions/deletions", "Copy Number Variations (CNV)"] Parameters [] Preparation ["No fasting required", "Provide full clinical history", "Provide prior genetic counseling records if available"] Indications ["Diagnosis of Liddle syndrome", "Evaluation of unexplained severe hypertension", "Family screening for Liddle syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 82069-3 ICD-10: I15.8, Z82.49 Clinical summary This test identifies pathogenic variants in the SCNN1B gene associated with Liddle syndrome, a cause of early-onset severe hypertension.
TEST-3760 SCO1 Gene Mutation Analysis (Hepatic Failure & Early‑Onset Neurologic Disorder) Test This test identifies pathogenic variants in the SCO1 gene associated with early-onset hepatic failure and progressive neurologic disorder.	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 ["SCO1 gene pathogenic variants", "Single nucleotide variants", "Insertions", "Deletions", "Copy-number changes"] Parameters [] Preparation ["No specific patient preparation required"] Indications ["Suspected mitochondrial hepatocerebral syndrome", "Early-onset liver disease with neurologic impairment", "Family history of SCO1-related disorder"] Measurement technique Confirm with laboratory Codes LOINC: 21660-3 ICD-10: E88.89, G31.89 Clinical summary This test identifies pathogenic variants in the SCO1 gene associated with early-onset hepatic failure and progressive neurologic disorder.
TEST-3479 SDCCAG8 Gene Senior‑Loken Syndrome Type 7 Genetic Test This genetic test evaluates the SDCCAG8 gene for pathogenic variants associated with Senior‑Loken syndrome type 7.	Whole blood (EDTA tube), extracted DNA, or FTA card	3–4 weeks (preliminary verbal result available)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the SDCCAG8 gene"] Parameters [] Preparation ["No fasting required", "Avoid alcohol and tobacco 24 hours prior"] Indications ["Suspected Senior‑Loken syndrome type 7", "Family history of ciliopathies", "Presence of renal, hepatic, and ophthalmologic findings suggestive of the syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 82939-0 ICD-10: Q87.8, Z13.71, Z84.81 Clinical summary This genetic test evaluates the SDCCAG8 gene for pathogenic variants associated with Senior‑Loken syndrome type 7.

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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