Diagnostic options · UAE

Genetics tests in Dubai & UAE

Compare available Genetics 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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2,789

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-1.00–50,000.00 AED

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Genetics test prices

Showing 106–120 of 2,789 matching tests.

Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-5271 ALDH18A1 Gene (Cutis Laxa Type 3A, Autosomal Recessive) Genetic Test This genetic test evaluates the ALDH18A1 gene for mutations associated with autosomal recessive cutis laxa type 3A (ARCL3A). It identifies disease-causing variants to confirm the d...	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 ["ALDH18A1 gene sequence", "Disease-causing mutations"] Parameters [{"name": "Coverage", "reference_range": "Full ALDH18A1 gene (all exons and flanking regions)"}, {"name": "Sensitivity", "reference_range": ">99.9% (NGS with >1000x depth)"}] Preparation ["No specific fasting required", "Do not discontinue prescribed medication"] Indications ["Suspected diagnosis of autosomal recessive cutis laxa type 3A", "Family history of ARCL3A"] Measurement technique Confirm with laboratory Codes LOINC: 21639-0 ICD-10: Q82.8 Clinical summary This genetic test evaluates the ALDH18A1 gene for mutations associated with autosomal recessive cutis laxa type 3A (ARCL3A). It identifies disease-causing variants to confirm the diagnosis.
TEST-4098 ALDH1A2 Gene Tetralogy of Fallot Genetic Test This test identifies pathogenic variants in the ALDH1A2 gene associated with Tetralogy of Fallot.	Peripheral whole blood (EDTA tube)	3–4 weeks (21–28 days)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the ALDH1A2 gene", "DNA sequence analysis of the ALDH1A2 gene"] Parameters [] Preparation ["No specific fasting required", "No medication adjustments needed unless advised by physician"] Indications ["Diagnosis of Tetralogy of Fallot", "Risk assessment for familial inheritance", "Prenatal diagnosis", "Pre-surgical planning"] Measurement technique Confirm with laboratory Codes LOINC: 94735-5 ICD-10: Q21.3 Clinical summary This test identifies pathogenic variants in the ALDH1A2 gene associated with Tetralogy of Fallot.
TEST-5597 ALDH3A2 Gene Sjögren-Larsson Syndrome Genetic Test This test evaluates the ALDH3A2 gene for pathogenic variants associated with Sjögren-Larsson syndrome.	Peripheral whole blood (3-5 mL in EDTA vacutainer)	21 calendar days (standard) / 10 calendar days (expedited)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in ALDH3A2 gene", "Coding exons and flanking intronic regions"] Parameters [] Preparation ["No fasting required", "Disclose current medications (especially anticoagulants)", "Disclose blood transfusions within 4 weeks"] Indications ["Clinical suspicion of Sjögren-Larsson syndrome", "Triad of scaly skin from birth, delayed motor milestones, and spasticity"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: Q87.8 Clinical summary This test evaluates the ALDH3A2 gene for pathogenic variants associated with Sjögren-Larsson syndrome.
TEST-5877 ALDH5A1 Gene Succinic Semialdehyde Dehydrogenase Deficiency Genetic Test This genetic test identifies mutations in the ALDH5A1 gene responsible for succinic semialdehyde dehydrogenase (SSADH) deficiency.	Peripheral whole blood (EDTA tube)	3 to 4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ALDH5A1 gene mutations", "Single nucleotide variants", "Small indels", "Exon-level copy number changes"] Parameters [] Preparation ["No special preparation such as fasting is required."] Indications ["Suspected SSADH deficiency based on clinical presentation", "Confirmation of diagnosis", "Family planning for autosomal recessive disorders"] Measurement technique Confirm with laboratory Codes LOINC: 90521-1 ICD-10: E72.8 Clinical summary This genetic test identifies mutations in the ALDH5A1 gene responsible for succinic semialdehyde dehydrogenase (SSADH) deficiency.
TEST-5640 ALDH7A1 Gene Pyridoxine‑Dependent Epilepsy Genetic Test This genetic test detects pathogenic variants in the ALDH7A1 gene associated with pyridoxine-dependent epilepsy.	Whole Blood, Dried Blood Spot (FTA card), Extracted Genomic DNA (gDNA)	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 ALDH7A1 gene", "Single Nucleotide Variants (SNVs)", "Insertions/Deletions (indels)", "Copy Number Variants (CNVs)"] Parameters [] Preparation ["No fasting required", "No medication changes required"] Indications ["Infants with early-onset seizures unresponsive to standard anticonvulsants", "Children with unexplained recurrent seizures", "Family members with a known ALDH7A1 variant"] Measurement technique Confirm with laboratory Codes LOINC: 92736-3 ICD-10: G40.42 Clinical summary This genetic test detects pathogenic variants in the ALDH7A1 gene associated with pyridoxine-dependent epilepsy.
TEST-6381 ALDOA Gene Glycogen Storage Disease Type 12 (GSD XII) Genetic Test This genetic test identifies pathogenic variants in the ALDOA gene associated with Glycogen Storage Disease Type 12 (GSD XII).	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 ["Pathogenic variants in the ALDOA gene", "Coding region and splice junctions of the ALDOA gene"] Parameters [] Preparation ["Mandatory pre-test genetic counselling session", "No fasting or medication changes unless directed by physician"] Indications ["Clinical suspicion of GSD XII", "Unexplained haemolysis with myopathy", "Positive family history of GSD XII"] Measurement technique Confirm with laboratory Codes LOINC: 82847-5 ICD-10: E74.09 Clinical summary This genetic test identifies pathogenic variants in the ALDOA gene associated with Glycogen Storage Disease Type 12 (GSD XII).
TEST-6382 ALDOB Gene Hereditary Fructose Intolerance (HFI) Genetic Test This genetic test identifies disease-causing variants in the ALDOB gene, confirming hereditary fructose intolerance (HFI). It assesses the entire coding region and splice sites for...	Whole Blood (3 mL) or FTA Micro-Collection Card	3 – 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ALDOB gene sequence", "Pathogenic variants in ALDOB gene"] Parameters [] Preparation ["Detailed clinical history recording required", "Mandatory genetic counselling session", "Three-generation pedigree documentation"] Indications ["Clinical suspicion of hereditary fructose intolerance", "Family history of HFI or unexplained liver disease", "Need for definitive molecular diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 94228-2 ICD-10: E74.12 Clinical summary This genetic test identifies disease-causing variants in the ALDOB gene, confirming hereditary fructose intolerance (HFI). It assesses the entire coding region and splice sites for mutations.
TEST-6361 ALG1 Gene Glycosylation Disorder Type 1K Genetic Test This test detects pathogenic variants in the ALG1 gene associated with Congenital Disorder of Glycosylation Type Ik (CDG-Ik).	Whole Blood (EDTA), Extracted DNA, or Dried Blood Spot (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 ALG1 gene", "Single nucleotide variants", "Small insertions and deletions", "Splice-site mutations"] Parameters [] Preparation ["No fasting required.", "Complete a pre-test genetic counselling session.", "Provide a detailed three-generation family pedigree chart."] Indications ["Clinical suspicion of CDG-Ik", "Evaluation of rare inborn errors of metabolism"] Measurement technique Confirm with laboratory Codes LOINC: 50398-0 ICD-10: E77.8 Clinical summary This test detects pathogenic variants in the ALG1 gene associated with Congenital Disorder of Glycosylation Type Ik (CDG-Ik).
TEST-6273 ALG11 Gene Congenital Disorder of Glycosylation Type Ip (CDG‑Ip) Genetic Test This genetic test identifies pathogenic variants in the ALG11 gene associated with congenital disorder of glycosylation type Ip (CDG‑Ip).	Whole Blood (EDTA) 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 ALG11 gene"] Parameters [] Preparation [] Indications ["Suspected congenital disorder of glycosylation type Ip (CDG‑Ip)", "Family history of CDG‑Ip"] Measurement technique Confirm with laboratory Codes LOINC: 94068-7 ICD-10: E77.8, Z13.228, Z84.81 Clinical summary This genetic test identifies pathogenic variants in the ALG11 gene associated with congenital disorder of glycosylation type Ip (CDG‑Ip).
TEST-6293 ALG13 Gene Glycosylation Disorder Type 1S Genetic Test This test identifies pathogenic variants within the ALG13 gene associated with Congenital Disorder of Glycosylation Type 1S (CDG-1S).	Whole Blood (EDTA), Extracted DNA, or One‑Drop Blood on FTA Card	3 to 4 Weeks (including confirmatory analysis)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the ALG13 gene", "Congenital Disorder of Glycosylation Type 1S (CDG-1S)"] Parameters [] Preparation ["Mandatory genetic counselling session required before sample collection", "No fasting required", "Inform lab of recent blood transfusion ( Indications ["Suspected Congenital Disorder of Glycosylation Type 1S (CDG-1S)", "Patients with clinical features suggestive of CDG-1S", "Family history of CDG-1S"] Measurement technique Confirm with laboratory Codes LOINC: 92651-7 ICD-10: E77.8 Clinical summary This test identifies pathogenic variants within the ALG13 gene associated with Congenital Disorder of Glycosylation Type 1S (CDG-1S).
TEST-6318 ALG3‑Congenital Disorder of Glycosylation Type Id (CDG‑Id) Genetic Test This test detects pathogenic variants in the ALG3 gene associated with Congenital Disorder of Glycosylation Type Id (CDG-Id).	Whole Blood (EDTA) 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 ALG3 gene", "Single nucleotide variants", "Small insertions/deletions", "Copy-number changes"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Suspected Congenital Disorder of Glycosylation Type Id (CDG-Id)", "Family history of CDG-Id", "Evaluation of rare metabolic disorders"] Measurement technique Confirm with laboratory Codes LOINC: 77637-8 ICD-10: E74.89, Z13.79, Z14.9 Clinical summary This test detects pathogenic variants in the ALG3 gene associated with Congenital Disorder of Glycosylation Type Id (CDG-Id).
TEST-6309 ALG8 Gene (Congenital Disorder of Glycosylation Type Ih) Genetic Test This genetic test identifies inherited mutations in the ALG8 gene associated with Congenital Disorder of Glycosylation Type Ih (CDG-1h).	Whole Blood (Venipuncture 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 ALG8 gene", "Glycoprotein synthesis pathway defects"] Parameters [] Preparation ["Pre-test genetic counselling is mandatory.", "Document a three-generation pedigree."] Indications ["Suspected Congenital Disorder of Glycosylation Type Ih (CDG-1h)", "Family history of CDG-1h", "Unexplained multi-systemic symptoms suggestive of a metabolic disorder"] Measurement technique Confirm with laboratory Codes LOINC: 96021-5 ICD-10: E74.8, Z13.79, Z15.89 Clinical summary This genetic test identifies inherited mutations in the ALG8 gene associated with Congenital Disorder of Glycosylation Type Ih (CDG-1h).
TEST-2506 ALK Gene (Neuroblastoma Type 3, Familial) Susceptibility NGS Test This test evaluates the ALK gene for hereditary mutations associated with familial neuroblastoma type 3.	Whole Blood, Extracted DNA, or Fingerpick FTA Card	12 Business Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ALK gene mutations", "Single nucleotide variants", "Small insertions/deletions"] Parameters [] Preparation ["Genetic counselling required prior to testing"] Indications ["Families with early-onset tumors", "Multiple affected relatives", "Known ALK-related syndromes", "Pre-test genetic counselling"] Measurement technique Confirm with laboratory Codes LOINC: 74057-6 ICD-10: C74.91, Z80.6 Clinical summary This test evaluates the ALK gene for hereditary mutations associated with familial neuroblastoma type 3.
TEST-1870 ALK/EML4 (NSCLC) Gene Rearrangement Test This test detects the presence of ALK/EML4 gene rearrangements in tumor tissue using FISH technology.	Formalin-Fixed Paraffin-Embedded (FFPE) Tumor Tissue Block or Unstained Slides	4–5 Working Days	1,400.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ALK gene rearrangements", "EML4 gene rearrangements", "Fusion events"] Parameters [] Preparation ["No specific fasting or dietary preparation required", "Valid doctor's prescription is mandatory"] Indications ["Diagnosis of non-small cell lung carcinoma (NSCLC)", "Guidance for targeted therapy selection in NSCLC"] Measurement technique Confirm with laboratory Codes LOINC: 62458-1 ICD-10: C34.9 Clinical summary This test detects the presence of ALK/EML4 gene rearrangements in tumor tissue using FISH technology.
TEST-4956 ALOX12B Gene Sequencing for Autosomal Recessive Congenital Ichthyosis Type 2 (Genetic Test) This genetic test detects pathogenic variants in the ALOX12B gene associated with autosomal recessive congenital ichthyosis type 2 (ARCI2).	Peripheral Whole Blood (EDTA), FTA Card Spot, 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 ALOX12B gene"] Parameters [] Preparation [] Indications ["Confirmation of ARCI2 diagnosis", "Genetic counselling for families", "Carrier status assessment for family planning"] Measurement technique Confirm with laboratory Codes LOINC: 94471-6 ICD-10: Q80.2 Clinical summary This genetic test detects pathogenic variants in the ALOX12B gene associated with autosomal recessive congenital ichthyosis type 2 (ARCI2).

Category overview

Genetics: overview

Understanding your unique biological blueprint offers a profound sense of clarity and empowers proactive health planning for you and your family. At DNA Labs UAE, our specialized Genetics division employs state-of-the-art molecular technologies to provide deep insights into hereditary markers and cellular mutations. This comprehensive genetics testing in the UAE equips your healthcare provider with the precise data needed to tailor your medical guidance effectively. Recognized among top diagnostic labs in Dubai and the UAE, we prioritize your peace of mind through strict confidentiality protocols and exceptionally fast, accurate reporting. Take the next step in your health journey. View our genetics diagnostic services, book a private home collection, or consult our specialized team today.

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Genetics tests in Dubai & UAE

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