Diagnostic options · UAE

Genetic tests in Dubai & UAE

Compare available Genetic 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

805

Listed price range

600.00–30,000.00 AED

Clinical preparation

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Genetic test prices

Showing 226–240 of 805 matching tests.

Genetic diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-5257 DSPP Gene Dentinogenesis Imperfecta Shields Type 3 Genetic Test This genetic test identifies pathogenic variants in the DSPP gene associated with Dentinogenesis Imperfecta Shields Type 3.	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 ["DSPP gene pathogenic variants", "Single nucleotide variants (SNVs)", "Small insertions and deletions (indels)", "Splice-site alterations"] Parameters [] Preparation ["No fasting or dietary preparation required", "Provide a complete list of current medications and supplements"] Indications ["Clinical suspicion of Dentinogenesis Imperfecta Shields Type 3", "Family history of the disorder", "Recurrence risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 94299-7 ICD-10: K00.5 Clinical summary This genetic test identifies pathogenic variants in the DSPP gene associated with Dentinogenesis Imperfecta Shields Type 3.
TEST-4330 DST Gene (Epidermolysis Bullosa Simplex, Autosomal Recessive Type 2) Genetic Test This genetic test identifies pathogenic variants in the DST gene, confirming a diagnosis of autosomal recessive epidermolysis bullosa simplex type 2.	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 DST gene"] Parameters [] Preparation ["No fasting required", "Provide a fresh whole blood sample", "Be ready to share a detailed three-generation family history"] Indications ["Suspected autosomal recessive epidermolysis bullosa simplex type 2", "Family history of epidermolysis bullosa simplex"] Measurement technique Confirm with laboratory Codes LOINC: 81413-0 ICD-10: Q81.0 Clinical summary This genetic test identifies pathogenic variants in the DST gene, confirming a diagnosis of autosomal recessive epidermolysis bullosa simplex type 2.
TEST-6250 DYM Gene Dyggve-Melchior-Clausen Disease Genetic Test This test evaluates the DYM gene for mutations associated with Dyggve-Melchior-Clausen syndrome.	Peripheral Whole Blood	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["DYM gene coding exons", "Flanking intronic regions"] Parameters [] Preparation [] Indications ["Establishing a definitive diagnosis in symptomatic children", "Carrier screening for family planning", "Guiding early therapeutic interventions"] Measurement technique Confirm with laboratory Codes LOINC: 16994-7 ICD-10: Q87.1 Clinical summary This test evaluates the DYM gene for mutations associated with Dyggve-Melchior-Clausen syndrome.
TEST-4948 DYRK1A Gene Sequencing (Autosomal Dominant Intellectual Disability 7) 2800 AED Test This diagnostic test evaluates the DYRK1A gene for sequence variants (SNVs, indels) and copy number variations (CNVs) associated with Autosomal Dominant Intellectual Disability typ...	Peripheral Whole Blood (EDTA) or Buccal Swab (FTA Card)	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Single Nucleotide Variants (SNVs)", "Insertions/Deletions (Indels)", "Copy Number Variations (CNVs)"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any current medications"] Indications ["Suspected Autosomal Dominant Intellectual Disability type 7", "Neurodevelopmental delay of unknown etiology", "Family history of DYRK1A-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 104621-5 ICD-10: F78, R41.83 Clinical summary This diagnostic test evaluates the DYRK1A gene for sequence variants (SNVs, indels) and copy number variations (CNVs) associated with Autosomal Dominant Intellectual Disability type 7.
TEST-5341 DYSF Gene Myopathy, Distal with Anterior Tibial Onset Genetic Test This genetic test identifies pathogenic variants in the DYSF gene associated with distal myopathy and LGMD2B.	Peripheral 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 DYSF gene", "Copy number variations within the DYSF gene"] Parameters [] Preparation ["No specific fasting required", "Inform the lab of any medications being taken"] Indications ["Suspected diagnosis of distal myopathy with anterior tibial onset (Miyoshi myopathy)", "Suspected diagnosis of Limb-Girdle Muscular Dystrophy Type 2B (LGMD2B)", "Family history of dysferlinopathy", "Evaluation of individuals with unexplained progressive muscle weakness"] Measurement technique Confirm with laboratory Codes LOINC: 81263-6 ICD-10: G71.0 Clinical summary This genetic test identifies pathogenic variants in the DYSF gene associated with distal myopathy and LGMD2B.
TEST-2997 ECE1 Gene Central Hypoventilation Syndrome Congenital Genetic Test This test identifies mutations in the ECE1 gene associated with congenital central hypoventilation syndrome.	Peripheral whole blood, dried blood spot on FTA card, or extracted genomic DNA	3 to 4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Mutations in the ECE1 gene"] Parameters [] Preparation ["No specific fasting required", "Ensure patient is stable if ventilator-dependent"] Indications ["Suspected congenital central hypoventilation syndrome", "Newborns/children with unexplained respiratory issues"] Measurement technique Confirm with laboratory Codes LOINC: 94043-0 ICD-10: G47.35 Clinical summary This test identifies mutations in the ECE1 gene associated with congenital central hypoventilation syndrome.
TEST-5403 ECEL1 Gene Arthrogryposis, Distal, Type 5D Genetic Test This test evaluates the ECEL1 gene for variants associated with Distal Arthrogryposis Type 5D.	Peripheral Whole Blood	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ECEL1 gene sequence", "Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Copy number variations (CNVs)"] Parameters [] Preparation ["No specific fasting required", "Do not alter medications without physician consultation"] Indications ["Suspected Distal Arthrogryposis Type 5D", "Family history of Distal Arthrogryposis Type 5D"] Measurement technique Confirm with laboratory Codes LOINC: 94306-8 ICD-10: Q74.3, Q68.8 Clinical summary This test evaluates the ECEL1 gene for variants associated with Distal Arthrogryposis Type 5D.
TEST-5126 ECHS1 Gene Enoyl‑CoA Hydratase 1 Deficiency Genetic Test This test analyzes the ECHS1 gene for pathogenic variants associated with mitochondrial short-chain enoyl-CoA hydratase 1 deficiency.	Whole blood (EDTA), buccal swab, 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 ECHS1 gene", "Mitochondrial fatty acid oxidation defect"] Parameters [] Preparation ["Do not discontinue prescribed medications without consulting the managing physician", "Genetic counselling is required before sample collection"] Indications ["Suspected mitochondrial fatty acid oxidation defect", "Patients with neurological symptoms suggestive of ECHS1 deficiency"] Measurement technique Confirm with laboratory Codes LOINC: 81307-7 ICD-10: E71.39 Clinical summary This test analyzes the ECHS1 gene for pathogenic variants associated with mitochondrial short-chain enoyl-CoA hydratase 1 deficiency.
TEST-5817 ECM1 Gene Analysis for Urbach-Wiethe Disease Test This test evaluates the ECM1 gene for pathogenic variants associated with Urbach-Wiethe disease (lipoid proteinosis). It utilizes Next-Generation Sequencing (NGS) for comprehensive...	Peripheral Whole Blood (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 ECM1 gene", "Single Nucleotide Variants (SNVs)", "Insertions/Deletions (indels)", "Copy Number Changes (CNVs)"] Parameters [] Preparation ["Pre-test genetic counselling is mandatory", "No specific fasting required for blood draw"] Indications ["Clinical suspicion of Urbach-Wiethe disease", "Family history of lipoid proteinosis", "Carrier screening in at-risk individuals"] Measurement technique Confirm with laboratory Codes LOINC: 94850-1 ICD-10: E78.89 Clinical summary This test evaluates the ECM1 gene for pathogenic variants associated with Urbach-Wiethe disease (lipoid proteinosis). It utilizes Next-Generation Sequencing (NGS) for comprehensive analysis.
TEST-5223 EDAR Gene Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive Genetic Test This genetic test analyzes the entire EDAR gene to detect mutations associated with hypohidrotic ectodermal dysplasia (HED). It identifies variants that affect the development of e...	Blood, Extracted DNA, or One-drop Blood on FTA Card	3-4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["EDAR gene sequence", "Mutations (variants) within the EDAR gene", "Copy number variants (deletions/duplications) in the EDAR gene"] Parameters [] Preparation ["No specific fasting required.", "Inform the lab about any recent blood transfusions (within 2 weeks)."] Indications ["Suspected diagnosis of hypohidrotic ectodermal dysplasia (HED)", "Family history of HED", "Need for genetic counseling and family planning related to HED"] Measurement technique Confirm with laboratory Codes LOINC: 95121-8 ICD-10: Q82.4 Clinical summary This genetic test analyzes the entire EDAR gene to detect mutations associated with hypohidrotic ectodermal dysplasia (HED). It identifies variants that affect the development of ectodermal structures like teeth, sweat glands, hair, and skin.
TEST-2773 EDNRB Gene Hirschsprung Disease Genetic Test This test evaluates the EDNRB gene for pathogenic variants associated with Hirschsprung disease.	Blood, Extracted DNA, FTA Card 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 EDNRB gene", "Single nucleotide variants", "Insertions", "Deletions", "Splice-site alterations"] Parameters [] Preparation ["Provide detailed clinical history", "Provide a three-generation pedigree chart", "Genetic counseling session mandatory for minors"] Indications ["Clinical and radiological findings suggesting aganglionosis", "Suspicion of Hirschsprung disease"] Measurement technique Confirm with laboratory Codes LOINC: 77640-3 ICD-10: Q43.1, Z14.8, Z13.79 Clinical summary This test evaluates the EDNRB gene for pathogenic variants associated with Hirschsprung disease.
TEST-4364 EFHC1 Gene Juvenile Absence Epilepsy Type 1 DNA Test This test identifies pathogenic variants in the EFHC1 gene associated with juvenile absence epilepsy type 1.	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 EFHC1 gene", "Point mutations", "Small indels"] Parameters [] Preparation [] Indications ["Diagnosis of juvenile absence epilepsy type 1 (JAE)", "Familial risk assessment for JAE", "Personalized antiepileptic management"] Measurement technique Confirm with laboratory Codes LOINC: 91849-1 ICD-10: G40.A01 Clinical summary This test identifies pathogenic variants in the EFHC1 gene associated with juvenile absence epilepsy type 1.
TEST-4784 EIF2B2 Gene Leukoencephalopathy with Vanishing White Matter (VWM) Genetic Test This test identifies pathogenic variants in the EIF2B2 gene associated with leukoencephalopathy with vanishing white matter.	Peripheral Whole Blood or FTA Card (Fingerstick)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["EIF2B2 gene sequence", "Pathogenic variants in EIF2B2"] Parameters [] Preparation ["No specific fasting required", "Avoid testing if active infection is present"] Indications ["Molecular confirmation of suspected VWM", "Carrier screening in at-risk family members", "Reproductive risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 101398-1 ICD-10: G93.81 Clinical summary This test identifies pathogenic variants in the EIF2B2 gene associated with leukoencephalopathy with vanishing white matter.
TEST-6240 ELAC2 Gene Combined Oxidative Phosphorylation Deficiency Type 17 Genetic Test This genetic test identifies mutations in the ELAC2 gene associated with Combined Oxidative Phosphorylation Deficiency Type 17.	Peripheral whole blood; pre-extracted DNA	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ELAC2 gene mutations", "Combined Oxidative Phosphorylation Deficiency Type 17"] Parameters [] Preparation ["No fasting or special preparation required"] Indications ["Suspected Combined Oxidative Phosphorylation Deficiency Type 17", "Family history of mitochondrial disorders"] Measurement technique Confirm with laboratory Codes LOINC: 81304-2 ICD-10: E74.810 Clinical summary This genetic test identifies mutations in the ELAC2 gene associated with Combined Oxidative Phosphorylation Deficiency Type 17.
TEST-4947 ELOVL4 Gene: Ichthyosis, Spastic Quadriplegia, and Intellectual Disability Test This test evaluates the ELOVL4 gene for pathogenic variants associated with a specific syndromic disorder.	Peripheral whole blood (3-5 mL EDTA) or dried blood spot on 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 ELOVL4 gene coding region", "Pathogenic variants in ELOVL4 gene splice sites"] Parameters [] Preparation ["Pre-test genetic counselling is mandatory.", "Informed consent must be signed."] Indications ["Suspected ELOVL4-related disorder", "Family history of ELOVL4-related disorder", "Genetic counseling for reproductive planning"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Q80.8 Clinical summary This test evaluates the ELOVL4 gene for pathogenic variants associated with a specific syndromic disorder.

Category overview

Genetic: overview

Unlocking the blueprint of your DNA provides profound, proactive insights into your family’s future and personal health risks. Integrated within our advanced Biochemistry and molecular services, specialized Genetic testing evaluates inherited traits, metabolic predispositions, and carrier statuses. Utilizing cutting-edge diagnostic technology, comprehensive genetic screening offers the vital clarity needed to safely guide tailored medical strategies and family planning. As an undisputed leader in innovation among diagnostic labs in Dubai and the UAE, DNA Labs guarantees the highest standards of strict patient confidentiality, unparalleled diagnostic precision, and rapid reporting. Empower your health decisions with certainty—book your genetic testing in UAE, coordinate a secure sample collection, or connect with our specialized genetics team today.

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The right diagnostic option depends on your reason for testing and individual circumstances. Check the listed specimen and timing, then confirm any preparation requirements with the ordering clinician or laboratory before collection.