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 451–465 of 805 matching tests.

Genetic diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-2502 Megalencephalic Leukoencephalopathy with Subcortical Cysts (MLC Gene Hotspot Mutation) Test This test identifies specific hotspot mutations in the MLC1 gene associated with Van der Knaap disease.	Peripheral whole blood	5 working days	1,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["MLC1 gene hotspot mutations"] Parameters [] Preparation ["No fasting or special preparation is required."] Indications ["Children with macrocephaly, motor developmental delays, or MRI evidence of subcortical cysts.", "Adults with compatible clinical and radiological features."] Measurement technique Confirm with laboratory Codes LOINC: 92838-9 ICD-10: E75.2 Clinical summary This test identifies specific hotspot mutations in the MLC1 gene associated with Van der Knaap disease.
TEST-2680 MEOX1 Gene Klippel-Feil Syndrome Type 2 Autosomal Dominant Genetic Test This test identifies pathogenic variants in the MEOX1 gene to confirm the diagnosis of Klippel-Feil syndrome type 2.	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 MEOX1 gene"] Parameters [] Preparation ["No fasting or special preparation is required."] Indications ["Early clinical diagnosis", "Familial cascade screening", "Genetic counseling", "Informed reproductive planning"] Measurement technique Confirm with laboratory Codes LOINC: 81411-9 ICD-10: Q74.0 Clinical summary This test identifies pathogenic variants in the MEOX1 gene to confirm the diagnosis of Klippel-Feil syndrome type 2.
TEST-2505 MERRF Mutation Detection Test This test detects specific pathogenic mutations in mitochondrial DNA associated with MERRF syndrome.	Peripheral whole blood	10 working days	2,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in mitochondrial DNA", "MERRF-associated mutations"] Parameters [] Preparation ["No specific fasting required.", "Do not discontinue prescribed anti-epileptic medication without consulting your doctor."] Indications ["Clinical suspicion of MERRF", "Diagnosis of mitochondrial encephalomyopathy", "Family screening for MERRF"] Measurement technique Confirm with laboratory Codes LOINC: 83991-2 ICD-10: G71.3 Clinical summary This test detects specific pathogenic mutations in mitochondrial DNA associated with MERRF syndrome.
TEST-6186 MFSD8 Gene Ceroid Lipofuscinosis Neuronal Type 7 Genetic Test This test evaluates the MFSD8 gene for pathogenic variants associated with Neuronal Ceroid Lipofuscinosis Type 7 (CLN7). It identifies mutations causing this specific neurodegenera...	Peripheral Whole Blood (EDTA) or Saliva	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 MFSD8 gene", "Coding region and conserved splice sites of the MFSD8 gene"] Parameters [] Preparation ["No fasting required", "Avoid food or drink for 30 minutes prior to buccal swab or saliva collection", "Do not brush teeth for at least 1 hour before sample collection"] Indications ["Suspected diagnosis of Neuronal Ceroid Lipofuscinosis Type 7 (CLN7)", "Family history of CLN7", "Need for definitive molecular diagnosis for genetic counselling"] Measurement technique Confirm with laboratory Codes LOINC: 47896-1 ICD-10: E75.49 Clinical summary This test evaluates the MFSD8 gene for pathogenic variants associated with Neuronal Ceroid Lipofuscinosis Type 7 (CLN7). It identifies mutations causing this specific neurodegenerative lysosomal storage disorder.
TEST-4226 MIB1 Gene LVNC7 Genetic Test This test evaluates the MIB1 gene for pathogenic variants linked to Left Ventricular Noncompaction Type 7 (LVNC7).	Peripheral whole blood or extracted DNA (3–5 mL EDTA 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 MIB1 gene", "Exon-level and splice-site variants"] Parameters [] Preparation ["Genetic counselling and informed consent are mandatory before sample collection.", "Do not discontinue prescribed cardiac medication without consulting your doctor."] Indications ["Diagnosis of suspected LVNC7", "Family risk assessment for LVNC7", "Differentiation from other cardiomyopathies"] Measurement technique Confirm with laboratory Codes LOINC: 90508-2 ICD-10: I42.8 Clinical summary This test evaluates the MIB1 gene for pathogenic variants linked to Left Ventricular Noncompaction Type 7 (LVNC7).
TEST-5328 MICU1 Gene Myopathy with Extrapyramidal Signs Genetic Test This test evaluates the entire coding region of the MICU1 gene for pathogenic variants associated with MICU1-related myopathy and extrapyramidal signs.	Peripheral whole blood (3–5 mL in EDTA tube); alternative buccal swab accepted with prior approval	3–4 weeks from sample receipt	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the MICU1 gene", "Mitochondrial calcium uptake disruption"] Parameters [] Preparation ["No fasting required", "No medication adjustments necessary", "Inform physician of anticoagulant therapy"] Indications ["Suspected MICU1-related myopathy", "Family history of MICU1-related disease", "Need for genetic confirmation"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: G71.2, G25.9 Clinical summary This test evaluates the entire coding region of the MICU1 gene for pathogenic variants associated with MICU1-related myopathy and extrapyramidal signs.
TEST-3697 MKKS Gene McKusick-Kaufman Syndrome Genetic Test This test evaluates the MKKS gene for pathogenic variants associated with McKusick-Kaufman syndrome.	Whole 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 ["Pathogenic variants in the MKKS gene", "SNVs (Single Nucleotide Variants)", "Indels (Insertions/Deletions)", "CNVs (Copy Number Variants)"] Parameters [] Preparation ["No fasting required", "No specific medication or diet restrictions"] Indications ["Clinical suspicion of McKusick-Kaufman syndrome", "Presence of hallmark features (polydactyly, hydrometrocolpos, heart defects)", "Family history of McKusick-Kaufman syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 55229-6 ICD-10: Q87.8 Clinical summary This test evaluates the MKKS gene for pathogenic variants associated with McKusick-Kaufman syndrome.
TEST-3650 MKS1 Gene (Meckel Syndrome Type 1) Genetic Test This test identifies pathogenic variants within the MKS1 gene associated with Meckel syndrome type 1.	Blood, extracted DNA, or FTA card specimen	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 MKS1 gene", "Exons and splice sites of the MKS1 gene"] Parameters [] Preparation ["Pre-test genetic counselling session required", "Schedule session via WhatsApp at +971 54 548 8731"] Indications ["Individuals with suggestive prenatal ultrasound findings", "Individuals with a family history of the condition"] Measurement technique Confirm with laboratory Codes LOINC: 81278-7 ICD-10: Q61.9 Clinical summary This test identifies pathogenic variants within the MKS1 gene associated with Meckel syndrome type 1.
TEST-4767 MLC1 Gene Megalencephalic Leukoencephalopathy with Subcortical Cysts Genetic Test This genetic test detects pathogenic variants in the MLC1 gene associated with Megalencephalic Leukoencephalopathy with Subcortical Cysts (MLC).	Whole Blood, Extracted DNA, 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 MLC1 gene"] Parameters [] Preparation [] Indications ["Clinical suspicion of MLC", "Neurological decline", "Macrocephaly"] Measurement technique Confirm with laboratory Codes LOINC: 94233-3 ICD-10: E75.21 Clinical summary This genetic test detects pathogenic variants in the MLC1 gene associated with Megalencephalic Leukoencephalopathy with Subcortical Cysts (MLC).
TEST-1972 MLH1 Gene Genetic Test for Muir-Torre Syndrome This test evaluates the MLH1 gene for mutations associated with hereditary cancer predisposition syndromes like Lynch syndrome and Muir-Torre syndrome.	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 MLH1 gene", "Single nucleotide variants (SNVs)", "Insertions/deletions (Indels)", "Copy number variations (CNVs)"] Parameters [] Preparation ["No special preparation is needed."] Indications ["Individuals with a personal or family history suggestive of Lynch syndrome or Muir-Torre syndrome.", "Screening for hereditary cancer predisposition."] Measurement technique Confirm with laboratory Codes LOINC: 82533-7 ICD-10: Z15.89, Z80.0, Z12.11 Clinical summary This test evaluates the MLH1 gene for mutations associated with hereditary cancer predisposition syndromes like Lynch syndrome and Muir-Torre syndrome.
TEST-5989 MMACHC Gene Methylmalonic Aciduria CblC Type Genetic Test This genetic test identifies pathogenic variants in the MMACHC gene associated with methylmalonic aciduria and homocystinuria, cblC type.	Whole Blood (EDTA) 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 MMACHC gene", "Single nucleotide variants", "Insertions", "Deletions", "Splice-site alterations"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed vitamin B12, betaine, or dietary supplements"] Indications ["Confirmation of diagnosis in individuals with suggestive biochemical findings", "Carrier status determination in at-risk family members", "Prenatal planning for couples with known familial pathogenic variants"] Measurement technique Confirm with laboratory Codes LOINC: 86565-2 ICD-10: E71.1 Clinical summary This genetic test identifies pathogenic variants in the MMACHC gene associated with methylmalonic aciduria and homocystinuria, cblC type.
TEST-5177 MMP1 Gene (Epidermolysis Bullosa Dystrophica Modifier) Genetic Test This genetic test identifies variants in the MMP1 gene that modify the severity of autosomal recessive dystrophic epidermolysis bullosa (RDEB).	Whole Blood, Dried Blood Spot (FTA Card), Extracted DNA	3 – 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["MMP1 gene variants", "Genetic modifiers influencing RDEB severity"] Parameters [] Preparation ["Pre-test genetic counselling session required before sample collection"] Indications ["Diagnosis of RDEB", "Carrier screening for RDEB", "Prognosis assessment in RDEB", "Unclear diagnosis of blistering disorders"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Q81.2 Clinical summary This genetic test identifies variants in the MMP1 gene that modify the severity of autosomal recessive dystrophic epidermolysis bullosa (RDEB).
TEST-2774 MMP21 Gene Heterotaxy, Visceral Type 7 Test This test identifies pathogenic variants in the MMP21 gene associated with heterotaxy visceral type 7, a congenital disorder affecting organ arrangement.	Whole blood (EDTA), 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 ["MMP21 gene coding region", "Splice junctions (± 20 bp)"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any recent blood transfusions"] Indications ["Suspected heterotaxy visceral type 7", "Congenital laterality disorder", "Family history of MMP21-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 21669-6 ICD-10: Q89.3 Clinical summary This test identifies pathogenic variants in the MMP21 gene associated with heterotaxy visceral type 7, a congenital disorder affecting organ arrangement.
TEST-5960 MPC1 Gene Mitochondrial Pyruvate Carrier Deficiency Genetic Test This genetic test evaluates the entire coding region of the MPC1 gene for pathogenic variants associated with mitochondrial pyruvate carrier deficiency.	Whole Blood, Extracted DNA, or Dried Blood Spot (DBS) on 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 MPC1 gene", "Copy Number Variations (CNV) in the MPC1 gene"] Parameters [] Preparation ["Stabilize medically before sample collection if in acute metabolic decompensation"] Indications ["Suspected mitochondrial pyruvate carrier deficiency", "Family history of metabolic disorders"] Measurement technique Confirm with laboratory Codes LOINC: 21636-7 ICD-10: E74.89 Clinical summary This genetic test evaluates the entire coding region of the MPC1 gene for pathogenic variants associated with mitochondrial pyruvate carrier deficiency.
TEST-6321 MPI Gene Glycosylation Disorder Type 1B Genetic Test This genetic test identifies pathogenic variants in the MPI gene associated with Congenital Disorder of Glycosylation Type 1B (CDG-Ib).	Whole Blood (EDTA), Extracted DNA, or Dried Blood Spot on 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 MPI gene", "Single nucleotide variants (SNVs)", "Small insertions and deletions (indels)", "Copy number variants (CNVs)", "Deep intronic splice-site alterations"] Parameters [] Preparation ["Mandatory pre-test genetic counselling", "Provide pedigree chart documentation"] Indications ["Suspected Congenital Disorder of Glycosylation Type 1B (CDG-Ib)", "Unexplained protein-losing enteropathy", "Congenital hepatic fibrosis", "Family history of CDG-Ib"] Measurement technique Confirm with laboratory Codes LOINC: 94233-5 ICD-10: E77.8 Clinical summary This genetic test identifies pathogenic variants in the MPI gene associated with Congenital Disorder of Glycosylation Type 1B (CDG-Ib).

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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