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 2761–2775 of 2,789 matching tests.

Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-2527 YWHAE Gene Miller‑Dieker Lissencephaly Syndrome Genetic Test This test analyzes the YWHAE gene for variants associated with Miller‑Dieker lissencephaly syndrome (MDLS). It provides a definitive molecular diagnosis by detecting sequence varia...	Whole Blood (EDTA), 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 ["Sequence variants in the YWHAE gene", "Small deletions/duplications in the YWHAE gene", "Known pathogenic variants associated with MDLS"] Parameters [] Preparation ["No specific dietary or medication restrictions are required.", "Fasting is not required.", "Continue all regular medications as prescribed."] Indications ["Clinical suspicion of Miller‑Dieker lissencephaly syndrome (MDLS)", "Confirmation of diagnosis based on neuroimaging (agyria/pachygyria)", "Family history of MDLS", "Prenatal diagnosis or preimplantation genetic testing"] Measurement technique Confirm with laboratory Codes LOINC: 101107-6 ICD-10: Q04.3 Clinical summary This test analyzes the YWHAE gene for variants associated with Miller‑Dieker lissencephaly syndrome (MDLS). It provides a definitive molecular diagnosis by detecting sequence variants, small deletions/duplications, and known pathogenic variants.
TEST-4569 ZAP70 Gene Selective T-cell Defect Genetic Test This test identifies pathogenic variants in the ZAP70 gene associated with severe combined immunodeficiency (SCID). It analyzes the full coding region and splice sites using Next G...	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 ZAP70 gene", "Kinase activity disruption"] Parameters [] Preparation [] Indications ["Suspected SCID", "Family history of ZAP70 mutation", "Carrier screening for first-degree relatives of confirmed proband"] Measurement technique Confirm with laboratory Codes LOINC: 74698-1 ICD-10: D81.7 Clinical summary This test identifies pathogenic variants in the ZAP70 gene associated with severe combined immunodeficiency (SCID). It analyzes the full coding region and splice sites using Next Generation Sequencing.
TEST-2711 ZBTB24 Gene ICF Syndrome Type 2 Genetic Test This diagnostic test evaluates the ZBTB24 gene for pathogenic variants associated with Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome Type 2 (ICF2).	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 ZBTB24 gene", "Single Nucleotide Variants (SNVs)", "Insertions/Deletions (indels)", "Copy Number Variants (CNVs)"] Parameters [] Preparation ["Genetic counseling session required", "Informed consent required", "Fasting is not needed"] Indications ["Suspected Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome Type 2 (ICF2)", "Recurrent infections", "Distinct facial features", "Chromosomal instability"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: D82.8 Clinical summary This diagnostic test evaluates the ZBTB24 gene for pathogenic variants associated with Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome Type 2 (ICF2).
TEST-4887 ZBTB24 Gene ICF Syndrome Type 2 Genetic Testing Test This diagnostic test evaluates the ZBTB24 gene for mutations associated with Immunodeficiency-Centromeric Instability-Facial Anomalies (ICF) Syndrome 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 ["ZBTB24 gene mutations", "Single nucleotide variants (SNVs)", "Insertions/deletions (indels)", "Splice-site alterations"] Parameters [] Preparation ["Genetic counselling session required before sample collection", "Informed consent is mandatory"] Indications ["Suspected ICF Syndrome Type 2", "Recurrent infections", "Facial dysmorphism", "Family history suggestive of ICF", "Neonates with low immunoglobulins"] Measurement technique Confirm with laboratory Codes LOINC: 92747-3 ICD-10: D81.8 Clinical summary This diagnostic test evaluates the ZBTB24 gene for mutations associated with Immunodeficiency-Centromeric Instability-Facial Anomalies (ICF) Syndrome Type 2.
TEST-4782 ZCCHC12 Gene Non‑Syndromic Intellectual Disability Genetic Test This test evaluates the ZCCHC12 gene for pathogenic variants associated with non-syndromic intellectual disability.	Peripheral Whole Blood (3-5 mL) or Saliva (2 mL)	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 ZCCHC12 gene", "Single-nucleotide variants", "Small insertions/deletions"] Parameters [] Preparation ["No fasting required", "Provide clinical history and family pedigree chart"] Indications ["Diagnosis of non-syndromic intellectual disability", "Genetic confirmation in individuals with developmental delay"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: F79 Clinical summary This test evaluates the ZCCHC12 gene for pathogenic variants associated with non-syndromic intellectual disability.
TEST-4949 ZDHHC15 Gene X‑Linked Intellectual Disability Type 91 Genetic Test This diagnostic test evaluates the ZDHHC15 gene for pathogenic variants associated with X-linked intellectual disability type 91.	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 ZDHHC15 gene coding exons", "Pathogenic variants in ZDHHC15 gene flanking splice junctions"] Parameters [] Preparation ["No specific fasting required.", "No specific medication or diet restrictions."] Indications ["Males with unexplained intellectual disability, developmental delay, or autistic features.", "Family history suggestive of X-linked inheritance.", "Females with affected male relatives (for carrier status assessment)."] Measurement technique Confirm with laboratory Codes LOINC: 94847-3 ICD-10: F78.9 Clinical summary This diagnostic test evaluates the ZDHHC15 gene for pathogenic variants associated with X-linked intellectual disability type 91.
TEST-4599 ZDHHC17 Gene Huntington Disease Genetic Test This test evaluates the ZDHHC17 gene for variants that modify the onset and progression of Huntington disease.	Whole Blood (EDTA) or 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)", "ZDHHC17 gene sequence"] Parameters [{"name": "ZDHHC17 Gene Sequence", "reference_range": null}] Preparation ["No fasting required", "Maintain normal hydration"] Indications ["Prognostic assessment in individuals with known HTT CAG expansion", "Family cascade screening for HD modifier genes", "Research-grade data for HD studies", "Evaluation of phenotypic variability in HD families"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: G10 Clinical summary This test evaluates the ZDHHC17 gene for variants that modify the onset and progression of Huntington disease.
TEST-5001 ZDHHC9 Gene Sequencing (Mental Retardation, X‑Linked Syndromic, Raymond Type) Genetic Test This test evaluates the ZDHHC9 gene for pathogenic variants associated with X-linked syndromic mental retardation (Raymond type).	Whole Blood (EDTA) or Extracted DNA	10–14 Business Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the ZDHHC9 gene", "Copy Number Variations (CNV) in the ZDHHC9 gene"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist about anticoagulant therapy"] Indications ["Suspected X-linked syndromic mental retardation (Raymond type)", "Family history of ZDHHC9-related disorders", "Genetic counselling for reproductive planning"] Measurement technique Confirm with laboratory Codes LOINC: 21624-7 ICD-10: F79 Clinical summary This test evaluates the ZDHHC9 gene for pathogenic variants associated with X-linked syndromic mental retardation (Raymond type).
TEST-2990 ZEB2 Gene Sequencing (NGS) for Congenital Central Hypoventilation Syndrome Test This test identifies pathogenic variants in the ZEB2 gene, providing a molecular diagnosis for congenital central hypoventilation syndrome (CCHS) and Mowat-Wilson syndrome.	Peripheral whole blood (EDTA tube), buccal swab, or pre-extracted genomic 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 ZEB2 gene", "Single-nucleotide variants", "Small insertions and deletions", "Splice-site alterations"] Parameters [] Preparation [] Indications ["Suspected diagnosis of congenital central hypoventilation syndrome (CCHS)", "Suspected diagnosis of Mowat-Wilson syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 97179-1 ICD-10: G47.35, Q87.89 Clinical summary This test identifies pathogenic variants in the ZEB2 gene, providing a molecular diagnosis for congenital central hypoventilation syndrome (CCHS) and Mowat-Wilson syndrome.
TEST-5554 ZFHX4 Gene (Congenital Ptosis) Genetic Test This test identifies pathogenic variants in the ZFHX4 gene associated with congenital ptosis.	Peripheral whole blood (EDTA)	3 – 4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in ZFHX4 gene", "Single nucleotide variants (SNVs)", "Insertions/deletions (indels)", "Copy number variants"] Parameters [] Preparation ["No specific fasting required", "Inform genetic counsellor about all medications and supplements"] Indications ["Diagnosis of congenital ptosis", "Genetic counselling for families with ptosis", "Differentiation of isolated vs. syndromic ptosis"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: Q10.0 Clinical summary This test identifies pathogenic variants in the ZFHX4 gene associated with congenital ptosis.
TEST-6061 ZFP57 Gene Maturity-Onset Diabetes of the Young (MODY) Sequencing Test This test identifies pathogenic mutations in the ZFP57 gene, confirming a diagnosis of ZFP57-related MODY.	Whole Blood (EDTA), 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 ZFP57 gene", "Coding exons and splice junctions of ZFP57"] Parameters [] Preparation ["No specific fasting required", "No medication or diet restrictions"] Indications ["Diagnosis of Maturity-Onset Diabetes of the Young (MODY)", "Differential diagnosis of diabetes subtypes", "Identification of ZFP57 gene mutations"] Measurement technique Confirm with laboratory Codes LOINC: 94531-1 ICD-10: E13.9 Clinical summary This test identifies pathogenic mutations in the ZFP57 gene, confirming a diagnosis of ZFP57-related MODY.
TEST-4126 ZFPM2 Gene Tetralogy of Fallot Genetic Test This test identifies genetic variants in the ZFPM2 gene associated with Tetralogy of Fallot.	Whole Blood, Extracted DNA, or One Drop Blood on FTA Card	21–28 Business Days (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 ZFPM2 gene", "Likely pathogenic variants in the ZFPM2 gene"] Parameters [] Preparation ["No fasting required", "Provide detailed clinical history", "Attend genetic counselling session (ideally)"] Indications ["Confirmation of molecular diagnosis for Tetralogy of Fallot", "Assessment of recurrence risk in future pregnancies", "Guidance for treatment planning"] Measurement technique Confirm with laboratory Codes LOINC: 82332-1 ICD-10: Q21.3 Clinical summary This test identifies genetic variants in the ZFPM2 gene associated with Tetralogy of Fallot.
TEST-5726 ZFYVE26 Gene SPG15 Genetic Test This test identifies pathogenic variants in the ZFYVE26 gene associated with Spastic Paraplegia Type 15 (SPG15).	Whole blood, extracted DNA, dried blood spot (FTA card)	21–28 business days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the ZFYVE26 gene", "Deletion/Duplication analysis of ZFYVE26"] Parameters [] Preparation [] Indications ["Diagnostic confirmation in symptomatic individuals with family history consistent with hereditary spastic paraplegia", "Confirming clinical suspicion of SPG15", "Reproductive planning in affected families"] Measurement technique Confirm with laboratory Codes LOINC: 101407-3 ICD-10: G11.4 Clinical summary This test identifies pathogenic variants in the ZFYVE26 gene associated with Spastic Paraplegia Type 15 (SPG15).
TEST-5748 ZFYVE27 Gene SPG33 Genetic Test This test identifies pathogenic variants within the ZFYVE27 gene associated with Hereditary Spastic Paraplegia type 33 (SPG33).	Peripheral whole blood (3–5 mL in EDTA tube), Extracted DNA (2 µg minimum, >50 ng/µL), or One Drop Blood 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 ["ZFYVE27 gene variants", "Pathogenic mutations"] Parameters [] Preparation ["A genetic counselling session to draw a pedigree chart of family members affected with ZFYVE27 gene SPG33 is mandatory."] Indications ["Clinical symptoms suggestive of SPG33", "Family history of autosomal dominant inheritance of SPG33"] Measurement technique Confirm with laboratory Codes LOINC: 94719-4 ICD-10: G11.4 Clinical summary This test identifies pathogenic variants within the ZFYVE27 gene associated with Hereditary Spastic Paraplegia type 33 (SPG33).
TEST-2908 ZIC1 Gene Craniosynostosis Type 6 Genetic Test This test identifies pathogenic variants in the ZIC1 gene, which are associated with craniosynostosis type 6, a condition characterized by premature fusion of skull sutures.	Whole Blood (EDTA) / Extracted DNA / FTA Card	3 to 4 Weeks from sample receipt	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ZIC1 gene sequence", "Pathogenic variants in ZIC1"] Parameters [] Preparation ["Comprehensive clinical history required", "Genetic counselling session mandatory", "Disclose all current medications, supplements, and herbal preparations"] Indications ["Suspected craniosynostosis type 6", "Family history of craniosynostosis", "Need for recurrence risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Q75.0 Clinical summary This test identifies pathogenic variants in the ZIC1 gene, which are associated with craniosynostosis type 6, a condition characterized by premature fusion of skull sutures.

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

Genetics test prices

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