Genetics
Inherited Disorders Tests in Dubai & UAE
Investigations in this area, with the specimen type, turnaround time and listed price for each option — so you and your clinician can compare before you book.
- Quality-controlled laboratory
- Home collection across the UAE
- Confidential handling of results
Compare options
Inherited Disorders investigations
All 10 investigations in this category are listed below.
| Test | What it measures | Specimen | Turnaround | Price | Book |
|---|---|---|---|---|---|
| ABCD1 Gene Adrenoleukodystrophy (X-Linked) Test TEST-3730 LOINC 93119-6 | This test analyzes the ABCD1 gene to detect pathogenic variants associated with X-linked adrenoleukodystrophy (X-ALD). It provides definitive diagnosi... | Peripheral Whole Blood (EDTA) | 3–4 Weeks | 2,800.00 AED | Details |
| BCHE Gene Butyrylcholinesterase Deficiency Genetic Test TEST-6051 LOINC 21671-0 | This genetic test evaluates the BCHE gene for mutations associated with butyrylcholinesterase deficiency, an inherited condition affecting anesthetic... | Whole Blood, Extracted DNA, Dried Blood Spot (FTA Card) | 3–4 Weeks (21–28 Calendar Days) | 2,800.00 AED | Details |
| MANBAL Gene (Mannosidosis, Beta A, Lysosomal) Genetic Test TEST-6048 LOINC 83136-1 | This genetic test identifies pathogenic variants in the MANBA gene associated with Beta-Mannosidosis. | Whole Blood (EDTA tube), Buccal Swab, FTA Card, or Extracted DNA | 3 to 4 Weeks | 2,800.00 AED | Details |
| NLRP3 Gene Muckle-Wells Syndrome Genetic Test TEST-4794 LOINC 96410-7 | This test identifies pathogenic variants in the NLRP3 gene associated with Muckle-Wells Syndrome. | Whole blood (EDTA), extracted DNA, or FTA card | 3–4 weeks | 2,800.00 AED | Details |
| Noonan-RASopathies Panel Genetic Test TEST-3106 LOINC 92718-9 | This test identifies germline mutations in 22 genes associated with RASopathies, including Noonan syndrome and neurofibromatosis type 1. | Whole Blood (EDTA, 3-5 mL), Extracted DNA (≥1 µg), or FTA Card | 3 to 4 Weeks | 3,000.00 AED | Details |
| NOTCH2 Gene Alagille Syndrome Type 2 Genetic Test TEST-3086 LOINC 94391-3 | This genetic test analyzes the NOTCH2 gene to identify mutations associated with Alagille syndrome type 2. | Peripheral Whole Blood (EDTA) or Extracted Genomic DNA | 21-28 Days (Expedited options available) | 2,800.00 AED | Details |
| NSDHL Gene CHILD Syndrome Genetic Test (NGS) TEST-4044 LOINC 21621-4 | This test detects pathogenic variants in the NSDHL gene to confirm a diagnosis of CHILD syndrome. | Peripheral whole blood (EDTA tube) | 3–4 weeks | 2,800.00 AED | Details |
| POLR1C Gene Treacher Collins Syndrome Type 3 Genetic Test TEST-2227 LOINC 81266-1 | This test evaluates the POLR1C gene for pathogenic variants associated with Treacher Collins syndrome type 3 (TCS3). It uses Next-Generation Sequencin... | Peripheral whole blood (3–5 mL in EDTA tube), FTA card, or extracted DNA | 3–4 weeks | 2,800.00 AED | Details |
| RFX5 Gene (Bare Lymphocyte Syndrome Type 2) Genetic Test TEST-3350 LOINC 21668-8 | This test identifies pathogenic variants in the RFX5 gene associated with Bare Lymphocyte Syndrome Type 2 (MHC Class II Deficiency), a severe combined... | Peripheral Whole Blood (Venipuncture) or Dried Blood Spot (FTA Card) | 3–4 Weeks (21–28 Business Days) | 2,800.00 AED | Details |
| SCNN1G Gene Liddle Syndrome Genetic Test (NGS) TEST-3708 LOINC 98118-1 | This test identifies pathogenic variants in the SCNN1G gene associated with Liddle syndrome, a form of genetic hypertension. | Whole blood (EDTA), extracted genomic DNA, or dried blood spot on FTA card | 3–4 weeks | 2,800.00 AED | Details |
Clinical overview
About Inherited Disorders
Before your appointment
Preparation & sample collection
Follow the instructions you are given
Fasting, timing and medicine restrictions differ between investigations. The instructions for your specific request are confirmed when you book.
Bring your identification
A valid photo ID is required at collection so that your sample is matched correctly to your record.
Tell us about medicines
Prescription medicines, supplements and recent procedures can affect how an investigation is scheduled or interpreted — please mention them.
Ask before collection
If anything about preparation is unclear, contact us before your appointment. Preparation errors can affect reporting times.
Patient information
Frequently asked questions
Practical answers about Inherited Disorders testing at DNA Labs UAE. This information is general and does not replace advice from your treating clinician.
How do I choose the right Inherited Disorders test?
The correct investigation depends on what your clinician is trying to establish. Review the specimen type and turnaround time below, then confirm the choice with your treating doctor before booking.
What specimen is required?
Specimen requirements are listed for each investigation. If a request involves more than one sample type, our team will confirm what is needed at the time of booking.
Do you offer home sample collection in Dubai and the UAE?
Yes. Home collection can be arranged across Dubai and the wider UAE. Availability and appointment windows vary by location, so please confirm when you book.
How long do results take?
Turnaround depends on the investigation and the method used. The expected reporting time is confirmed with you before collection.
Is there anything I need to do before sample collection?
Some investigations require fasting, a specific collection time, or avoiding certain medicines or activities. Preparation details are shared when you book — please follow them and ask if anything is unclear.
How will I receive my report?
Reports are issued as secure digital documents and can be shared with your referring clinician on request. Please review results with a qualified clinician who can interpret them in context.
About this clinical information
The information on this Inherited Disorders page describes laboratory investigations in general terms. It is written to help you understand what an investigation involves — it is not a diagnosis and it is not a substitute for advice from your treating clinician.
- Investigation names, specimen types and listed prices are reviewed against laboratory records.
- Preparation guidance is indicative — confirm test-specific instructions before collection.
- Content is updated when investigations, methods or reporting formats change.
- Results are released to the patient and, on request, shared with the referring clinician.
Medical disclaimer: This page is for general information and education only. It is not medical advice, diagnosis or treatment, and it does not replace a consultation with a qualified healthcare professional. Always seek the advice of your doctor or another qualified provider with any questions about a medical condition or before ordering a test.
We're here to help
Need help choosing a Inherited Disorders test?
Tell us what your clinician has requested and we'll confirm availability, price, preparation and the most convenient collection option — including home collection in Dubai and across the UAE.
- Home collection available across the UAE
- Digital reports delivered securely
- Confidential handling of every request
Related areas