Genetics
Coagulation 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
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Coagulation Disorders investigations
All 13 investigations in this category are listed below.
| Test | What it measures | Specimen | Turnaround | Price | Book |
|---|---|---|---|---|---|
| Blood Coagulation Panel Genetic Test TEST-3403 LOINC 81305-8 | This test evaluates 84 genes for mutations associated with inherited bleeding, thrombotic, and platelet disorders. | Peripheral whole blood | 3–4 weeks from sample receipt | 3,000.00 AED | Details |
| F13A1 Gene Factor XIIIA Deficiency Genetic Test TEST-3874 LOINC 96737-3 | This genetic test analyzes the F13A1 gene for mutations associated with Factor XIII deficiency, a rare bleeding disorder. | Peripheral Whole Blood (preferred), extracted DNA, or FTA card | 3 – 4 weeks | 2,800.00 AED | Details |
| F2 Gene (Prothrombin) Factor II Deficiency NGS Test TEST-6360 LOINC 98124-0 | This test evaluates the F2 gene for mutations associated with factor II deficiency (bleeding risk) and the G20210A mutation (thrombotic risk). | Peripheral Blood (EDTA), Extracted DNA, or Dried Blood Spot (FTA Card) | 3 to 4 Weeks | 2,800.00 AED | Details |
| F2 Prothrombin Gene Dysprothrombinemia Genetic Test TEST-3261 LOINC 21644-6 | This genetic test identifies the presence of the prothrombin G20210A mutation, a common inherited risk factor for venous thromboembolism. | Peripheral venous whole blood (EDTA tube) | 3–4 Weeks | 2,800.00 AED | Details |
| F7 Gene Factor VII Deficiency Genetic Test TEST-4009 LOINC 92551-4 | This test identifies genetic variants in the F7 gene associated with hereditary Factor VII deficiency. | Whole Blood (EDTA) | 3 – 4 Weeks | 2,800.00 AED | Details |
| F9 Gene Thrombophilia (X‑linked, Factor IX Defect) Genetic Test TEST-3122 LOINC 35071-4 | This genetic test evaluates the F9 gene for variants associated with X-linked thrombophilia, a condition increasing the risk of blood clots. | Peripheral Whole Blood | 3–4 weeks | 2,800.00 AED | Details |
| Factor X Deficiency (F10 Gene) Genetic Test TEST-3253 LOINC 81306-3 | This test identifies pathogenic variants in the F10 gene associated with hereditary factor X deficiency. | Peripheral whole blood | 3–4 weeks | 2,800.00 AED | Details |
| FGA Gene Congenital Afibrinogenemia Genetic Test TEST-3394 LOINC 82174-8 | This genetic test identifies mutations in the FGA gene responsible for congenital afibrinogenemia, a condition causing the complete absence of fibrino... | Peripheral whole blood (EDTA) | 3–4 weeks | 2,800.00 AED | Details |
| FGB Gene Congenital Afibrinogenemia Genetic Test TEST-3355 LOINC 21636-6 | This test identifies pathogenic variants in the FGB gene responsible for congenital afibrinogenemia, a condition characterized by the absence of fibri... | Whole Blood (EDTA), Extracted DNA, or FTA Card Blood Spot | 3–4 weeks | 2,800.00 AED | Details |
| FGG Gene Congenital Afibrinogenemia Genetic Test TEST-3390 LOINC 21641-2 | This test evaluates the FGG gene for mutations causing congenital afibrinogenemia. | Peripheral Whole Blood / Extracted DNA / FTA Card | 3–4 Weeks | 2,800.00 AED | Details |
| GGCX Gene Vitamin K‑Dependent Clotting Factors Combined Deficiency Type 1 Genetic Test TEST-3146 LOINC 81247-9 | This genetic test identifies pathogenic variants in the GGCX gene associated with hereditary combined deficiency of vitamin K-dependent clotting facto... | Peripheral Whole Blood (EDTA or ACD tube) | 3–4 Weeks | 2,800.00 AED | Details |
| Hemophilia A Carrier Detection Test TEST-1436 LOINC 3209-5 | This test evaluates a female's carrier status for Hemophilia A by assessing Factor VIII levels and function. | 3 mL whole blood in 3.2% sodium citrate (blue top) | Next day (sample received Mon–Wed by 11 AM; report delivered following working day) | 1,400.00 AED | Details |
| PROS1 Gene Protein S Deficiency Genetic Test TEST-3972 LOINC 82186-7 | This test identifies pathogenic variants within the PROS1 gene associated with inherited Protein S deficiency. | Peripheral Whole Blood (EDTA) | 3 to 4 Weeks | 2,800.00 AED | Details |
Clinical overview
About Coagulation 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 Coagulation 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 Coagulation 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 Coagulation 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.
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Need help choosing a Coagulation 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
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