Coagulation Disorders tests in Dubai & UAE

Compare available Coagulation Disorders 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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1,400.00–3,000.00 AED

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Coagulation Disorders test prices

Showing 1–13 of 13 matching tests.

Coagulation Disorders diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-3403 Blood Coagulation Panel Genetic Test 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	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Genetic variants in 84 coagulation-related genes", "Presence of mutations causing inherited bleeding or clotting disorders"] Parameters [] Preparation ["No fasting required", "Pre-test genetic counseling session is mandatory (conducted via telemedicine)"] Indications ["Diagnosis of inherited bleeding disorders (e.g., haemophilia, von Willebrand disease)", "Diagnosis of inherited thrombophilia", "Family risk assessment for coagulation disorders", "Personalized treatment planning"] Measurement technique Confirm with laboratory Codes LOINC: 81305-8 ICD-10: D68.9 Clinical summary This test evaluates 84 genes for mutations associated with inherited bleeding, thrombotic, and platelet disorders.
TEST-3874 F13A1 Gene Factor XIIIA Deficiency Genetic Test 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	View
View test specifications and preparation Hide test specifications and preparation What it measures ["F13A1 gene sequence", "Pathogenic variants (point mutations, insertions/deletions, copy number variations)"] Parameters [] Preparation ["Mandatory genetic counselling session before specimen collection", "Provide full clinical history", "No fasting required unless other tests are bundled"] Indications ["Diagnosis of congenital Factor XIII deficiency", "Family planning for individuals with Factor XIII deficiency", "Confirmation of diagnosis in patients with bleeding disorders"] Measurement technique Confirm with laboratory Codes LOINC: 96737-3 ICD-10: D68.2 Clinical summary This genetic test analyzes the F13A1 gene for mutations associated with Factor XIII deficiency, a rare bleeding disorder.
TEST-6360 F2 Gene (Prothrombin) Factor II Deficiency NGS Test 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	View
View test specifications and preparation Hide test specifications and preparation What it measures ["F2 gene sequence", "Pathogenic variants in F2 gene", "G20210A mutation"] Parameters [] Preparation ["No fasting required", "Stay hydrated", "Inform phlebotomist of all medications, especially blood thinners"] Indications ["Diagnosis of congenital factor II deficiency", "Assessment of thrombophilic risk (G20210A mutation)", "Individuals with unexplained bleeding or bruising", "Family history of factor II deficiency"] Measurement technique Confirm with laboratory Codes LOINC: 98124-0 ICD-10: D68.2 Clinical summary This test evaluates the F2 gene for mutations associated with factor II deficiency (bleeding risk) and the G20210A mutation (thrombotic risk).
TEST-3261 F2 Prothrombin Gene Dysprothrombinemia Genetic Test 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	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Prothrombin G20210A mutation"] Parameters [] Preparation ["No fasting required", "Genetic counselling session recommended prior to sample collection"] Indications ["Assessment of inherited thrombophilia risk", "Guidance for anticoagulation therapy decisions", "Evaluation in individuals with unexplained VTE"] Measurement technique Confirm with laboratory Codes LOINC: 21644-6 ICD-10: D68.52 Clinical summary This genetic test identifies the presence of the prothrombin G20210A mutation, a common inherited risk factor for venous thromboembolism.
TEST-4009 F7 Gene Factor VII Deficiency Genetic Test 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	View
View test specifications and preparation Hide test specifications and preparation What it measures ["F7 gene coding regions", "F7 gene splice junctions"] Parameters [] Preparation ["Pre-test genetic counselling is mandatory", "Complete a detailed pedigree chart"] Indications ["Confirmation of suspected hereditary Factor VII deficiency", "Cascade screening of at-risk family members", "Risk stratification for surgery, pregnancy, and trauma"] Measurement technique Confirm with laboratory Codes LOINC: 92551-4 ICD-10: D68.2 Clinical summary This test identifies genetic variants in the F7 gene associated with hereditary Factor VII deficiency.
TEST-3122 F9 Gene Thrombophilia (X‑linked, Factor IX Defect) Genetic Test 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	View
View test specifications and preparation Hide test specifications and preparation What it measures ["F9 gene variants", "Gain-of-function mutations", "Single nucleotide variants", "Indels", "Copy number changes"] Parameters [] Preparation ["Fasting is not required", "Bring detailed three-generation family history", "Bring previous clotting test results", "Bring a list of current medications"] Indications ["Assessment of inherited thrombophilia risk", "Family screening for F9 gene variants", "Predictive testing in minors (with counselling and consent)", "Evaluation of unexplained VTE"] Measurement technique Confirm with laboratory Codes LOINC: 35071-4 ICD-10: D68.5 Clinical summary This genetic test evaluates the F9 gene for variants associated with X-linked thrombophilia, a condition increasing the risk of blood clots.
TEST-3253 Factor X Deficiency (F10 Gene) Genetic Test 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	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the F10 gene", "Single-nucleotide variants", "Small insertions/deletions", "Copy-number alterations"] Parameters [] Preparation ["No specific fasting required", "Continue all prescribed medications"] Indications ["Suspected hereditary factor X deficiency", "Indeterminate results from functional clotting assays", "Family history of factor X deficiency", "Carrier screening"] Measurement technique Confirm with laboratory Codes LOINC: 81306-3 ICD-10: D68.2, Z14.8, Z84.1 Clinical summary This test identifies pathogenic variants in the F10 gene associated with hereditary factor X deficiency.
TEST-3394 FGA Gene Congenital Afibrinogenemia Genetic Test This genetic test identifies mutations in the FGA gene responsible for congenital afibrinogenemia, a condition causing the complete absence of fibrinogen.	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 ["FGA gene pathogenic variants", "Fibrinogen absence"] Parameters [] Preparation [] Indications ["Suspected congenital afibrinogenemia", "Family history of afibrinogenemia", "Unexplained bleeding disorder"] Measurement technique Confirm with laboratory Codes LOINC: 82174-8 ICD-10: D68.2 Clinical summary This genetic test identifies mutations in the FGA gene responsible for congenital afibrinogenemia, a condition causing the complete absence of fibrinogen.
TEST-3355 FGB Gene Congenital Afibrinogenemia Genetic Test This test identifies pathogenic variants in the FGB gene responsible for congenital afibrinogenemia, a condition characterized by the absence of fibrinogen.	Whole Blood (EDTA), Extracted DNA, or FTA Card Blood Spot	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["FGB gene sequence", "Pathogenic variants"] Parameters [] Preparation ["No fasting required", "Continue routine medications unless advised otherwise by physician", "Mandatory pre-test genetic counselling session"] Indications ["Suspected congenital afibrinogenemia", "Family history of afibrinogenemia", "Inconclusive coagulation test results"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: D68.2 Clinical summary This test identifies pathogenic variants in the FGB gene responsible for congenital afibrinogenemia, a condition characterized by the absence of fibrinogen.
TEST-3390 FGG Gene Congenital Afibrinogenemia Genetic Test 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	View
View test specifications and preparation Hide test specifications and preparation What it measures ["FGG gene sequence", "Copy Number Variations (CNV) in FGG gene"] Parameters [] Preparation ["Inform phlebotomist of all medications, especially anticoagulants", "Sample submission requires clinical history and pedigree chart"] Indications ["Suspected congenital afibrinogenemia", "Family history of afibrinogenemia", "Evaluation of unexplained bleeding"] Measurement technique Confirm with laboratory Codes LOINC: 21641-2 ICD-10: D68.2 Clinical summary This test evaluates the FGG gene for mutations causing congenital afibrinogenemia.
TEST-3146 GGCX Gene Vitamin K‑Dependent Clotting Factors Combined Deficiency Type 1 Genetic Test This genetic test identifies pathogenic variants in the GGCX gene associated with hereditary combined deficiency of vitamin K-dependent clotting factors type 1.	Peripheral Whole Blood (EDTA or ACD tube)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["GGCX gene sequence", "Pathogenic variants (SNVs, indels, splice-site mutations)"] Parameters [] Preparation ["No fasting or dietary restrictions are needed", "Attend a mandatory pre-test genetic counselling session", "Bring records of prior bleeding episodes or family history"] Indications ["Suspected hereditary combined deficiency of vitamin K-dependent clotting factors type 1", "Family cascade screening for VKCFD1", "Guiding personalised haematology management"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: D68.8 Clinical summary This genetic test identifies pathogenic variants in the GGCX gene associated with hereditary combined deficiency of vitamin K-dependent clotting factors type 1.
TEST-1436 Hemophilia A Carrier Detection Test 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	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Factor VIII antigen levels", "Factor VIII activity (clotting function)", "Presence of F8 gene mutation (implied)"] Parameters [{"name": "Factor VIII Antigen", "reference_range": null}, {"name": "Factor VIII Activity", "reference_range": null}] Preparation ["Overnight fasting is preferred but not mandatory.", "Discontinue Heparin 1 day before the test if prescribed.", "Discontinue oral anticoagulants (warfarin, rivaroxaban) 7 days before the test if prescribed, with physician authorization.", "Complete a coagulation requisition form (Form 15)."] Indications ["Pre-conception screening for females with a family history of Hemophilia A", "Genetic counselling for families with Hemophilia A", "Evaluation of unexplained bleeding tendencies in females"] Measurement technique Confirm with laboratory Codes LOINC: 3209-5 ICD-10: Z14.01 Clinical summary This test evaluates a female's carrier status for Hemophilia A by assessing Factor VIII levels and function.
TEST-3972 PROS1 Gene Protein S Deficiency Genetic Test 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	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the PROS1 gene", "Inherited predisposition to Protein S deficiency"] Parameters [] Preparation ["No specific fasting required", "Inform lab if on anticoagulants or other medications"] Indications ["Evaluation of personal or family history of VTE", "Diagnosis of inherited thrombophilia", "Guiding thromboprophylaxis decisions"] Measurement technique Confirm with laboratory Codes LOINC: 82186-7 ICD-10: D68.59 Clinical summary This test identifies pathogenic variants within the PROS1 gene associated with inherited Protein S deficiency.

Category overview

Coagulation Disorders: overview

A family history of severe, unexplained bleeding episodes or recurrent, dangerous blood clots requires proactive molecular insights to protect your lifelong vascular health. Integrated into our comprehensive Genetics services, testing for genetic Coagulation Disorders maps your DNA for inherited mutations—such as those causing hemophilia or Factor V Leiden—that disrupt your body’s natural hemostatic balance. Utilizing advanced diagnostic technology, this highly targeted genomic screening uncovers the precise biological root of your symptoms, offering the critical clarity needed to safely guide highly personalized blood-thinning protocols, targeted factor replacement therapies, and specialized surgical preparations. Highly regarded for specialized blood diagnostics among the best diagnostic labs in the UAE, DNA Labs guarantees absolute patient confidentiality, exceptional analytical precision, and remarkably fast reporting. Safeguard your cardiovascular future—schedule your coagulation disorders genetic testing in UAE, coordinate a seamless home sample collection, or consult our dedicated hematology genetics team.

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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.