Cardiomyopathy Genetic tests in Dubai & UAE

Compare available Cardiomyopathy Genetic 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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1,100.00–2,800.00 AED

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Cardiomyopathy Genetic test prices

Showing 1–15 of 40 matching tests.

Cardiomyopathy Genetic diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4309 ABCC9 Gene Dilated Cardiomyopathy Type 1O Genetic Test UAE This genetic test identifies pathogenic variants in the ABCC9 gene associated with dilated cardiomyopathy type 1O.	Whole blood (peripheral)	3 – 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in ABCC9 gene", "Variants of Uncertain Significance (VUS) in ABCC9 gene"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any relevant medications"] Indications ["Diagnosis of dilated cardiomyopathy type 1O", "Carrier screening for ABCC9-related cardiomyopathy", "Risk stratification for family members"] Measurement technique Confirm with laboratory Codes LOINC: 81326-5 ICD-10: I42.0 Clinical summary This genetic test identifies pathogenic variants in the ABCC9 gene associated with dilated cardiomyopathy type 1O.
TEST-4306 ACTC1 Gene Cardiomyopathy (Dilated Type 1R) Genetic Test This genetic test identifies pathogenic variants in the ACTC1 gene associated with dilated cardiomyopathy type 1R.	Whole Blood (Peripheral)	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 ACTC1 gene"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Personal or family history of unexplained dilated cardiomyopathy", "Young-onset heart failure", "Sudden cardiac death", "Risk stratification for athletes"] Measurement technique Confirm with laboratory Codes LOINC: 85145-6 ICD-10: I42.0 Clinical summary This genetic test identifies pathogenic variants in the ACTC1 gene associated with dilated cardiomyopathy type 1R.
TEST-4264 CALR3 Gene Familial Hypertrophic Cardiomyopathy Type 19 Genetic Test This test identifies pathogenic variants in the CALR3 gene associated with Familial Hypertrophic Cardiomyopathy Type 19.	Peripheral Whole Blood (EDTA), Extracted DNA, or FTA Card Spot	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 CALR3 gene", "Deletion/duplication analysis of the CALR3 gene"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medications without consulting your cardiologist"] Indications ["Individuals with a family history of hypertrophic cardiomyopathy", "Individuals experiencing symptoms suggestive of hypertrophic cardiomyopathy", "Cascade screening for at-risk relatives"] Measurement technique Confirm with laboratory Codes LOINC: 93680-8 ICD-10: I42.1, I42.8, Z15.89 Clinical summary This test identifies pathogenic variants in the CALR3 gene associated with Familial Hypertrophic Cardiomyopathy Type 19.
TEST-4301 CAV3 Gene Familial Hypertrophic Cardiomyopathy (HCM) Genetic Test This genetic test evaluates the CAV3 gene for pathogenic variants linked to familial hypertrophic cardiomyopathy.	Peripheral whole blood (EDTA) or buccal swab	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 CAV3 gene", "Copy Number Variations (CNVs) within the CAV3 gene"] Parameters [] Preparation ["No specific fasting required", "No medication or diet changes needed prior to sample collection"] Indications ["Personal or family history suggestive of hypertrophic cardiomyopathy", "Need for confirmatory genetic analysis", "Pre-participation cardiac screening for athletes", "First-degree relatives of a known CAV3 variant carrier"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: I42.1 Clinical summary This genetic test evaluates the CAV3 gene for pathogenic variants linked to familial hypertrophic cardiomyopathy.
TEST-4352 CRYAB Gene Cardiomyopathy, Dilated Type 1 Genetic Test This genetic test evaluates the CRYAB gene for pathogenic variants associated with dilated cardiomyopathy type 1.	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 ["Pathogenic variants in the CRYAB gene"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Diagnosis of inherited dilated cardiomyopathy type 1", "Family screening for CRYAB mutations", "Risk assessment in individuals with family history"] Measurement technique Confirm with laboratory Codes LOINC: 80505-2 ICD-10: I42.0 Clinical summary This genetic test evaluates the CRYAB gene for pathogenic variants associated with dilated cardiomyopathy type 1.
TEST-4313 CSRP3 Gene Dilated Cardiomyopathy Type 1M Genetic Test This genetic test identifies pathogenic variants in the CSRP3 gene associated with dilated cardiomyopathy type 1M.	Whole blood (EDTA), FTA card, or extracted 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 the CSRP3 gene", "Coding exons and splice sites"] Parameters [] Preparation ["Genetic counselling session required before sample collection", "Informed consent required"] Indications ["Diagnosis of dilated cardiomyopathy type 1M", "Familial cascade testing for CSRP3 mutations", "Risk assessment in individuals with family history"] Measurement technique Confirm with laboratory Codes LOINC: 21685-1 ICD-10: I42.0 Clinical summary This genetic test identifies pathogenic variants in the CSRP3 gene associated with dilated cardiomyopathy type 1M.
TEST-4293 CSRP3 Gene Familial Hypertrophic Cardiomyopathy Type 12 Genetic Test This test identifies pathogenic variants in the CSRP3 gene associated with Familial Hypertrophic Cardiomyopathy Type 12.	Peripheral whole blood (3–5 mL EDTA tube) or FTA card dried blood spot	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 CSRP3 gene", "Coding regions and splice sites of the CSRP3 gene"] Parameters [] Preparation ["No fasting required", "No special preparation required"] Indications ["Individuals with a family history of hypertrophic cardiomyopathy", "Individuals with clinical features suggestive of hypertrophic cardiomyopathy", "Cascade testing for family members of an individual with a known CSRP3 pathogenic variant"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: I42.2 Clinical summary This test identifies pathogenic variants in the CSRP3 gene associated with Familial Hypertrophic Cardiomyopathy Type 12.
TEST-4348 DES Gene Dilated Cardiomyopathy Type 1I Genetic Test This genetic test evaluates the entire DES gene for variants associated with dilated cardiomyopathy type 1I.	Peripheral Blood (EDTA or ACD tubes) or Extracted DNA	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic and likely pathogenic variants in the DES gene", "Coding exons, intronic boundaries, and regulatory regions"] Parameters [] Preparation ["No specific fasting required", "No medication or diet restrictions"] Indications ["Diagnosis of dilated cardiomyopathy type 1I", "Family screening for DES gene mutations", "Risk assessment in individuals with cardiac symptoms"] Measurement technique Confirm with laboratory Codes LOINC: 82326-8 ICD-10: I42.0 Clinical summary This genetic test evaluates the entire DES gene for variants associated with dilated cardiomyopathy type 1I.
TEST-4463 DSG2 Gene (Arrhythmogenic Right Ventricular Cardiomyopathy Type 10) Genetic Test This test identifies pathogenic variants in the DSG2 gene associated with Arrhythmogenic Right Ventricular Cardiomyopathy Type 10 (ARVC10).	Peripheral whole blood (EDTA tube)	3–4 weeks (expedited reporting available on request)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the DSG2 gene", "Single-nucleotide variants", "Small insertions and deletions", "Copy-number alterations"] Parameters [] Preparation ["No specific fasting required", "No special medication or diet restrictions"] Indications ["Confirmed clinical diagnosis of ARVC", "Unexplained right ventricular structural abnormalities", "Family history of ARVC", "First- or second-degree relative with sudden cardiac death before age 50", "Sports eligibility assessment", "ICD implantation planning", "Family cascade screening"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: I42.8 Clinical summary This test identifies pathogenic variants in the DSG2 gene associated with Arrhythmogenic Right Ventricular Cardiomyopathy Type 10 (ARVC10).
TEST-4455 DSP Gene Arrhythmogenic Right Ventricular Cardiomyopathy Type 8 (ARVC8) Genetic Test This genetic test identifies mutations in the DSP gene, which are associated with Arrhythmogenic Right Ventricular Cardiomyopathy Type 8 (ARVC8).	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 ["DSP gene mutations", "Presence of pathogenic variants"] Parameters [] Preparation ["Mandatory pre-test genetic counseling session"] Indications ["Family cascade screening for ARVC8", "Athletic clearance under UAE cardiac guidelines", "Pre-symptomatic detection in at-risk family members"] Measurement technique Confirm with laboratory Codes LOINC: 83890-4 ICD-10: I42.8 Clinical summary This genetic test identifies mutations in the DSP gene, which are associated with Arrhythmogenic Right Ventricular Cardiomyopathy Type 8 (ARVC8).
TEST-4324 EYA4 Gene Dilated Cardiomyopathy (Type 1J) Genetic Test This test identifies pathogenic variants in the EYA4 gene associated with dilated cardiomyopathy type 1J.	Peripheral Whole Blood (EDTA tube); DNA extraction from blood; alternative FTA card acceptable	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 EYA4 gene", "Deletion/duplication analysis (CNV) of the EYA4 gene"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue cardiac medications without physician consultation"] Indications ["Individuals with a strong family history of dilated cardiomyopathy", "Unexplained heart failure diagnosed before age 50", "Personal or family history of sudden cardiac death", "First-degree relatives of a confirmed EYA4 variant carrier"] Measurement technique Confirm with laboratory Codes LOINC: 94827-1 ICD-10: I42.0 Clinical summary This test identifies pathogenic variants in the EYA4 gene associated with dilated cardiomyopathy type 1J.
TEST-4292 FKTN Gene Cardiomyopathy, Dilated Type 1X Genetic Test This test detects pathogenic variants in the FKTN gene associated with dilated cardiomyopathy.	Peripheral Whole Blood	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 FKTN gene"] Parameters [] Preparation [] Indications ["Diagnosis of dilated cardiomyopathy", "Family screening for FKTN-related cardiomyopathy", "Risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 81330-4 ICD-10: I42.0 Clinical summary This test detects pathogenic variants in the FKTN gene associated with dilated cardiomyopathy.
TEST-4287 GATAD1 Gene Dilated Cardiomyopathy Type 2B Genetic Test This test identifies pathogenic variants in the GATAD1 gene associated with autosomal recessive dilated cardiomyopathy.	Whole Blood (Peripheral Blood)	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 GATAD1 gene"] Parameters [] Preparation ["No fasting required", "Complete a genetic counselling session prior to draw", "Inform phlebotomist of any anticoagulant therapy"] Indications ["Diagnosis of autosomal recessive dilated cardiomyopathy", "Family risk assessment for dilated cardiomyopathy", "Cascade testing in families with known GATAD1 mutations"] Measurement technique Confirm with laboratory Codes LOINC: 47901-1 ICD-10: I42.0 Clinical summary This test identifies pathogenic variants in the GATAD1 gene associated with autosomal recessive dilated cardiomyopathy.
TEST-4290 JPH2 Gene Cardiomyopathy (Familial Hypertrophic Type 17) Genetic Test This genetic test identifies pathogenic variants in the JPH2 gene associated with familial hypertrophic cardiomyopathy type 17.	Whole Blood (Peripheral)	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 JPH2 gene"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of all medications"] Indications ["Family history of hypertrophic cardiomyopathy", "Known JPH2 variant in a relative", "Unexplained heart muscle thickening"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: I42.2 Clinical summary This genetic test identifies pathogenic variants in the JPH2 gene associated with familial hypertrophic cardiomyopathy type 17.
TEST-3986 LDB3 Gene Cardiomyopathy, Hypertrophic, Type 24 Genetic Test This test identifies pathogenic variants in the LDB3 gene associated with hypertrophic cardiomyopathy type 24 and related neurological disorders.	Peripheral Blood or FTA Card (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 the LDB3 gene"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any recent bone marrow transplant"] Indications ["Diagnosis of hypertrophic cardiomyopathy type 24", "Risk assessment for family members", "Pre-symptomatic testing"] Measurement technique Confirm with laboratory Codes LOINC: 21607-6 ICD-10: I42.1 Clinical summary This test identifies pathogenic variants in the LDB3 gene associated with hypertrophic cardiomyopathy type 24 and related neurological disorders.

Category overview

Cardiomyopathy Genetic: overview

Navigating unexplained heart failure or an enlarged heart requires highly specific diagnostic clarity to unlock the most effective, personalized cardiac care. As an advanced offering in our Genetics department, Cardiomyopathy Genetic testing meticulously maps your DNA to identify specific inherited mutations that weaken the heart muscle, such as those causing hypertrophic or dilated cardiomyopathy. By leveraging cutting-edge genomic technology, this crucial preventative screening helps confirm your diagnosis and assess familial risks, providing the definitive data needed to safely guide life-saving cardiovascular management and targeted therapies. Consistently trusted by cardiologists across premier diagnostic labs in Dubai and the UAE, DNA Labs ensures strict patient confidentiality, unparalleled diagnostic accuracy, and prompt, reliable turnaround times. Protect your cardiovascular wellness—book your cardiomyopathy genetic testing in UAE, arrange a secure home sample collection, or consult our expert medical professionals.

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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.