Genetics
Cardiomyopathy Genetic 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.
3 min read
- Quality-controlled laboratory
- Home collection across the UAE
- Confidential handling of results
Compare options
Cardiomyopathy Genetic investigations
All 40 investigations in this category are listed below.
| Test | What it measures | Specimen | Turnaround | Price | Book |
|---|---|---|---|---|---|
| ABCC9 Gene Dilated Cardiomyopathy Type 1O Genetic Test UAE TEST-4309 LOINC 81326-5 | 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 | Details |
| ACTC1 Gene Cardiomyopathy (Dilated Type 1R) Genetic Test TEST-4306 LOINC 85145-6 | 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 | Details |
| CALR3 Gene Familial Hypertrophic Cardiomyopathy Type 19 Genetic Test TEST-4264 LOINC 93680-8 | 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 | Details |
| CAV3 Gene Familial Hypertrophic Cardiomyopathy (HCM) Genetic Test TEST-4301 LOINC 21636-6 | 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 | Details |
| CRYAB Gene Cardiomyopathy, Dilated Type 1 Genetic Test TEST-4352 LOINC 80505-2 | 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 | Details |
| CSRP3 Gene Dilated Cardiomyopathy Type 1M Genetic Test TEST-4313 LOINC 21685-1 | 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 | Details |
| CSRP3 Gene Familial Hypertrophic Cardiomyopathy Type 12 Genetic Test TEST-4293 LOINC 21636-6 | 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 | Details |
| DES Gene Dilated Cardiomyopathy Type 1I Genetic Test TEST-4348 LOINC 82326-8 | 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 | Details |
| DSG2 Gene (Arrhythmogenic Right Ventricular Cardiomyopathy Type 10) Genetic Test TEST-4463 LOINC 21636-6 | 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 | Details |
| DSP Gene Arrhythmogenic Right Ventricular Cardiomyopathy Type 8 (ARVC8) Genetic Test TEST-4455 LOINC 83890-4 | 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 | Details |
| EYA4 Gene Dilated Cardiomyopathy (Type 1J) Genetic Test TEST-4324 LOINC 94827-1 | 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 | Details |
| FKTN Gene Cardiomyopathy, Dilated Type 1X Genetic Test TEST-4292 LOINC 81330-4 | This test detects pathogenic variants in the FKTN gene associated with dilated cardiomyopathy. | Peripheral Whole Blood | 3 to 4 Weeks | 2,800.00 AED | Details |
| GATAD1 Gene Dilated Cardiomyopathy Type 2B Genetic Test TEST-4287 LOINC 47901-1 | 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 | Details |
| JPH2 Gene Cardiomyopathy (Familial Hypertrophic Type 17) Genetic Test TEST-4290 LOINC 21636-6 | 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 | Details |
| LDB3 Gene Cardiomyopathy, Hypertrophic, Type 24 Genetic Test TEST-3986 LOINC 21607-6 | 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 | Details |
| LDB3 Gene-Related Dilated Cardiomyopathy Type 1C (DCM-1C) Genetic Test TEST-4345 LOINC 21636-6 | This genetic test evaluates for pathogenic variants in the LDB3 gene associated with autosomal dominant dilated cardiomyopathy type 1C. | Whole Blood (EDTA), Extracted DNA, or FTA Card | 3–4 Weeks | 2,800.00 AED | Details |
| Maternally Inherited Cardiomyopathy (MICM) Mutation Detection Test TEST-2542 LOINC 83092-7 | This test detects pathogenic variants within the entire mitochondrial DNA sequence associated with maternally inherited cardiomyopathy. | EDTA whole blood (peripheral) | 10 working days from sample receipt | 1,100.00 AED | Details |
| MT-TH Gene Sequencing for Idiopathic Dilated Mitochondrial Cardiomyopathy (NGS) Test TEST-4262 LOINC 94390-5 | This test identifies pathogenic variants in the MT-TH gene, which can cause mitochondrial dilated cardiomyopathy. | Whole blood (EDTA), FTA card, or extracted DNA | 3 to 4 Weeks | 2,800.00 AED | Details |
| MT-TI Gene Cardiomyopathy‑Related Genetic Test TEST-4271 LOINC 68748-5 | This genetic test identifies pathogenic variants in the mitochondrial MT-TI gene associated with maternally inherited cardiomyopathy. | Whole blood (EDTA), extracted DNA, or FTA card | 3–4 weeks | 2,800.00 AED | Details |
| MT‑TG Gene Hypertrophic Cardiomyopathy (MT‑TG‑Related) Genetic Test TEST-4266 LOINC 100376-2 | This test identifies pathogenic variants in the MT‑TG gene linked to hypertrophic cardiomyopathy. | Peripheral Whole Blood (EDTA) or Dried Blood Spot (DBS) | 3–4 weeks | 2,800.00 AED | Details |
| MYBPC3 Gene Cardiomyopathy, Familial Hypertrophic Type 4 Genetic Test TEST-4283 LOINC 21636-6 | This test identifies pathogenic variants in the MYBPC3 gene, a common cause of familial hypertrophic cardiomyopathy. | Whole Blood (Peripheral) – EDTA tube | 3 to 4 Weeks | 2,800.00 AED | Details |
| MYH7 Gene Cardiomyopathy (Dilated Type 1S) Genetic Test TEST-4331 LOINC 81324-7 | This genetic test evaluates the MYH7 gene for pathogenic variants linked to dilated cardiomyopathy type 1S. | Peripheral whole blood | 3–4 Weeks | 2,800.00 AED | Details |
| MYH7 Gene Cardiomyopathy, Familial Hypertrophic Type 1 Genetic Test TEST-4275 LOINC 94246-7 | This test identifies pathogenic variants within the MYH7 gene associated with familial hypertrophic cardiomyopathy type 1. | Whole Blood (Peripheral) | 3 to 4 weeks | 2,800.00 AED | Details |
| MYL2 Gene Familial Hypertrophic Cardiomyopathy Type 10 Genetic Test TEST-4297 LOINC 93172-3 | This test identifies pathogenic variants in the MYL2 gene associated with familial hypertrophic cardiomyopathy type 10. | Peripheral whole blood (3–5 mL in EDTA tube), extracted DNA, or dried blood spot (FTA card) | 3–4 weeks | 2,800.00 AED | Details |
| MYL3 Gene (Familial Hypertrophic Cardiomyopathy Type 8) Test TEST-4251 LOINC 104207-1 | This genetic test identifies pathogenic variants within the MYL3 gene, which are associated with familial hypertrophic cardiomyopathy type 8. | Whole Blood (EDTA), Extracted DNA, or DNA FTA Card | 3–4 weeks | 2,800.00 AED | Details |
| MYOZ2 Gene (Familial Hypertrophic Cardiomyopathy Type 16) Genetic Test TEST-4268 LOINC 93929-0 | This test evaluates the MYOZ2 gene for variants associated with familial hypertrophic cardiomyopathy type 16. | Peripheral whole blood | 3–4 weeks | 2,800.00 AED | Details |
| MYPN Gene Dilated Cardiomyopathy Type 1KK Genetic Test TEST-4343 LOINC 101943-6 | This test analyzes the MYPN gene for pathogenic variants associated with Dilated Cardiomyopathy Type 1KK. | Peripheral Whole Blood or Buccal Swab | 3–4 Weeks | 2,800.00 AED | Details |
| PRKAG2 Gene Cardiomyopathy, Familial Hypertrophic Type 6 Genetic Test TEST-4256 LOINC 55233-1 | This genetic test detects mutations in the PRKAG2 gene linked to familial hypertrophic cardiomyopathy type 6. | Peripheral Whole Blood | 3–4 Weeks | 2,800.00 AED | Details |
| SCN5A Gene Dilated Cardiomyopathy Type 1E Genetic Test TEST-4336 LOINC 21636-6 | This genetic test identifies pathogenic variants in the SCN5A gene associated with Dilated Cardiomyopathy Type 1E. | Peripheral Whole Blood (collected in EDTA tube) | 3 to 4 weeks | 2,800.00 AED | Details |
| SGCD Gene Dilated Cardiomyopathy (Type 1L) Genetic Test TEST-4319 LOINC 81301-7 | This test identifies pathogenic variants in the SGCD gene associated with dilated cardiomyopathy type 1L. | Peripheral whole blood (or extracted DNA/FTA card) | 3–4 weeks | 2,800.00 AED | Details |
| TCAP Gene Cardiomyopathy, Dilated Type 1N Genetic Test TEST-4337 LOINC 51958-7 | This genetic test identifies pathogenic variants in the TCAP gene associated with Dilated Cardiomyopathy Type 1N. | Peripheral whole blood (2 mL EDTA) or saliva (Oragene kit) | 3–4 weeks | 2,800.00 AED | Details |
| TMEM43 Gene Arrhythmogenic Right Ventricular Cardiomyopathy Type 5 Genetic Test TEST-4435 LOINC 90553-2 | This test identifies genetic variants in the TMEM43 gene associated with Arrhythmogenic Right Ventricular Cardiomyopathy Type 5 (ARVC5). | Peripheral whole blood (3–5 mL collected in EDTA tube) | 3–4 weeks (21–28 calendar days) from sample receipt | 2,800.00 AED | Details |
| TMPO Gene Dilated Cardiomyopathy Type 1T (Genetic Test) TEST-4303 LOINC 82186-6 | This genetic test identifies pathogenic mutations in the TMPO gene associated with familial dilated cardiomyopathy type 1T. | Whole Blood (EDTA), Extracted DNA, or Dried Blood Spot (FTA Card) | 3 to 4 Weeks | 2,800.00 AED | Details |
| TNNC1 Gene Cardiomyopathy Dilated Type 1Z Genetic Test TEST-4289 LOINC 21636-6 | This test evaluates the TNNC1 gene for pathogenic variants associated with dilated cardiomyopathy type 1Z. | Peripheral whole blood, extracted DNA, or dried blood spot (FTA card) | 3–4 Weeks | 2,800.00 AED | Details |
| TNNI3 Gene Cardiomyopathy, Dilated Type 2A Genetic Test TEST-4316 LOINC 94037-7 | This test evaluates the TNNI3 gene for pathogenic variants associated with autosomal dominant dilated cardiomyopathy type 2A. | Peripheral Whole Blood (EDTA) | 3–4 Weeks | 2,800.00 AED | Details |
| TNNT2 Gene Cardiomyopathy (Familial Hypertrophic Type 2) Genetic Test TEST-4286 LOINC 83290-0 | This test evaluates the TNNT2 gene for pathogenic variants associated with familial hypertrophic cardiomyopathy type 2. | Peripheral Whole Blood | 3–4 Weeks | 2,800.00 AED | Details |
| TNNT2 Gene Cardiomyopathy, Dilated Type 1D Genetic Test TEST-4341 LOINC 81326-5 | This test evaluates the TNNT2 gene for mutations associated with dilated cardiomyopathy type 1D. | Whole Blood (EDTA), Extracted DNA, FTA Card | 3–4 Weeks | 2,800.00 AED | Details |
| TPM1 Gene Cardiomyopathy, Dilated Type 1Y Genetic Test TEST-4320 LOINC 21636-6 | This test identifies pathogenic mutations within the TPM1 gene, a known cause of dilated cardiomyopathy type 1Y. | Peripheral whole blood (EDTA tube) | 3–4 weeks (from sample receipt) | 2,800.00 AED | Details |
| TTN Gene Cardiomyopathy, Dilated Type 1G (Genetic Test) TEST-4332 LOINC 82887-6 | This genetic test detects pathogenic variants in the TTN gene, a common cause of dilated cardiomyopathy. | Peripheral Whole Blood | 3–4 Weeks | 2,800.00 AED | Details |
| TTN Gene Cardiomyopathy, Familial Hypertrophic Type 9 Genetic Test TEST-4274 LOINC 92814-2 | This genetic test identifies pathogenic variants in the TTN gene associated with familial hypertrophic cardiomyopathy type 9. | Peripheral Whole Blood | 3–4 Weeks | 2,800.00 AED | Details |
Clinical overview
About Cardiomyopathy Genetic
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.
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 Cardiomyopathy Genetic testing at DNA Labs UAE. This information is general and does not replace advice from your treating clinician.
How do I choose the right Cardiomyopathy Genetic 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 Cardiomyopathy Genetic 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 Cardiomyopathy Genetic 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