Cardiomyopathy Genetics tests in Dubai & UAE

Compare available Cardiomyopathy Genetics 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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Listed price range

2,800.00 AED

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Cardiomyopathy Genetics test prices

Showing 1–7 of 7 matching tests.

Cardiomyopathy Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4355 MT-ATP8 Gene Genetic Test for Cardiomyopathy, Apical Hypertrophic Cardiomyopathy & Neuropathy This test sequences the MT-ATP8 gene to identify variants associated with specific types of cardiomyopathy and neuropathy.	Whole blood (EDTA), 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 ["MT-ATP8 gene variants", "Pathogenic mutations"] Parameters [] Preparation ["Submit detailed clinical history", "Mandatory genetic counselling session"] Indications ["Diagnosis of hereditary cardiomyopathies", "Diagnosis of apical hypertrophic cardiomyopathy", "Diagnosis of neuropathy associated with MT-ATP8 mutations", "Genetic counseling for affected families"] Measurement technique Confirm with laboratory Codes LOINC: 81258-9 ICD-10: I42.2, G60.9 Clinical summary This test sequences the MT-ATP8 gene to identify variants associated with specific types of cardiomyopathy and neuropathy.
TEST-4373 MYBPC3 Gene Dilated Cardiomyopathy Genetic Test This test identifies pathogenic or likely pathogenic variants in the MYBPC3 gene, a common cause of familial dilated cardiomyopathy.	Peripheral Whole Blood (EDTA), FTA Card, Extracted Genomic DNA	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["MYBPC3 gene variants", "Pathogenic mutations"] Parameters [] Preparation [] Indications ["Diagnosis of familial dilated cardiomyopathy", "Risk assessment in family members", "Guiding treatment decisions"] Measurement technique Confirm with laboratory Codes LOINC: 93215-9 ICD-10: I42.0 Clinical summary This test identifies pathogenic or likely pathogenic variants in the MYBPC3 gene, a common cause of familial dilated cardiomyopathy.
TEST-4258 MYH7B Gene Cardiomyopathy (Left Ventricular Noncompaction) Genetic Test This genetic test analyzes the MYH7B gene for pathogenic variants associated with Left Ventricular Noncompaction Cardiomyopathy (LVNC). It identifies mutations that may increase th...	Peripheral whole blood (EDTA) or FTA card	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 MYH7B gene", "Copy Number Variations (CNV) within the MYH7B gene"] Parameters [] Preparation ["No specific fasting required", "No need to stop prescribed cardiac medications"] Indications ["Individuals with clinical suspicion of LVNC", "Family members of individuals diagnosed with MYH7B-related LVNC", "Risk assessment for individuals with unexplained cardiomyopathy"] Measurement technique Confirm with laboratory Codes LOINC: 98551-3 ICD-10: I42.8, Z15.89 Clinical summary This genetic test analyzes the MYH7B gene for pathogenic variants associated with Left Ventricular Noncompaction Cardiomyopathy (LVNC). It identifies mutations that may increase the risk of developing this specific type of cardiomyopathy.
TEST-4335 PLN Gene Dilated Cardiomyopathy Type 1P (DCM1P) Genetic Test This test evaluates the PLN gene for pathogenic variants associated with Dilated Cardiomyopathy Type 1P (DCM1P).	Whole Blood, Extracted DNA, or FTA Card Blood Spot	21–28 Business Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PLN gene sequence", "Pathogenic variants in PLN gene"] Parameters [] Preparation ["No specific fasting required", "No medication adjustments needed"] Indications ["Diagnosis of Dilated Cardiomyopathy Type 1P (DCM1P)", "Family cascade screening for DCM1P", "Risk assessment for sudden cardiac death"] Measurement technique Confirm with laboratory Codes LOINC: 81301-1 ICD-10: I42.0 Clinical summary This test evaluates the PLN gene for pathogenic variants associated with Dilated Cardiomyopathy Type 1P (DCM1P).
TEST-4245 TNNI3 Gene (Familial Restrictive Cardiomyopathy Type 1) Genetic Test This test analyzes the TNNI3 gene for pathogenic variants associated with autosomal dominant familial restrictive cardiomyopathy type 1.	Whole Blood / FTA Card / 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 TNNI3 gene", "Large deletions or duplications in the TNNI3 gene"] Parameters [] Preparation [] Indications ["Diagnosis of familial restrictive cardiomyopathy type 1", "Cascade family screening for TNNI3 mutations", "Risk stratification in individuals with a family history"] Measurement technique Confirm with laboratory Codes LOINC: 78920-1 ICD-10: I42.5 Clinical summary This test analyzes the TNNI3 gene for pathogenic variants associated with autosomal dominant familial restrictive cardiomyopathy type 1.
TEST-4260 TPM1 Gene Sequencing for Familial Hypertrophic Cardiomyopathy Type 3 (NGS) Test This diagnostic test evaluates the entire TPM1 gene for pathogenic variants associated with familial hypertrophic cardiomyopathy type 3.	Peripheral Whole Blood (FTA Card acceptable)	15 – 20 Business Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the TPM1 gene", "Mutations affecting the tropomyosin protein"] Parameters [] Preparation ["Avoid strenuous exercise for 24 hours", "Stay hydrated", "No fasting required"] Indications ["Diagnosis of familial hypertrophic cardiomyopathy type 3", "Risk assessment for family members", "Guiding personalized cardiac management"] Measurement technique Confirm with laboratory Codes LOINC: 94212-9 ICD-10: I42.1, I42.2 Clinical summary This diagnostic test evaluates the entire TPM1 gene for pathogenic variants associated with familial hypertrophic cardiomyopathy type 3.
TEST-4323 VCL Gene Dilated Cardiomyopathy Type 1W Next-Generation Sequencing (NGS) Genetic Test This test evaluates the VCL gene for pathogenic variants associated with dilated cardiomyopathy type 1W.	Whole Blood, Extracted DNA, or FTA Card (Dried 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 VCL gene", "Copy number variants (CNVs) in the VCL gene"] Parameters [] Preparation ["Clinical genetic counselling session prior to sample collection", "Detailed family pedigree documentation"] Indications ["Diagnosis of dilated cardiomyopathy type 1W", "Genetic risk assessment for cardiomyopathy", "Family screening for VCL-related cardiomyopathy"] Measurement technique Confirm with laboratory Codes LOINC: 93239-3 ICD-10: I42.0 Clinical summary This test evaluates the VCL gene for pathogenic variants associated with dilated cardiomyopathy type 1W.

Category overview

Cardiomyopathy Genetics: overview

Understanding the broader hereditary factors affecting your heart's structural integrity empowers your family to make proactive, highly informed health decisions. Integrated into our elite Molecular Genetics services, comprehensive Cardiomyopathy Genetics screening provides an in-depth evaluation of the complex genetic pathways responsible for inherited heart muscle disorders. Utilizing advanced sequencing technology, this expansive molecular profiling delivers the critical clarity required to assess inherited susceptibilities, safely guiding customized cardiac oversight, proactive lifestyle adjustments, and specialized preventative treatments. Highly regarded for clinical excellence among the best diagnostic labs in the UAE, DNA Labs guarantees absolute patient confidentiality, exceptional analytical precision, and remarkably fast reporting. Take an empowered step toward cardiac wellness—schedule your cardiomyopathy genetics testing in UAE, coordinate a seamless home sample collection, or reach out to our dedicated genetics specialists today.

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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.