Metabolic Genetic tests in Dubai & UAE

Compare available Metabolic Genetic tests, their listed prices and the information provided for each option. Test selection and preparation should be discussed with your clinician.

Tests in this category

Listed price range

2,800.00 AED

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Metabolic Genetic test prices

Showing 1–6 of 6 matching tests.

Metabolic Genetic diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-6082 AMACR Gene Sequencing (Alpha-Methylacyl-CoA Racemase Deficiency) Test This test analyzes the AMACR gene for pathogenic variants associated with Alpha-Methylacyl-CoA Racemase Deficiency.	Blood (2–5 ml EDTA), Extracted DNA (1–2 µg), 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 AMACR gene", "Deletion/duplication analysis of the AMACR gene"] Parameters [] Preparation [] Indications ["Diagnosis of Alpha-Methylacyl-CoA Racemase Deficiency", "Evaluation of adult-onset neuropathy", "Investigation of bile acid synthesis defects"] Measurement technique Confirm with laboratory Codes LOINC: 94293-0 ICD-10: E71.6 Clinical summary This test analyzes the AMACR gene for pathogenic variants associated with Alpha-Methylacyl-CoA Racemase Deficiency.
TEST-6267 BAAT Gene Hypercholanemia Genetic Test This test evaluates the BAAT gene for mutations associated with hypercholanemia, a rare bile acid metabolism disorder.	Whole Blood (Peripheral Blood)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["BAAT gene pathogenic variants", "Bile acid metabolism pathway integrity"] Parameters [] Preparation ["Pre-test genetic counselling is mandatory", "Informed consent required"] Indications ["Suspected hypercholanemia", "Family history of bile acid disorders", "Unexplained cholestasis", "Liver disease of unknown origin"] Measurement technique Confirm with laboratory Codes LOINC: 82342-1 ICD-10: E80.7 Clinical summary This test evaluates the BAAT gene for mutations associated with hypercholanemia, a rare bile acid metabolism disorder.
TEST-6118 COQ6 Gene Primary Coenzyme Q10 Deficiency Type 6 Genetic Test This genetic test identifies pathogenic variants in the COQ6 gene, confirming a diagnosis of primary coenzyme Q10 deficiency type 6.	Peripheral Whole Blood (3–5 mL EDTA) or DNA FTA card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["COQ6 gene sequence", "Pathogenic variants in COQ6"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of recent blood transfusions"] Indications ["Suspected primary coenzyme Q10 deficiency type 6", "Family history of the disorder", "Need for genetic confirmation"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: E63.8 Clinical summary This genetic test identifies pathogenic variants in the COQ6 gene, confirming a diagnosis of primary coenzyme Q10 deficiency type 6.
TEST-6348 ETFDH Gene Glutaric Acidemia Type 2C Genetic Test This diagnostic assay evaluates the ETFDH gene for pathogenic variants associated with Glutaric Acidemia Type 2C (GA2C), a rare metabolic disorder.	Peripheral Whole Blood (EDTA, 3–5 mL)	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 ETFDH gene", "Copy Number Variations (CNVs) within the ETFDH gene"] Parameters [] Preparation ["No fasting required", "No medication adjustments unless advised by metabolic specialist", "Provide prior biochemical test results (plasma acylcarnitine profile, urinary organic acids) if available", "Provide a three-generation pedigree if available"] Indications ["Suspected Glutaric Acidemia Type 2C based on clinical presentation", "Abnormal newborn screening results", "Family history of Glutaric Acidemia Type 2C", "Carrier screening for at-risk individuals"] Measurement technique Confirm with laboratory Codes LOINC: 82319-6 ICD-10: E71.3 Clinical summary This diagnostic assay evaluates the ETFDH gene for pathogenic variants associated with Glutaric Acidemia Type 2C (GA2C), a rare metabolic disorder.
TEST-6041 MMADHC Gene Methylmalonic Aciduria CblD Type Next-Generation Sequencing (NGS) Genetic Test This test identifies pathogenic variants in the MMADHC gene, which are responsible for causing methylmalonic aciduria and homocystinuria, CblD type.	Peripheral Whole Blood (venous collection) or FTA card	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 MMADHC gene", "Single Nucleotide Variants (SNVs)", "Insertions/Deletions (indels)", "Copy Number Changes"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Suspected diagnosis of methylmalonic aciduria and homocystinuria, CblD type", "Family history of the disorder", "Confirmation of diagnosis based on biochemical testing"] Measurement technique Confirm with laboratory Codes LOINC: 85913-5 ICD-10: E71.128, Z15.09, E71.120 Clinical summary This test identifies pathogenic variants in the MMADHC gene, which are responsible for causing methylmalonic aciduria and homocystinuria, CblD type.
TEST-5939 MTTP Gene Sequencing for Abetalipoproteinemia Test This test identifies pathogenic variants in the MTTP gene associated with abetalipoproteinemia.	Whole Blood, DNA FTA Card, or Extracted DNA (Peripheral 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 MTTP gene", "Copy Number Variations (CNV) in the MTTP gene"] Parameters [] Preparation ["No specific fasting required", "Continue all prescribed medications"] Indications ["Suspected abetalipoproteinemia", "Family history of abetalipoproteinemia", "Need for definitive molecular diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: E78.6 Clinical summary This test identifies pathogenic variants in the MTTP gene associated with abetalipoproteinemia.

Category overview

Metabolic Genetic: overview

Pinpointing the exact hereditary enzyme deficiency driving a metabolic crisis is the key to preventing irreversible damage and unlocking precise, life-saving therapies. As a highly focused diagnostic tool in our Molecular Genetics department, Metabolic Genetic testing specifically targets the exact DNA mutations responsible for your family's unique biochemical presentation. By leveraging advanced sequencing technology, this precise genomic screening confirms the exact metabolic block, offering the critical clarity required to assess carrier status, safely guide customized nutritional interventions, and evaluate risks for future children. Highly regarded for specialized diagnostic excellence among top diagnostic labs in the UAE, DNA Labs guarantees absolute patient confidentiality, exceptional analytical precision, and remarkably fast turnaround times. Take control of your long-term metabolic health—schedule your metabolic genetic testing in UAE, coordinate a comfortable home sample collection, or connect with our specialized genetic counselors.

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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.