Biochemistry tests in Dubai & UAE

Compare available Biochemistry 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

1,113

Listed price range

450.00–30,000.00 AED

Clinical preparation

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Biochemistry test prices

Showing 1051–1065 of 1,113 matching tests.

Biochemistry diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-2413 TUBA8 Gene Polymicrogyria with Optic Nerve Hypoplasia Genetic Test This genetic test analyzes the TUBA8 gene to detect mutations associated with polymicrogyria and optic nerve hypoplasia.	Peripheral Whole Blood	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TUBA8 gene sequence", "Copy Number Variations (CNVs) in TUBA8"] Parameters [] Preparation ["No specific patient preparation required"] Indications ["Suspected genetic cause of polymicrogyria with optic nerve hypoplasia", "Differential diagnosis of brain malformations"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q04.3, H47.0 Clinical summary This genetic test analyzes the TUBA8 gene to detect mutations associated with polymicrogyria and optic nerve hypoplasia.
TEST-4265 TUBB4A Gene DYT4 Next‑Generation Sequencing Genetic Test This genetic test evaluates the TUBB4A gene for mutations associated with DYT4 dystonia.	Whole Blood or Buccal Swab	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TUBB4A gene sequence", "Pathogenic variants (SNVs, indels, CNVs)"] Parameters [] Preparation ["No fasting required"] Indications ["Suspected DYT4 dystonia", "Positive family history of dystonia", "Need for definitive molecular diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 90553-4 ICD-10: G24.1 Clinical summary This genetic test evaluates the TUBB4A gene for mutations associated with DYT4 dystonia.
TEST-2776 Tuberous Sclerosis Complex (TSC) Genetic Testing Test This test detects pathogenic variants in the TSC1 and TSC2 genes associated with Tuberous Sclerosis Complex.	Peripheral whole blood	30 working days	3,100.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in TSC1 gene", "Pathogenic variants in TSC2 gene", "Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Copy number variations (CNVs)"] Parameters [] Preparation ["No fasting required", "Complete the Clinical Exome Testing Requisition Form (Form 36)"] Indications ["Clinical suspicion of TSC based on diagnostic criteria", "Prenatal counseling for families with TSC history", "Determining eligibility for mTOR inhibitor therapy", "Recurrence risk assessment for family members"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q85.1 Clinical summary This test detects pathogenic variants in the TSC1 and TSC2 genes associated with Tuberous Sclerosis Complex.
TEST-2580 TUBGCP6 Gene Microcephaly, Chorioretinopathy & Intellectual Disability Genetic Test This genetic test evaluates the TUBGCP6 gene for variants associated with microcephaly, chorioretinopathy, and intellectual disability.	Whole Blood (EDTA), Extracted DNA, Dried Blood Spot (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 TUBGCP6 gene", "Deletions/Duplications in the TUBGCP6 gene"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Suspected TUBGCP6-related disorder", "Family history of TUBGCP6-related disorder", "Genetic counselling for affected families"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Q02, H31.1, F79 Clinical summary This genetic test evaluates the TUBGCP6 gene for variants associated with microcephaly, chorioretinopathy, and intellectual disability.
TEST-6264 TUFM Gene Combined Oxidative Phosphorylation Deficiency Type 4 Genetic Test This test identifies genetic variants in the TUFM gene associated with Combined Oxidative Phosphorylation Deficiency Type 4 (COXPD4).	Whole Blood (3-5 mL) or Buccal Swab (FTA Card)	3 – 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TUFM gene sequence", "Copy Number Variations (CNV) in TUFM gene"] Parameters [] Preparation ["No fasting required", "No medication adjustments required unless specifically instructed by your doctor"] Indications ["Unexplained mitochondrial encephalopathy", "Lactic acidosis", "Neurodevelopmental regression", "Family history of mitochondrial disorders"] Measurement technique Confirm with laboratory Codes LOINC: 105406-5 ICD-10: E88.49 Clinical summary This test identifies genetic variants in the TUFM gene associated with Combined Oxidative Phosphorylation Deficiency Type 4 (COXPD4).
TEST-4992 TUSC3 Gene Mental Retardation, Autosomal Recessive Type 7 Genetic Test This genetic test identifies pathogenic variants in the TUSC3 gene, which are associated with autosomal recessive mental retardation type 7.	Peripheral Whole Blood (EDTA)	21–28 Days (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 TUSC3 gene"] Parameters [] Preparation [] Indications ["Differential diagnosis of neurodevelopmental delay", "Family risk assessment for autosomal recessive mental retardation type 7"] Measurement technique Confirm with laboratory Codes LOINC: 94500-0 ICD-10: F78.9, Z14.8, Z82.79 Clinical summary This genetic test identifies pathogenic variants in the TUSC3 gene, which are associated with autosomal recessive mental retardation type 7.
TEST-4911 TYK2 Gene (Autosomal Recessive Immunodeficiency Type 35) Genetic Test This genetic test analyzes the TYK2 gene to identify mutations causing autosomal recessive immunodeficiency type 35.	Peripheral Whole Blood (3–5 mL in EDTA tube); also accepted: extracted DNA (2 µg) 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 ["TYK2 gene coding regions", "TYK2 gene flanking intronic regions"] Parameters [] Preparation ["Informed consent and pre-test genetic counselling are mandatory prior to sample collection"] Indications ["Clinical suspicion of TYK2-related immunodeficiency", "Family history of TYK2-related immunodeficiency", "Recurrent severe infections", "Early-onset atopic dermatitis"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: D81.8 Clinical summary This genetic test analyzes the TYK2 gene to identify mutations causing autosomal recessive immunodeficiency type 35.
TEST-5473 TYR Gene Albinism (Oculocutaneous Type 1A) Genetic Test This test evaluates the entire TYR gene for mutations associated with oculocutaneous albinism type 1A (OCA1A). It provides a definitive molecular diagnosis.	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 TYR gene"] Parameters [] Preparation ["No fasting required"] Indications ["Suspected diagnosis of oculocutaneous albinism type 1A", "Family history of OCA1A", "Genetic counselling for individuals with albinism features"] Measurement technique Confirm with laboratory Codes LOINC: 93390-5 ICD-10: E70.320, H53.8, Z15.09 Clinical summary This test evaluates the entire TYR gene for mutations associated with oculocutaneous albinism type 1A (OCA1A). It provides a definitive molecular diagnosis.
TEST-5484 TYROBP Gene PLOSL (Nasu‑Hakola Disease) Genetic Test This genetic test evaluates the entire coding region of the TYROBP gene to detect pathogenic variants associated with Nasu‑Hakola disease.	Whole Blood (3–4 mL in DNA tube), 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 ["TYROBP gene coding region", "Pathogenic variants (SNVs, indels, CNVs)"] Parameters [] Preparation [] Indications ["Suspected Nasu‑Hakola disease", "Family history of Nasu‑Hakola disease", "Evaluation of unexplained bone lesions or young-onset dementia"] Measurement technique Confirm with laboratory Codes LOINC: 81321-6 ICD-10: E75.2 Clinical summary This genetic test evaluates the entire coding region of the TYROBP gene to detect pathogenic variants associated with Nasu‑Hakola disease.
TEST-4892 UBE2A Gene Nascimento-Type X-Linked Syndromic Mental Retardation Genetic Test This test evaluates the UBE2A gene for pathogenic variants associated with Nascimento-type X-linked syndromic mental retardation.	Peripheral blood (EDTA tube) 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 ["UBE2A gene variants", "Single nucleotide variants", "Small insertions/deletions", "Large copy number changes"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any relevant medications"] Indications ["Suspected Nascimento-type X-linked syndromic mental retardation", "Family history of the condition", "Genetic counselling for at-risk families"] Measurement technique Confirm with laboratory Codes LOINC: 81314-0 ICD-10: Q87.8 Clinical summary This test evaluates the UBE2A gene for pathogenic variants associated with Nascimento-type X-linked syndromic mental retardation.
TEST-3863 UGT1A1 Gene Crigler-Najjar Syndrome Type 1 Genetic Test This genetic test identifies pathogenic variants in the UGT1A1 gene associated with Crigler-Najjar syndrome type 1.	Venous Blood or FTA Card (Dried Blood Spot)	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 UGT1A1 gene", "Presence of mutations causing Crigler-Najjar syndrome type 1"] Parameters [] Preparation ["Pre-genetic counseling session required", "Document family history of UGT1A1-related jaundice"] Indications ["Suspected Crigler-Najjar syndrome type 1", "Severe neonatal jaundice unresponsive to standard treatment", "Family history of UGT1A1-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 48807-8 ICD-10: E80.5 Clinical summary This genetic test identifies pathogenic variants in the UGT1A1 gene associated with Crigler-Najjar syndrome type 1.
TEST-3805 UGT1A1 Gene Gilbert Syndrome Genetic Test This genetic test identifies variants in the UGT1A1 gene associated with Gilbert syndrome.	Peripheral whole blood (EDTA) or FTA blood spot card	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["UGT1A1 gene variants", "Promoter TATA box variants", "Exonic variants", "Intronic boundary variants", "Copy number variations (CNV)"] Parameters [] Preparation [] Indications ["Diagnosis of Gilbert syndrome", "Evaluation of mild unconjugated hyperbilirubinemia"] Measurement technique Confirm with laboratory Codes LOINC: 77745-3 ICD-10: E80.4, Z14.8, Z13.79 Clinical summary This genetic test identifies variants in the UGT1A1 gene associated with Gilbert syndrome.
TEST-3794 UGT1A1 Gene Hyperbilirubinemia (Familial Transient Neonatal) Genetic Test This diagnostic test evaluates the UGT1A1 gene for variants associated with familial transient neonatal hyperbilirubinemia.	Peripheral Whole Blood, Dried Blood Spot (FTA Card)	10-14 Business Days (ISO Fast Track)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["UGT1A1 gene sequence", "Single Nucleotide Variants (SNVs)", "Insertions and Deletions (Indels)", "Copy Number Variations (CNVs)"] Parameters [] Preparation ["No specific fasting required for newborns.", "Inform the lab about any recent blood transfusions."] Indications ["Infants with severe or prolonged neonatal jaundice", "Family history of familial transient neonatal hyperbilirubinemia", "Need for definitive molecular diagnosis to guide management"] Measurement technique Confirm with laboratory Codes LOINC: 21748-8 ICD-10: E80.4 Clinical summary This diagnostic test evaluates the UGT1A1 gene for variants associated with familial transient neonatal hyperbilirubinemia.
TEST-3640 UMOD Gene Medullary Cystic Kidney Disease Type 2 Genetic Test This test identifies mutations in the UMOD gene associated with Medullary Cystic Kidney Disease Type 2.	Whole blood, 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 ["UMOD gene mutations", "Autosomal dominant tubulointerstitial kidney disease"] Parameters [] Preparation ["No fasting or special preparation needed"] Indications ["Family history of unexplained chronic kidney disease", "Family history of early-onset gout", "Family history of medullary cysts", "Suspicion of Medullary Cystic Kidney Disease Type 2"] Measurement technique Confirm with laboratory Codes LOINC: 92907-8 ICD-10: Q61.5 Clinical summary This test identifies mutations in the UMOD gene associated with Medullary Cystic Kidney Disease Type 2.
TEST-3913 UNC13B Gene Genetic Test for Autism This test evaluates the UNC13B gene for pathogenic variants associated with Autism Spectrum Disorder (ASD). It uses Next-Generation Sequencing (NGS) to identify mutations.	EDTA Whole Blood, Dried Blood Spot, or Extracted DNA	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["UNC13B gene coding region", "Pathogenic variants (SNVs, indels)"] Parameters [] Preparation ["No fasting required", "Provide previous neurodevelopmental assessments", "Provide family history"] Indications ["Suspected genetic cause of Autism Spectrum Disorder", "Family history of ASD", "Risk assessment for family members"] Measurement technique Confirm with laboratory Codes LOINC: 21770-0 ICD-10: F84.0 Clinical summary This test evaluates the UNC13B gene for pathogenic variants associated with Autism Spectrum Disorder (ASD). It uses Next-Generation Sequencing (NGS) to identify mutations.

Category overview

Biochemistry: overview

Seeking clarity about your body's essential functions is vital for long-term well-being. At DNA Labs UAE, our Biochemistry services utilize advanced automated analyzers to evaluate enzymes, proteins, and metabolites in your blood. Whether you need routine metabolic panels or specialized biochemical testing in the UAE, these tests provide critical data to guide your physician's medical plan. As a leading diagnostic lab in Dubai and the UAE, we guarantee strict confidentiality and rapid, accurate turnaround times. Take charge of your health today. Explore our biochemistry diagnostics below, schedule a convenient home sample collection, or contact our specialists to book your test.

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Biochemistry tests in Dubai & UAE

Biochemistry test prices

Biochemistry: overview

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