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

Confirm test-specific instructions with your clinician or laboratory.

Compare available tests

Biochemistry test prices

Showing 976–990 of 1,113 matching tests.

Biochemistry diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-3170 Steroid Panel 2 (9 Steroids) Test This test quantitatively measures nine key serum steroids to evaluate adrenal and gonadal function and identify potential disorders.	Serum	3–4 working days	750.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Cortisol", "Dehydroepiandrosterone sulfate (DHEA-S)", "Androstenedione", "Total Testosterone", "Key biosynthetic precursors"] Parameters [{"name": "Cortisol", "reference_range": null}, {"name": "Dehydroepiandrosterone sulfate (DHEA-S)", "reference_range": null}, {"name": "Androstenedione", "reference_range": null}, {"name": "Total Testosterone", "reference_range": null}] Preparation ["Fasting for 10–12 hours is recommended", "Discontinue biotin-containing supplements for 72 hours prior", "Schedule venipuncture between 8–10 AM or 4–6 PM", "Avoid vigorous exercise and alcohol consumption for 24 hours before the test"] Indications ["Evaluation of adrenal axis disorders", "Evaluation of gonadal axis disorders", "Diagnosis of congenital adrenal hyperplasia", "Diagnosis of Cushing's syndrome", "Diagnosis of adrenal insufficiency", "Diagnosis of polycystic ovary syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 24319-0 ICD-10: E27.8 Clinical summary This test quantitatively measures nine key serum steroids to evaluate adrenal and gonadal function and identify potential disorders.
TEST-3166 Steroid Panel 3 (15 Steroids) Test This test evaluates adrenal and gonadal steroid hormone levels using LC-MS/MS technology.	Serum	2–3 business days	850.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Adrenal Steroids", "Gonadal Steroids", "Steroidogenesis Pathway"] Parameters [] Preparation ["Collect sample between 8–10 AM or 4–6 PM", "Do not discontinue prescribed medication without consulting your doctor"] Indications ["Diagnosis of adrenal dysfunction", "Assessment of performance-related imbalances", "Detection of exogenous steroid use", "Diagnosis of conditions like Cushing’s syndrome, adrenal insufficiency, PCOS"] Measurement technique Confirm with laboratory Codes LOINC: 94306-8 ICD-10: E27.9, R79.89 Clinical summary This test evaluates adrenal and gonadal steroid hormone levels using LC-MS/MS technology.
TEST-3175 Steroid Panel for Congenital Adrenal Hyperplasia (CAH) Test This diagnostic test evaluates adrenal function by quantifying key steroid hormones to identify Congenital Adrenal Hyperplasia (CAH). It provides highly specific and sensitive resu...	Serum	2–3 business days (sample Mon/Thu by 9 AM → report Wed/Sat)	900.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["17‑hydroxyprogesterone", "Androstenedione", "Cortisol", "Adrenal steroid levels"] Parameters [{"name": "17-hydroxyprogesterone", "reference_range": null}, {"name": "Androstenedione", "reference_range": null}, {"name": "Cortisol", "reference_range": null}] Preparation ["Collect sample during recommended diurnal window (8-10 AM or 4-6 PM)", "Avoid collecting sample in SST gel barrier tubes", "Inform lab of any interfering medications"] Indications ["Newborn screening follow-up", "Confirmatory testing for suspected CAH", "Therapeutic monitoring of CAH treatment", "Evaluation of adrenal disorders"] Measurement technique Confirm with laboratory Codes LOINC: 96368-7 ICD-10: E25.9 Clinical summary This diagnostic test evaluates adrenal function by quantifying key steroid hormones to identify Congenital Adrenal Hyperplasia (CAH). It provides highly specific and sensitive results compared to traditional immunoassays.
TEST-3171 Steroid Panel for PCOS & Non-Classical CAH Differentiation Test This diagnostic test evaluates adrenal and ovarian steroid hormone levels to differentiate between PCOS and Non-Classical CAH.	Serum (Red Top, No Additive tube — 2 mL, 1 mL minimum)	3–5 business days (specimen collected Mon/Thu by 9 AM)	800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["17-hydroxyprogesterone", "Androstenedione", "Cortisol", "Adrenal and ovarian hormones"] Parameters [{"name": "17-hydroxyprogesterone", "reference_range": null}, {"name": "Androstenedione", "reference_range": null}, {"name": "Cortisol", "reference_range": null}, {"name": "Other key adrenal and ovarian hormones", "reference_range": null}] Preparation ["No fasting required", "Sample collection between 8–10 AM", "Menstruating females should provide sample within the first 10 days of their menstrual cycle"] Indications ["Differentiation between PCOS and NCCAH", "Evaluation of suspected adrenal or ovarian steroid abnormalities"] Measurement technique Confirm with laboratory Codes LOINC: 96295-3 ICD-10: E28.2, E25.0 Clinical summary This diagnostic test evaluates adrenal and ovarian steroid hormone levels to differentiate between PCOS and Non-Classical CAH.
TEST-3179 Steroid Panel for Premature Adrenarche Test This diagnostic test evaluates adrenal androgen levels to identify the cause of premature adrenarche.	Peripheral whole blood (Serum/Plasma)	3–4 working days (Mon/Thu by 9 am)	800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["DHEA-S", "Androstenedione", "Testosterone", "Adrenal Androgens"] Parameters [{"name": "DHEA-S", "reference_range": null}, {"name": "Androstenedione", "reference_range": null}, {"name": "Testosterone", "reference_range": null}] Preparation ["Sample drawn between 8–10 am or 4–6 pm", "No special dietary preparation required", "Keep child well-hydrated"] Indications ["Evaluation of premature adrenarche", "Distinguishing benign premature adrenarche from late-onset congenital adrenal hyperplasia", "Screening for androgen-secreting tumors"] Measurement technique Confirm with laboratory Codes LOINC: 101388-7 ICD-10: E27.0 Clinical summary This diagnostic test evaluates adrenal androgen levels to identify the cause of premature adrenarche.
TEST-3176 Steroid Panel: 21‑Hydroxylase Deficiency Test This diagnostic test evaluates adrenal steroid levels to diagnose 21-hydroxylase deficiency, a form of congenital adrenal hyperplasia (CAH). It measures key hormones like 17-hydrox...	Blood (Serum)	3–4 working days	650.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["17‑hydroxyprogesterone", "Androstenedione", "Cortisol"] Parameters [{"name": "17‑hydroxyprogesterone", "reference_range": "0.05–0.1 ng/mL"}, {"name": "Androstenedione", "reference_range": null}, {"name": "Cortisol", "reference_range": null}] Preparation ["Fast for 8 hours.", "Draw blood between 8‑10 AM.", "Disclose corticosteroid use to your doctor.", "Avoid SST gel‑barrier tubes; use a plain red‑top serum tube.", "Refrigerate or freeze sample immediately after collection."] Indications ["Diagnosis of Congenital Adrenal Hyperplasia (CAH)", "Evaluation of ambiguous genitalia", "Monitoring glucocorticoid replacement therapy"] Measurement technique Confirm with laboratory Codes LOINC: 20574-3 ICD-10: E25.0 Clinical summary This diagnostic test evaluates adrenal steroid levels to diagnose 21-hydroxylase deficiency, a form of congenital adrenal hyperplasia (CAH). It measures key hormones like 17-hydroxyprogesterone, androstenedione, and cortisol.
TEST-4273 STXBP1 Gene (Early Infantile Epileptic Encephalopathy Type 4) Genetic Test This test identifies pathogenic mutations in the STXBP1 gene associated with early infantile epileptic encephalopathy type 4 (EIEE4). It uses Next-Generation Sequencing (NGS) with...	Whole Blood (EDTA), Extracted Genomic DNA, or FTA Card Dried Blood Spot	3–4 weeks (21–28 business days)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["STXBP1 gene coding region", "STXBP1 gene splice-site boundaries"] Parameters [] Preparation ["No fasting or special dietary preparation is needed.", "Mandatory pre-test genetic counselling session must be completed before sample collection."] Indications ["Diagnosis of early infantile epileptic encephalopathy type 4 (EIEE4)", "Identification of pathogenic STXBP1 mutations"] Measurement technique Confirm with laboratory Codes LOINC: 94058-8 ICD-10: G40.4 Clinical summary This test identifies pathogenic mutations in the STXBP1 gene associated with early infantile epileptic encephalopathy type 4 (EIEE4). It uses Next-Generation Sequencing (NGS) with Sanger confirmation for clinically actionable variants.
TEST-3195 Succinylacetone Blood Test This test measures the level of succinylacetone in a dried blood spot sample to screen for and diagnose Tyrosinemia Type I.	Dried Blood Spot (Heel/Finger Prick) on Filter Paper	4 days (Monday/Thursday collection cut-off)	850.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Succinylacetone levels", "Metabolic pathway dysfunction related to Tyrosinemia Type I"] Parameters [{"name": "Succinylacetone", "reference_range": null}] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Screening for Tyrosinemia Type I", "Diagnosis of Tyrosinemia Type I", "Monitoring treatment response in Tyrosinemia Type I"] Measurement technique Confirm with laboratory Codes LOINC: 104570-3 ICD-10: E70.21 Clinical summary This test measures the level of succinylacetone in a dried blood spot sample to screen for and diagnose Tyrosinemia Type I.
TEST-3192 Succinylacetone Urine Test This diagnostic test evaluates the concentration of succinylacetone in urine, a key biomarker for Hereditary Tyrosinemia Type I.	Random urine (10 mL)	3–4 working days (Mon/Thu by 9 am; Report Thu/Mon)	850.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Succinylacetone levels", "Fumarylacetoacetate hydrolase (FAH) enzyme deficiency indicator"] Parameters [{"name": "Succinylacetone", "reference_range": null}] Preparation ["Collect 10 mL of random urine in a sterile screw-capped container.", "No preservatives in the container.", "Refrigerate sample immediately at 2–8°C.", "No dietary restrictions required.", "Provide clinical history including symptoms and family history."] Indications ["Suspected Hereditary Tyrosinemia Type I (HT-1)", "Screening for metabolic disorders", "Evaluation of liver dysfunction in infants", "Assessment of neurological symptoms in infants"] Measurement technique Confirm with laboratory Codes LOINC: 32624-8 ICD-10: E70.21 Clinical summary This diagnostic test evaluates the concentration of succinylacetone in urine, a key biomarker for Hereditary Tyrosinemia Type I.
TEST-6392 SUGCT Gene Glutaric Aciduria Type 3 Genetic Test This genetic test identifies pathogenic variants in the SUGCT gene, confirming a diagnosis of glutaric aciduria type 3.	Peripheral Whole Blood (3–5 mL in EDTA tube); alternative: buccal swab for neonates	3–4 Weeks (expedited reporting for critically ill neonates)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SUGCT gene sequence", "Pathogenic variants (point mutations, indels, CNVs)"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication without consulting a specialist"] Indications ["Suspected glutaric aciduria type 3", "Family history of glutaric aciduria type 3", "Inconclusive biochemical screening"] Measurement technique Confirm with laboratory Codes LOINC: 94222-3 ICD-10: E72.52 Clinical summary This genetic test identifies pathogenic variants in the SUGCT gene, confirming a diagnosis of glutaric aciduria type 3.
TEST-3575 SULT2A1 Gene Polycystic Ovary Syndrome Type 1 Genetic Test This test identifies pathogenic variants in the SULT2A1 gene associated with type 1 Polycystic Ovary Syndrome (PCOS). It uses Next-Generation Sequencing (NGS) to detect mutations l...	Peripheral whole blood (also accepted: extracted DNA, FTA card)	3 – 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SULT2A1 gene variants", "Pathogenic mutations associated with PCOS"] Parameters [] Preparation ["No specific fasting required", "No medication or diet changes needed"] Indications ["Diagnosis of type 1 PCOS", "Familial risk assessment for PCOS", "Fertility planning", "Guiding precision therapy"] Measurement technique Confirm with laboratory Codes LOINC: 86727-5 ICD-10: E28.2 Clinical summary This test identifies pathogenic variants in the SULT2A1 gene associated with type 1 Polycystic Ovary Syndrome (PCOS). It uses Next-Generation Sequencing (NGS) to detect mutations linked to hyperandrogenism.
TEST-5904 SYNE1 Gene Spinocerebellar Ataxia Type 8 (Autosomal Recessive) Genetic Test This genetic test identifies pathogenic variants in the SYNE1 gene associated with autosomal recessive spinocerebellar ataxia type 8 (SCAR8).	Peripheral Whole Blood or 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 SYNE1 gene", "Coding region and splice sites coverage"] Parameters [] Preparation ["No fasting required", "Bring valid Emirates ID, insurance card, and completed genetic counselling referral form", "Avoid heavy muscular exertion immediately before collection"] Indications ["Suspected diagnosis of Spinocerebellar Ataxia Type 8 (SCAR8)", "Family history of SCAR8", "Progressive neurological symptoms consistent with SCAR8"] Measurement technique Confirm with laboratory Codes LOINC: 83511-4 ICD-10: G11.8, R27.0 Clinical summary This genetic test identifies pathogenic variants in the SYNE1 gene associated with autosomal recessive spinocerebellar ataxia type 8 (SCAR8).
TEST-4224 TAB2 Gene (Congenital Heart Defects, Multiple Types) Genetic Test This genetic test evaluates the TAB2 gene for pathogenic variants associated with multiple types of congenital heart defects.	Peripheral Blood (Whole 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 TAB2 gene", "Single nucleotide variants (SNVs)", "Insertions", "Deletions", "Copy number variants"] Parameters [] Preparation ["No fasting required", "Pre-test genetic counselling is mandatory"] Indications ["Diagnosis of congenital heart defects", "Risk assessment for family members", "Informed family planning", "Correlation with echocardiographic findings"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q24.9 Clinical summary This genetic test evaluates the TAB2 gene for pathogenic variants associated with multiple types of congenital heart defects.
TEST-4748 TACO1 Gene Analysis for Leigh Syndrome (Mitochondrial Complex IV Deficiency) Test This test identifies pathogenic variants in the TACO1 gene, a known cause of Leigh syndrome associated with mitochondrial complex IV deficiency.	Whole blood (EDTA tube), extracted DNA, dried blood spot (FTA card)	21–28 business days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TACO1 gene sequence", "Point mutations", "Small insertions/deletions", "Canonical splice-site variants"] Parameters [] Preparation ["Inform clinician of all current medications, dietary supplements.", "Inform clinician of any organ transplantation or blood transfusion within the preceding two weeks."] Indications ["Suspected Leigh Syndrome", "Mitochondrial Complex IV Deficiency", "Family history of Leigh Syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 94872-0 ICD-10: E88.41 Clinical summary This test identifies pathogenic variants in the TACO1 gene, a known cause of Leigh syndrome associated with mitochondrial complex IV deficiency.
TEST-3720 TACR3 Gene Hypogonadotropic Hypogonadism Type 11 Genetic Test This diagnostic test evaluates the TACR3 gene for mutations associated with congenital hypogonadotropic hypogonadism type 11.	Peripheral Whole 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 TACR3 gene", "Coding exons, intronic boundaries, and known regulatory regions"] Parameters [] Preparation ["No special preparation or fasting required", "Inform phlebotomist of current medications"] Indications ["Delayed puberty", "Anosmia", "Unexplained infertility", "Family history of hypogonadotropic hypogonadism"] Measurement technique Confirm with laboratory Codes LOINC: 81265-7 ICD-10: E23.0 Clinical summary This diagnostic test evaluates the TACR3 gene for mutations associated with congenital hypogonadotropic hypogonadism type 11.

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.

Before booking

Use the test details as a conversation starter

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.

Explore this area

Biochemistry tests in Dubai & UAE

Biochemistry test prices

Biochemistry: overview

Use the test details as a conversation starter

Related Biochemistry categories