Diagnostic options · UAE

Genetic tests in Dubai & UAE

Compare available 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

805

Listed price range

600.00–30,000.00 AED

Clinical preparation

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Genetic test prices

Showing 586–600 of 805 matching tests.

Genetic diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4161 PRNP Gene Creutzfeldt-Jakob Disease Genetic Test This genetic test analyzes the PRNP gene for mutations linked to Creutzfeldt-Jakob disease, aiding in diagnosis and risk assessment.	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 ["PRNP gene pathogenic variants", "Inherited prion disorder risk"] Parameters [] Preparation ["Genetic Counselling & Pedigree Chart required prior to testing"] Indications ["Family history of CJD", "Unexplained progressive neurological symptoms", "Differential diagnosis of dementia"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: A81.0 Clinical summary This genetic test analyzes the PRNP gene for mutations linked to Creutzfeldt-Jakob disease, aiding in diagnosis and risk assessment.
TEST-4483 PRNP Gene Fatal Familial Insomnia Genetic Test This diagnostic test evaluates the PRNP gene for mutations associated with Fatal Familial Insomnia (FFI), a rare, inherited prion disease.	Whole Blood, Extracted DNA, or Dried Blood Spot on FTA Card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PRNP gene coding region", "Pathogenic variants (SNVs, indels, copy number changes)"] Parameters [] Preparation ["Pre-test genetic counselling recommended", "Detailed pedigree chart recommended"] Indications ["Family history of Fatal Familial Insomnia", "Clinical suspicion of FFI", "Differential diagnosis of dementia or sleep disorders"] Measurement technique Confirm with laboratory Codes LOINC: 23504-4 ICD-10: A81.83 Clinical summary This diagnostic test evaluates the PRNP gene for mutations associated with Fatal Familial Insomnia (FFI), a rare, inherited prion disease.
TEST-3758 PROKR2 Gene Hypogonadotropic Hypogonadism Type 3 (with or without Anosmia) Genetic Test This test evaluates the PROKR2 gene for pathogenic variants associated with hypogonadotropic hypogonadism type 3.	Whole Blood or 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 PROKR2 gene", "Single nucleotide variants", "Small deletions/duplications"] Parameters [] Preparation [] Indications ["Idiopathic hypogonadotropic hypogonadism", "Suspected Kallmann syndrome", "Family planning in affected families"] Measurement technique Confirm with laboratory Codes LOINC: 94716-0 ICD-10: E23.0 Clinical summary This test evaluates the PROKR2 gene for pathogenic variants associated with hypogonadotropic hypogonadism type 3.
TEST-2424 PROP1 Gene Pituitary Hormone Deficiency Type 2 Genetic Test This genetic test identifies mutations in the PROP1 gene associated with combined pituitary hormone deficiency type 2.	Peripheral whole blood (EDTA tube)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Mutations in the PROP1 gene", "Variant detection across coding exons"] Parameters [] Preparation ["No special fasting, dietary, or medication changes required"] Indications ["Clinical or biochemical suspicion of combined pituitary hormone deficiency type 2", "Congenital hypopituitarism"] Measurement technique Confirm with laboratory Codes LOINC: 103431-8 ICD-10: E23.0, Z15.89, Z13.79 Clinical summary This genetic test identifies mutations in the PROP1 gene associated with combined pituitary hormone deficiency type 2.
TEST-3568 PRPH2 Gene Choroidal Dystrophy, Central Areolar Type 2 (CACD2) Genetic Test This test evaluates the PRPH2 gene for mutations associated with Central Areolar Choroidal Dystrophy Type 2 (CACD2).	Peripheral Whole Blood	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PRPH2 gene mutations", "Copy Number Variations (CNV) in PRPH2"] Parameters [] Preparation [] Indications ["Clinical suspicion of Central Areolar Choroidal Dystrophy Type 2 (CACD2)", "Family history of inherited retinal disease"] Measurement technique Confirm with laboratory Codes LOINC: 84842-8 ICD-10: H31.21 Clinical summary This test evaluates the PRPH2 gene for mutations associated with Central Areolar Choroidal Dystrophy Type 2 (CACD2).
TEST-3657 PRPH2 Gene Sequencing (Fundus Albipunctatus) Genetic Test This test identifies pathogenic variants in the PRPH2 gene, confirming a diagnosis of fundus albipunctatus.	Peripheral Whole Blood, FTA Card Spot, or Extracted DNA	21 – 28 Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the PRPH2 gene"] Parameters [] Preparation ["Do not discontinue prescribed medication, eye drops, or therapy regimen without consulting your ophthalmologist."] Indications ["Suspected diagnosis of fundus albipunctatus", "Family history of fundus albipunctatus", "Need for genetic confirmation for monitoring and family planning"] Measurement technique Confirm with laboratory Codes LOINC: 52084-6 ICD-10: H35.52 Clinical summary This test identifies pathogenic variants in the PRPH2 gene, confirming a diagnosis of fundus albipunctatus.
TEST-3567 PRSS1 Gene Hereditary Pancreatitis Genetic Test This genetic test identifies pathogenic variants in the PRSS1 gene associated with hereditary pancreatitis.	Whole Blood, FTA Card or Extracted DNA	18–25 Working Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PRSS1 gene mutations", "Pathogenic variants"] Parameters [] Preparation ["Avoid alcohol 24 hours before sample collection", "Avoid high-fat meals 24 hours before sample collection", "Do not stop medications without physician consent"] Indications ["Diagnosis of hereditary pancreatitis", "Identification of individuals at risk for hereditary pancreatitis"] Measurement technique Confirm with laboratory Codes LOINC: 92263-1 ICD-10: K86.1 Clinical summary This genetic test identifies pathogenic variants in the PRSS1 gene associated with hereditary pancreatitis.
TEST-3601 PRSS2 Gene Susceptibility Test for Chronic Pancreatitis This test evaluates the PRSS2 gene for protective mutations associated with a reduced risk of chronic pancreatitis.	Whole Blood (Venous) or FTA Card (Dried Blood Spots)	16–20 Business Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PRSS2 gene mutations", "Protective genetic variants"] Parameters [] Preparation ["A detailed clinical history form is required", "A mandatory genetic counselling session is required"] Indications ["Individuals with a family history of chronic pancreatitis", "Patients with unexplained pancreatic disorders"] Measurement technique Confirm with laboratory Codes LOINC: 82298-6 ICD-10: K86.1 Clinical summary This test evaluates the PRSS2 gene for protective mutations associated with a reduced risk of chronic pancreatitis.
TEST-4136 PRX Gene Dejerine-Sottas Disease Genetic Test This test evaluates the PRX gene for pathogenic variants associated with Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III).	Whole Blood (Peripheral)	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 PRX gene", "Coding exons ±20 bp splice sites"] Parameters [] Preparation ["No fasting required", "Mandatory pre-test genetic counselling session"] Indications ["Suspected Dejerine-Sottas disease", "Family history of hereditary motor and sensory neuropathy type III"] Measurement technique Confirm with laboratory Codes LOINC: 48263-9 ICD-10: G60.0 Clinical summary This test evaluates the PRX gene for pathogenic variants associated with Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III).
TEST-5857 PSAP Gene (Prosaposin Deficiency) Genetic Test This genetic test evaluates the PSAP gene for mutations causing Prosaposin deficiency, a lysosomal storage disorder.	Whole blood, extracted DNA, or one drop blood on FTA card	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Disease-causing mutations in the PSAP gene", "Single-nucleotide variants", "Insertions and deletions (indels)"] Parameters [] Preparation [] Indications ["Suspected Prosaposin deficiency", "Confirmation of clinical diagnosis", "Family history of Prosaposin deficiency"] Measurement technique Confirm with laboratory Codes LOINC: 21667-9 ICD-10: E75.2 Clinical summary This genetic test evaluates the PSAP gene for mutations causing Prosaposin deficiency, a lysosomal storage disorder.
TEST-6142 PSAP Gene Sequencing for Atypical Krabbe Disease (NGS) Test This test identifies pathogenic mutations in the PSAP gene associated with atypical Krabbe disease (saposin C deficiency). It is used when standard enzyme assays for classic Krabbe...	Whole Blood (EDTA, 5–10 mL) or Oragene DNA Saliva Kit	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PSAP gene variants", "Saposin C function disruption"] Parameters [] Preparation ["Continue all prescribed medications", "Maintain seizure diary"] Indications ["Normal or equivocal GALC enzyme activity", "Suspected atypical Krabbe disease", "Carrier testing in families with known PSAP mutation", "Prenatal diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 94886-8 ICD-10: E75.23 Clinical summary This test identifies pathogenic mutations in the PSAP gene associated with atypical Krabbe disease (saposin C deficiency). It is used when standard enzyme assays for classic Krabbe disease are inconclusive.
TEST-5447 PSEN1 Gene Acne Inversa (Familial Type 3) Genetic Test This genetic test evaluates the PSEN1 gene for pathogenic variants associated with familial acne inversa (hidradenitis suppurativa) type 3.	Peripheral whole blood (EDTA tube) or FTA card finger-prick	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 PSEN1 gene", "Keratinocyte differentiation and immune function related to PSEN1"] Parameters [] Preparation ["No specific fasting required.", "Do not discontinue prescribed medications without consulting your physician."] Indications ["Clinical suspicion of familial acne inversa (hidradenitis suppurativa) type 3", "Family history of hidradenitis suppurativa", "Need for definitive diagnosis to guide treatment and family risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 91811-1 ICD-10: L73.2, Z82.2 Clinical summary This genetic test evaluates the PSEN1 gene for pathogenic variants associated with familial acne inversa (hidradenitis suppurativa) type 3.
TEST-4327 PSEN1 Gene Dilated Cardiomyopathy Type 1U (CMD1U) Genetic Test This test identifies pathogenic mutations in the PSEN1 gene associated with dilated cardiomyopathy type 1U.	Peripheral whole blood (3–5 mL EDTA tube)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PSEN1 gene mutations", "Pathogenic variants"] Parameters [] Preparation ["No fasting required", "No medication changes required", "Pre-genetic counselling session mandatory"] Indications ["Diagnosis of dilated cardiomyopathy type 1U", "Family screening for PSEN1-related cardiomyopathy", "Risk stratification in individuals with family history"] Measurement technique Confirm with laboratory Codes LOINC: 92830-2 ICD-10: I42.0 Clinical summary This test identifies pathogenic mutations in the PSEN1 gene associated with dilated cardiomyopathy type 1U.
TEST-2161 PTCH2 Gene (Gorlin Syndrome) Germline Mutation Genetic Test This genetic test evaluates the PTCH2 gene for germline mutations associated with Gorlin syndrome (Basal Cell Nevus Syndrome).	Peripheral whole blood (EDTA tube, 3–5 mL)	3 – 4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PTCH2 gene coding regions", "Exon-intron boundaries", "Single-nucleotide variants", "Small insertions/deletions", "Splice-site alterations"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Clinical suspicion of Gorlin syndrome", "Family history of Gorlin syndrome", "Multiple basal cell carcinomas", "Presence of characteristic features (e.g., jaw cysts, palmar/plantar pits)"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q85.01 Clinical summary This genetic test evaluates the PTCH2 gene for germline mutations associated with Gorlin syndrome (Basal Cell Nevus Syndrome).
TEST-3902 PTCHD1 Gene Genetic Test This test detects pathogenic variants, including single nucleotide variants and copy number variations, within the PTCHD1 gene.	Peripheral Whole Blood (EDTA) or Buccal Swab	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Single Nucleotide Variants (SNVs)", "Insertions/Deletions (Indels)", "Copy Number Variations (CNVs)"] Parameters [] Preparation ["No fasting required", "No cessation of routine medications required", "Mandatory pre-test genetic counseling session"] Indications ["Familial risk assessment for X-linked intellectual disability", "Personalized neurodevelopmental care planning", "Evaluation of autism spectrum disorder susceptibility"] Measurement technique Confirm with laboratory Codes LOINC: 96617-3 ICD-10: Z13.89 Clinical summary This test detects pathogenic variants, including single nucleotide variants and copy number variations, within the PTCHD1 gene.

Category overview

Genetic: overview

Unlocking the blueprint of your DNA provides profound, proactive insights into your family’s future and personal health risks. Integrated within our advanced Biochemistry and molecular services, specialized Genetic testing evaluates inherited traits, metabolic predispositions, and carrier statuses. Utilizing cutting-edge diagnostic technology, comprehensive genetic screening offers the vital clarity needed to safely guide tailored medical strategies and family planning. As an undisputed leader in innovation among diagnostic labs in Dubai and the UAE, DNA Labs guarantees the highest standards of strict patient confidentiality, unparalleled diagnostic precision, and rapid reporting. Empower your health decisions with certainty—book your genetic testing in UAE, coordinate a secure sample collection, or connect with our specialized genetics team today.

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