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DNA Labs India

Metabolic Disorders Wide Range Panel NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

Metabolic Disorders Wide Range Panel NGS Genetic Test

Short Name: Metabolic Disorders NGS Panel

Also known as: Metabolic Disorders Genetic Test, Wide Range Metabolic Panel NGS

Metabolic Disorders Wide Range Panel NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS Technology on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in 3 to 4 weeks. Free home collection in 300+ cities across India.

NGS Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of this test is to identify genetic mutations causing metabolic disorders through NGS, facilitating early diagnosis, genetic counseling, and informed healthcare decisions.

Test Code
1846
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
3 to 4 weeks
Fasting Required
No
Method
NGS Technology
Step 1

Sample Collection

Provide clinical history and undergo genetic counseling as required.

Method: Venipuncture or FTA card collection

Step 2

Laboratory Analysis

Blood sample collected via venipuncture or one drop on FTA card with minimal discomfort.

Step 3

Report Delivery

Sample processed in lab; reports delivered in 3-4 weeks.

Timeline: 3 to 4 weeks

Patient Instructions

1
Before the Test:Genetic counseling session to discuss family history and test implications.
2
During the Test:Sample collection procedure as per instructions.
3
After the Test:Follow-up with healthcare provider for result interpretation and management.

About This Test

Who Should Get This Test

The purpose of this test is to identify genetic mutations causing metabolic disorders through NGS, facilitating early diagnosis, genetic counseling, and informed healthcare decisions.

How to Prepare

  • Ensure proper sample labeling
  • Avoid hemolysis in blood samples
  • Store FTA cards at room temperature

Doctor's Notes

Reviewed by — MBBS, MD (Medical Genetics) · Reg. No. 8532

"This test is crucial for early diagnosis of metabolic disorders in families with a history or symptoms, aiding in genetic counseling and management planning."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
ContainerEDTA tube for blood samples
Collection MethodVenipuncture or FTA card collection

Sample Stability

Blood samples stable at 2-8°C for 48 hours
FTA cards stable at room temperature
Sample Rejection Criteria:
  • Hemolyzed samples
  • Incorrectly labeled samples
  • Insufficient sample volume

Understanding Your Results

Results indicate presence or absence of pathogenic variants in over 600 genes. Consult a geneticist for interpretation.
📊

No pathogenic variants detected

Low likelihood of genetic metabolic disorder based on tested genes

📊

Pathogenic variant detected

Diagnosis of specific metabolic disorder confirmed; genetic counseling recommended

📊

Variant of uncertain significance

Further testing or clinical correlation needed

⚠️ When to Consult a Doctor:

Consult a healthcare provider if symptoms persist or if genetic counseling is needed post-test.

Limitations

  • May not detect all rare mutations
  • Does not cover non-genetic causes of metabolic symptoms
  • Results require clinical correlation

Risks & Considerations

  • Minimal physical risk from blood draw
  • Potential psychological impact of results
  • Risk of uncertain findings

Interfering Factors

  • Sample contamination
  • Degraded DNA quality
  • Insufficient sample volume

Compare With Similar Tests

TestMetabolic Disorders Wide Range Panel NGS Genetic TestBasic Metabolic PanelTargeted Gene SequencingChromosomal MicroarrayBiochemical Enzyme Assays
ComparisonMetabolic Disorders Wide Range Panel NGS Genetic Test

Frequently Asked Questions

What is the Metabolic Disorders Wide Range Panel NGS Genetic Test?
It is a comprehensive genetic test using NGS to analyze over 600 genes for metabolic disorders.
Who should consider this test?
Individuals with symptoms like developmental delays, seizures, or a family history of metabolic disorders.
What sample is required?
Blood, extracted DNA, or one drop of blood on an FTA card.
Is fasting required for the test?
No, fasting is not mandatory.
How long does it take to get results?
Reports are delivered in 3 to 4 weeks.
What is the cost of the test?
The test costs INR 20000, including genetic counseling and home collection.
Is home sample collection available?
Yes, free home collection is offered across India for online bookings.
What disorders can this test diagnose?
It can diagnose disorders like PKU, galactosemia, maple syrup urine disease, and more.
How is the test performed?
Using next-generation sequencing (NGS) technology to identify gene mutations.
What if a variant of uncertain significance is found?
Consult a geneticist for further evaluation and possible additional testing.
Is genetic counseling included?
Yes, the cost includes a genetic counseling session.
Can this test be used for prenatal diagnosis?
It is primarily for postnatal diagnosis; consult a genetic counselor for prenatal options.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

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For Hospitals & Clinics

Reference Laboratory Services

We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.

LIMS Integration

Your Data Privacy

Your medical data is protected under Indian law.

Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.

DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.

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