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DNA Labs India

Complete Inherited Disease Panel Test

DNA Labs India | ISO 9001:2015 Certified

Complete Inherited Disease Panel Test

Short Name: Inherited Disease Panel

Complete Inherited Disease Panel Test test available at DNA Labs India for ₹36,000. Uses Next-Generation Sequencing (NGS) on Amniotic fluid, Chorionic villi, Peripheral blood samples. Results in 4-6 weeks. Free home collection in 300+ cities across India.

Genetic TestAll Ages🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of the Complete Inherited Disease Panel is to diagnose inherited diseases by identifying genetic mutations in an individual's DNA. It helps detect conditions that may be passed down in families, allowing for early intervention, personalized treatment, and management of symptoms to improve quality of life.

Test Code
2985
Price
₹36,000
Sample Type
Amniotic fluid, Chorionic villi, Peripheral blood
Result Time
4-6 weeks
Fasting Required
No
Method
Next-Generation Sequencing (NGS)
Step 1

Sample Collection

Doctor's prescription is required. Prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.

Method: Blood draw, Amniocentesis, Chorionic Villus Sampling

Step 2

Laboratory Analysis

Your sample is analyzed using Next-Generation Sequencing (NGS) in our laboratory.

Step 3

Report Delivery

A certified pathologist reviews and signs your report. You receive it as a secure PDF via email and WhatsApp.

Timeline: 4-6 weeks

Patient Instructions

1
Before the Test:Doctor's prescription is required. Prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.

About This Test

Who Should Get This Test

The purpose of the Complete Inherited Disease Panel is to diagnose inherited diseases by identifying genetic mutations in an individual's DNA. It helps detect conditions that may be passed down in families, allowing for early intervention, personalized treatment, and management of symptoms to improve quality of life.

How to Prepare

  • Sample must be collected in sterile containers.
  • For blood samples, use EDTA vacutainer.
  • Maintain sample integrity during transport with cool packs if needed.

Doctor's Notes

Reviewed by — MBBS, MD (Pathology) · Reg. No. 21521

"This panel is crucial for families with a history of genetic disorders, enabling early diagnosis and management for better health outcomes."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeAmniotic fluid, Chorionic villi, Peripheral blood
Container["Sterile container", "Sterile Normal Saline Container", "EDTA Vacutainer"]
Collection MethodBlood draw, Amniocentesis, Chorionic Villus Sampling

Understanding Your Results

Results from the Complete Inherited Disease Panel indicate the presence or absence of genetic mutations associated with inherited diseases, guiding clinical decisions and family planning.
📊

Positive

Genetic mutations detected, indicating risk or presence of an inherited disease. Consult a genetic counselor or healthcare provider for further evaluation and management.

📊

Negative

No mutations detected, but clinical correlation is advised. Symptoms may be due to other factors, and follow-up with a healthcare provider is recommended.

⚠️ When to Consult a Doctor:

If you experience symptoms of inherited diseases such as developmental delays, chronic pain, or seizures, or have a family history of genetic disorders, consult a healthcare provider to discuss genetic testing options.

Frequently Asked Questions

What is the cost of the Complete Inherited Disease Panel?
The cost at DNA Labs India is INR 36,000, which includes free home sample collection across India.
What symptoms indicate the need for this test?
Symptoms include developmental delays, intellectual disabilities, abnormal physical features, chronic pain, difficulty breathing, frequent infections, and seizures.
How is the test performed?
The test analyzes DNA from a blood, amniotic fluid, or chorionic villi sample using Next-Generation Sequencing (NGS) technology.
What is the turnaround time for results?
Reports are delivered in 4-6 weeks after sample collection.
Is home sample collection available?
Yes, free home sample collection is offered for online bookings across numerous cities in India.
Do I need a doctor's prescription?
Yes, a doctor's prescription is required, except for surgery, pregnancy, or travel abroad cases.
What diseases does this panel test for?
It screens for a wide range of inherited diseases by identifying genetic mutations, though specific diseases depend on the panel's design.
How accurate is the test?
The test uses advanced NGS technology for high accuracy, but results should be interpreted by a healthcare provider in clinical context.
Can insurance cover the cost?
Some insurance plans may cover genetic testing; check with your provider for eligibility.
What should I do if the test is positive?
Consult a genetic counselor or healthcare provider for further evaluation, management options, and family planning advice.
Are there any risks associated with the test?
Genetic testing is generally safe, with minimal risks such as sample collection discomfort. Discuss concerns with your healthcare provider.
How do I prepare for the test?
Obtain a doctor's prescription and follow sample collection instructions. No fasting is required unless specified.
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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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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