Non-invasive Prenatal Test - Basic (NIPT - Basic)

₱ 24,000₱ 30,000

The Non-Invasive Prenatal Test (NIPT – Basic) uses a simple blood sample from the mother to screen for common chromosomal conditions, including Trisomy 21 (Down syndrome), Trisomy 18, Trisomy 13, and sex chromosome aneuploidies like Turner and Klinefelter syndromes. It also includes fetal gender determination and may report incidental chromosomal findings.

Safe, highly accurate, and available as early as 10 weeks into pregnancy, NIPT – Basic empowers expectant parents with early, reliable insights.

Additional Information

Test Requirements

A medical professional will collect a blood sample from the expecting mother at our partner clinic, which will then be sent to our partner clinic's laboratory for analysis. Once the test is complete, the results will be securely emailed to the registered client.

Turn around time

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Frequently Asked Questions

What is Hati Health?

Hati Health is your digital health companion that connects you with trusted clinics and doctors across the Philippines. We make booking appointments and accessing healthcare simple and convenient, all through our growing network of 100+ partners.

What are the participating clinics and locations?

We work with a growing network of trusted clinics nationwide, making it convenient to find quality care wherever you are. Just share what service you need and your location—we'll show you all the available options nearby.

What are your payment options?

We offer flexible payment options including GCash, credit/debit cards, and bank transfers, with installment plans through BillEase and GoTyme. While we don't accept insurance yet, our affordable prices are often lower than HMO networks, and we're working on future partnerships.

How do I contact Hati Health?

You can reach us through our support chat on the website, Messenger or email us at [email protected]. Our team is here to assist you.

More About This Product

Find best NIPT - Basic price in the Philippines. LablogDNA NIPT - Basic is a non-invasive prenatal test that screens for common chromosomal conditions using a simple maternal blood sample. This test effectively detects Trisomy 21 (Down syndrome), Trisomy 18 (Edwards syndrome), and Trisomy 13 (Patau syndrome), alongside Sex Chromosome Aneuploidies such as Turner syndrome and Klinefelter syndrome. A key benefit of LablogDNA NIPT - Basic is that it includes fetal gender determination, offering parents valuable insights during early pregnancy. This test can be performed as early as the 10th week of pregnancy, making it an ideal choice for expectant parents who seek early and accurate results. With a focus on safety and precision, LablogDNA NIPT - Basic aids in informed decision-making, especially for parents facing potential complications like ovarian cysts, hormonal imbalances, and missed periods. Overall, this prenatal test is an essential resource for ensuring maternal and fetal health.