Million-Baby gene study aims to unlock secrets of genetic disease

NCT ID NCT07365254

First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study will enroll up to 1 million families to collect genetic and health information from parents and newborns. Researchers will analyze whole genomes, blood markers, and other biological data to understand how genes and environment affect pregnancy and child health. The goal is to find new ways to predict and prevent genetic diseases early in life.

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

What this could lead to

If successful, this could help identify genetic risks early in life and improve prevention of birth defects and childhood diseases.

What could go wrong

This is an observational study, not a treatment trial. It may not lead to direct medical benefits, and results may take many years to apply.

Disclaimer Read more

This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Conditions

The condition(s) this trial relates to.

hereditary disease

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • Women's Hospital, School of Medicine, Zhejiang University

    RECRUITING

    Hangzhou, Zhejiang, 310006, China