Massive gene hunt launched for rare gut condition

NCT ID NCT00478712

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study aims to find the genes responsible for Hirschsprung disease, a condition where nerve cells are missing from parts of the intestine. Researchers will collect DNA samples from 3,000 people with the disease and their close family members. By analyzing common and rare genetic variations, they hope to better understand what causes the condition and why it affects some people more severely.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • New York University School of Medicine

    RECRUITING

    New York, New York, 10016, United States

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Other studies related to the condition(s) this trial covers.