NIH-funded research NIH-funded research

Understanding rare genetic causes of congenital diarrhea in children

Official title: COngenital Diarrhea and Enteropathy (PediCODE) Consortium and BioRepository

Funded at University of California Los Angeles · NIH-10978459 · Data updated 2026-11-12

This study is looking for the genetic reasons behind congenital diarrhea and enteropathy in kids under 11, so if your child has this condition, researchers want to gather information and samples to help find better ways to understand and diagnose these rare disorders.

More Diarrhea research and trials

Quick facts

Grant typeNIH-funded research
Study typeNIH-funded research
Funding institutionUniversity of California Los Angeles
NIH-funded
Lab location1 site (Los Angeles, United States)
Project startSeptember 15, 2019
Project endAugust 31, 2029
Funding year2024
Award (this year)$2,000,000
NIH project number2RC2DK118640-06
Project IDNIH-10978459 on NIH RePORTER

Who could benefit from this research

Could help

Ideal candidates for this research are children under 11 years old diagnosed with congenital diarrhea or enteropathy.

Less likely to help

Patients with non-genetic causes of diarrhea or those over the age of 11 may not benefit from this research.

What this research studies

This research focuses on identifying the genetic causes of congenital diarrhea and enteropathy (CoDE) in children under 11 years old. By creating a consortium and biorepository, the project aims to collect clinical data and biological samples from affected patients. This will help researchers understand the clinical features and underlying mechanisms of these rare disorders. The study involves a multidisciplinary team of physician-scientists who will analyze patient samples to uncover genetic information and develop new diagnostic tools.

Why it matters

Potential benefit: If successful, this research could lead to better diagnosis and management of congenital diarrhea disorders in children.

How similar studies have gone: Previous research has shown promise in identifying genetic causes of rare disorders, indicating potential success for this approach.

Where this research is happening

  • University of California Los Angeles
    Los Angeles, United States
    Active

Researchers

  • Principal investigator: Martin, Martin G — University of California Los Angeles
  • Study coordinator: Martin, Martin G

Related research

Other NIH-funded projects on the same topics.

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.