NIH-funded research NIH-funded research

PediCODE: consortium and biorepository for congenital diarrhea and enteropathy

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

Funded at University of California Los Angeles · NIH-11196739 · Data updated 2026-11-12

This project builds a patient network and sample bank to find genetic causes of congenital diarrhea in children.

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 year2025
Award (this year)$1,658,050
NIH project number5RC2DK118640-07
Project IDNIH-11196739 on NIH RePORTER

Who could benefit from this research

Could help

Children (typically infants and young children) with congenital or early-onset severe diarrhea or enteropathy, especially when a genetic cause is suspected and families are willing to provide clinical information and samples.

Less likely to help

Patients whose diarrhea is due to common, transient, infectious, or non-genetic causes are less likely to receive direct benefit from this program.

What this research studies

If your child has congenital or early-onset severe diarrhea, this consortium will invite you to join a multi-center patient cohort and share medical records, genetic data, and tissue samples. Collected samples will be stored in a centralized biorepository and used for genetic sequencing, single-cell RNA studies, protein-interactome analyses, and lab-grown intestinal enteroids from biopsies. The team will apply computational and imaging tools to compare patient-derived samples and search for new disease-causing genes and biological mechanisms. These resources are intended to support lab research that could lead to better diagnoses and future targeted treatments.

Why it matters

Potential benefit: Could identify the genetic cause of a child's condition, improve diagnosis, and create a foundation for targeted therapies.

How similar studies have gone: Other rare-disease biobanks and gene-discovery programs have successfully identified causal genes, though applying these methods specifically across many CoDE disorders is still relatively new.

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.