Congenital secretory chloride diarrhea 1
MONDO:0008964Any secretory diarrhea in which the cause of the disease is a mutation in the SLC26A3 gene.
Also known as: SLC26A3 secretory diarrhea, SLC26A3 secretory diarrhoea, congenital chloridorrhea, congenital secretory chloride diarrhea type 1, congenital secretory chloride diarrhoea type 1, secretory diarrhea caused by mutation in SLC26A3, secretory diarrhoea caused by mutation in SLC26A3, CLD
10 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
-
Newborn screening study aims to catch rare diseases at birth
Diagnosis OngoingThis study offers voluntary screening for newborns in North Carolina to detect a wide range of rare health conditions early. Using a small blood sample already collected at birth, the program tests for dozens of disorders, including spinal muscular atrophy, cystic fibrosis, and m…
Sponsor: RTI International • Aim: Diagnosis
Last updated Jul 03, 2026 00:00 UTC
-
Massive data dive aims to improve GI care
Knowledge-focused ENROLLING_BY_INVITATIONThis study is a registry that will review medical records of 1,000 patients treated for benign or malignant gastrointestinal diseases between 2005 and 2030. Researchers will look at survival, symptoms like heartburn and swallowing trouble, and quality of life. The goal is to lear…
Sponsor: Methodist Health System • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:23 UTC