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Congenital secretory sodium diarrhea 3

MONDO:0010036

Any secretory diarrhea in which the cause of the disease is a mutation in the SPINT2 gene.

Also known as: SPINT2 secretory diarrhea, SPINT2 secretory diarrhoea, congenital secretory sodium diarrhea type 3, congenital secretory sodium diarrhoea type 3, secretory diarrhea caused by mutation in SPINT2, secretory diarrhoea caused by mutation in SPINT2, DIAR3, diarrhea 3, secretory sodium, congenital, syndromic

3 clinical trials for this condition and its sub-types.

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Broader categories

Disease (680) Hereditary disease (176) Digestive system disorder (160) Diarrheal disease (74) Human disease (14) Disease of genetic or genomic mechanism (2) Congenital diarrhea (0) Congenital secretory diarrhea (0) Congenital sodium diarrhea (0) Disease by body system or component (0)
Trials to join now! 1 Not yet recruiting 1 Completed 1
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  • Could postbiotics soothe diarrhea? small trial tests new supplement

    Symptom relief Completed

    This completed pilot trial tested two postbiotic supplements (ABB S3 and ABB C22) in 100 hospitalized patients with diarrhea or gut symptoms from tube feeding. The goal was to see if these nutritional supplements could ease symptoms like diarrhea, vomiting, and improve stool cons…

    Phase: NA • Sponsor: AB Biotek • Aim: Symptom relief

    Last updated Jun 27, 2026 07:53 UTC

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