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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

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

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Broader categories

Disease (618) Hereditary disease (172) Digestive system disorder (141) Diarrheal disease (71) 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! 2 Not yet recruiting 2 Not yet finished but already full! 1 Completed 3
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  • Massive data dive aims to improve GI care

    Knowledge-focused ENROLLING_BY_INVITATION

    This 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

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