Congenital sucrase-isomaltase deficiency
MONDO:0009114A disorder of carbohydrate absorption and transport caused by autosomal recessive mutation of the SI gene, characterized by malabsorption of sucrose and maltose.
Also known as: CSID, congenital sucrase-isomaltase deficiency, congenital sucrose intolerance, disaccharide intolerance, genetic sucrase-isomaltose malabsorption, sucrase-isomaltase deficiency, SI deficiency, congenital sucrose malabsorption
3 clinical trials for this condition and its sub-types.
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Broader categories
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AI stethoscope aims to spot hidden heart and lung problems in children
Diagnosis Recruiting nowThis trial is developing an AI-powered device that listens to children's heart, breath, and bowel sounds to identify signs of common diseases like congenital heart disease, bronchopneumonia, and abdominal issues. It will involve 30,000 children aged 0-18, some with these conditio…
Sponsor: Xinhua Hospital, Shanghai Jiao Tong University School of Medicine • Aim: Diagnosis
Last updated Aug 14, 2026 00:00 UTC
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IBS study: does weak starch digestion spike gut troubles?
Knowledge-focused Recruiting nowThis study looks at people with Irritable Bowel Syndrome (IBS) who have a reduced ability to break down starch and sugar due to low enzyme levels. Researchers want to see if these individuals have a smaller rise in blood sugar after a meal and more bowel symptoms compared to thos…
Phase: NA • Sponsor: Region Skane • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:24 UTC