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.
Follow this condition — get notified about new trialsSub-types
Congenital sucrase-isomaltase deficiency with minimal starch tolerance
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Congenital sucrase-isomaltase deficiency without starch intolerance
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Congenital sucrase-isomaltase deficiency without sucrose intolerance
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Congenital sucrase-isomaltase deficiency with starch and lactose intolerance
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Congenital sucrase-isomaltase deficiency with starch intolerance
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Global disaccharide intolerance
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