Congenital sucrase-isomaltase deficiency

MONDO:0009114

A 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

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

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