Congenital sucrase-isomaltase deficiency
From BugSigDB
A disorder of carbohydrate absorption and transport caused by autosomal recessive mutation of the SI gene, characterised by malabsorption of sucrose and maltose.
- Aliases
- congenital sucrase-isomaltase deficiency
- Congenital sucrase-isomaltose malabsorption
- congenital sucrase-isomaltose malabsorption
- Congenital sucrose intolerance
- congenital sucrose intolerance
- congenital sucrose malabsorption
- congenital sucrose-isomaltase intolerance
- congenital sucrose-isomaltase malabsorption
- CSID
- Disaccharide intolerance
- disaccharide intolerance
- disaccharide intolerance 1
- disaccharide intolerance i
- disaccharide intolerance, 1
- genetic sucrase-isomaltose malabsorption
- intestinal sucrase-a-dextrinase deficiency
- invertase deficiency
- SI deficiency
- sucrase-alpha-dextrinase deficiency
- sucrase-isomaltase deficiency
- Sucrase-isomaltase deficiency, congenital
- sucrase-isomaltase deficiency, congenital
- sucrose intolerance congenital
- sucrose intolerance, congenital
- sucrose isomaltose enzyme deficiency
- sucrose-isomaltase malabsorption, congenital
- sucrose-isomaltose malabsorption, congenital
