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ENSucrase-Isomaltase Deficiency, Congenital (CSID)
Alias:
Congenital Sucrase-Isomaltase Deficiency
Csid
Congenital Sucrose Intolerance
Disaccharide Intolerance
Sucrase-Isomaltase Deficiency
Disaccharide Intolerance I
Si Deficiency
Congenital Sucrose-Isomaltose Malabsorption
Csid - [congenital Sucrase-Isomaltase Deficiency]
Sucrose-Isomaltose Malabsorption, Congenital
Congenital Sucrase-Isomaltose Malabsorption
Congenital Sucrose Isomaltose Malabsorption
Intestinal Disaccharidase Deficiency
Sucrase-Alpha-Dextrinase Deficiency
Sucrose Intolerance, Congenital
Disaccharide Intolerance Type I
Sucrose Intolerance of Newborn
Disaccharide Malabsorption
Disaccharidase Deficiency
Invertase Deficiency
Sucrose Intolerance
Sucrase Deficiency
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Sucrase-Isomaltase Deficiency, Congenital, also known as congenital sucrase-isomaltase deficiency, is related to intestinal disaccharidase deficiency and diarrhea. An important gene associated with Sucrase-Isomaltase Deficiency, Congenital is SI (Sucrase-Isomaltase), and among its related pathways/superpathways are Digestion and absorption and Diseases of carbohydrate metabolism. The drugs Glycerin and Sodium citrate have been mentioned in the context of this disorder. Affiliated tissues include small intestine and colon, and related phenotypes are diarrhea and vomiting
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MALACARDS
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