Cure My Disease

Don't miss your cure!

Home News Browse Soon ready About
Log in / Sign up

Browse

Explore conditions, clinical trials, and the organisations running them.

Conditions By category Trials Sponsors

← All categories

Up to: Disorder of carbohydrate transmembrane transport and absorption · Intestinal disaccharidase deficiency

Congenital sucrase-isomaltase deficiency

A disorder of carbohydrate absorption and transport caused by autosomal recessive mutation of the SI gene, characterized by malabsorption of sucrose and maltose.

2 trials tagged with this condition →

  • Congenital sucrase-isomaltase deficiency with minimal starch tolerance 0 trials
  • Congenital sucrase-isomaltase deficiency with starch and lactose intolerance 0 trials
  • Congenital sucrase-isomaltase deficiency with starch intolerance 0 trials
  • Congenital sucrase-isomaltase deficiency without starch intolerance 0 trials
  • Congenital sucrase-isomaltase deficiency without sucrose intolerance 0 trials
  • Global disaccharide intolerance 0 trials

Cure My Disease

Helping patients find clinical trials that match their disease.

Why was Cure my disease built?

Explore

Home News Browse Glossary About Terms of use Contact us

This is a site from Cyber and Space