Disorder of carbohydrate transmembrane transport and absorption
MONDO:0017706Also known as: disorder of carbohydrate absorption and transport
166 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Glucose intolerance
(130)
Encephalopathy due to GLUT1 deficiency
(5)
Congenital sucrase-isomaltase deficiency
(2)
Glucose-galactose malabsorption
(2)
Salla disease
(2)
Congenital lactase deficiency
(1)
Glucose transport disorder
(1)
Adenosine kinase deficiency
(0)
Al-Raqad syndrome
(0)
Autosomal recessive non-syndromic intellectual disability
(0)
Childhood onset GLUT1 deficiency syndrome 2
(0)
Chronic diarrhea due to glucoamylase deficiency
(0)
Congenital sucrase-isomaltase deficiency with minimal starch tolerance
(0)
Congenital sucrase-isomaltase deficiency without starch intolerance
(0)
Congenital sucrase-isomaltase deficiency without sucrose intolerance
(0)
Congenital sucrase-isomaltase deficiency with starch and lactose intolerance
(0)
Congenital sucrase-isomaltase deficiency with starch intolerance
(0)
Diarrhea-vomiting due to trehalase deficiency
(0)
Dystonia 9
(0)
Exercise-induced hyperinsulinism
(0)
Broader categories
Disease
(618)
Metabolic disease
(215)
Hereditary disease
(172)
Inborn errors of metabolism
(42)
Human disease
(14)
Carbohydrate metabolism disease
(3)
Disease of genetic or genomic mechanism
(2)
Inborn carbohydrate metabolic disorder
(2)
Disease by developmental or physiological process
(0)
Disease by etiologic mechanism
(0)