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Sucrose Intolerance
Sucrose intolerance
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Topics Related to Sucrose intolerance
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Metabolic disorders
(58)
Disaccharidase
Fructose malabsorption
GSD type 0
Hereditary fructose intolerance
Hypoglycemia
Hypoglycemia
Lactose intolerance
Activated protein C resistance
Adenosine deaminase deficiency
Albinism
Alcohol flush reaction
Antithrombin III deficiency
Baker IDI Heart and Diabetes Institute
Blue diaper syndrome
Childhood obesity
Congenital disorder of glycosylation
Congenital hyperinsulinism
Crigler-Najjar syndrome
Diagnostic fast
Disorders of calcium metabolism
Ectopic calcification
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Galactosemia
Galactosemic cataract
Gangliosidosis
Gaucher's disease
Homocystinuria
Hyperglycemia
Hyperinsulinemic hypoglycemia
Hyperinsulinism
Inborn errors of metabolism
Ketotic hypoglycemia
Krabbe disease
Lipid storage disorders
List of causes of hypoglycemia
Metab-L
Methemoglobinemia
Neuronal ceroid lipofuscinosis
Niemann-Pick disease, type C
Niemann–Pick disease
Obesity
Pickardt syndrome
Pycnodysostosis
Refeeding syndrome
Richner Hanhart syndrome
Rotor syndrome
Salicylate sensitivity
Schindler disease
Selfish Brain Theory
Sitosterolemia
Stress hyperglycemia
Tay-Sachs disease
Triosephosphate isomerase deficiency
Urbach–Wiethe disease
Urea cycle disorder
Winchester syndrome
Wolman disease
more...
Symptoms
Bloating
Hypoglycemia
Inborn errors of metabolism
(107)
3 methylcrotonyl-coa carboxylase deficiency
Acatalasia
Carbamoyl phosphate synthetase I deficiency
Essential fructosuria
GSD type I
GSD type I
GSD type II
GSD type III
GSD type V
Galactose-- 1-phosphate uridylyltransferase galactosemia
Glucose-galactose malabsorption syndrome
Inborn error of metabolism
Lysinuric protein intolerance
2,4 Dienoyl-CoA reductase deficiency
2-Methylbutyryl-CoA dehydrogenase deficiency
3-hydroxy-- 3-methylglutaryl-CoA lyase deficiency
3-hydroxya- cyl-coenzyme A dehydrogenase deficiency
Acid lipase disease
Adenosine deaminase deficiency
Adenylosuccinate lyase deficiency
Aldolase A deficiency
Analbuminaemia
Arakawa's syndrome II
Argininemia
Argininosuccinic aciduria
Aspartylgl- ucosaminuria
Beta-ketothiolase deficiency
Carnitine palmitoylt- ransferase I deficiency
Carnitine palmitoylt- ransferase II deficiency
Carnitine-- acylcarnitine translocase deficiency
Cholesteryl ester storage disease
Citrullinemia
Congenital disorder of glycosylation
Crigler-Najjar syndrome
D-Glyceric acidemia
DOOR syndrome
Dihydropyrimidine dehydrogenase deficiency
Disaccharidase
Fucosidosis
Fumarase deficiency
Galactosemia
Glutaric acidemia type 2
Glutaric aciduria type 1
Glycogen storage disease
Guanidinoacetate methyltransferase deficiency
Hawkinsinuria
Hereditary fructose intolerance
Histidinemia
Holocarboxylase synthetase deficiency
Hyperlysinemia
Hypermethioninemia
Hyperprolinemia
Hypervalinemia
Idiosyncrasy
Inborn error of lipid metabolism
Isobutyryl-coenzyme A dehydrogenase deficiency
Isovaleric acidemia
Krabbe disease
Lecithin cholesterol acyltransferase deficiency
Lesch–Nyhan syndrome
Lipid storage disorder
Lipid storage disorders
Long-chain 3-hydroxya- cyl-coenzyme A dehydrogenase deficiency
Lysosomal storage disease
Lysosomal storage diseases
Malonyl-CoA decarboxylase deficiency
Maple syrup urine disease
Medium-chain acyl-coenzyme A dehydrogenase deficiency
Menkes disease
Metab-L
Methylmalonic acidemia
Methylmalonyl-CoA mutase deficiency
Mevalonate kinase deficiency
Mitochondrial trifunctional protein deficiency
Myoadenylate deaminase deficiency
N-Acetylglutamate synthase deficiency
Newborn screening
Niemann-Pick disease, type C
Organic acidemia
Ornithine transcarbamylase deficiency
Ornithine translocase deficiency
Phenylketonuria
Primary carnitine deficiency
Prolidase deficiency
Propionic acidemia
Pyruvate carboxylase deficiency
Pyruvate kinase deficiency
Refsum's disease
Rotor syndrome
Sarcosinemia
Schindler disease
Short-chain acyl-coenzyme A dehydrogenase deficiency
Sly syndrome
Smith-Lemli-Opitz syndrome
Succinic semialdehyde dehydrogenase deficiency
Tangier disease
Tetrahydrobiopterin deficiency
Trimethylaminuria
Type I tyrosinemia
Type III tyrosinemia
Tyrosinemia
Tyrosinemia type II
Urea cycle disorder
Urocanic aciduria
Very long-chain acyl-coenzyme A dehydrogenase deficiency
Wolman disease
X-linked ichthyosis
Zellweger syndrome
more...
Autosomal recessive disorders
(14)
Galactose epimerase deficiency
Cerebrotendineous xanthomatosis
Alpha-mannosidosis
GSD type I
Galactose-- 1-phosphate uridylyltransferase galactosemia
Galactose-- 1-phosphate uridylyltransferase galactosemia
GSD type V
GSD type III
GSD type II
Glucose-galactose malabsorption syndrome
Essential fructosuria
Carbamoyl phosphate synthetase I deficiency
Acatalasia
3 methylcrotonyl-coa carboxylase deficiency
Lysinuric protein intolerance
more...
Hepatology
(8)
GSD type IV
Glycogen
Hepatosplenomegaly
Gluconeogenesis
GSD type I
GSD type I
GSD type 0
GSD type III
GSD type II
more...
Genetic disorders
(18)
Hereditary disorder
GSD type I
Galactose-- 1-phosphate uridylyltransferase galactosemia
GSD type IV
GSD type V
GSD type V
GSD type III
Hereditary fructose intolerance
Galactose epimerase deficiency
GSD type II
Glucose-galactose malabsorption syndrome
Essential fructosuria
Carbamoyl phosphate synthetase I deficiency
Cerebrotendineous xanthomatosis
Acatalasia
3 methylcrotonyl-coa carboxylase deficiency
Disaccharidase
Lysinuric protein intolerance
Fructose malabsorption
more...
Gastroenterology
Lactulose
Intestinal
Bacterial overgrowth
GSD type III
Bloating
Sweeteners
Galactose metabolism
Sucrose
Fructose
Lactose
Beet sugar
Sorbitol
Disaccharides
(31)
Disaccharide
Isomaltose
2alpha-Mannobiose
3alpha-Mannobiose
Allolactose
Allolactose
Cellobiose
Gentiobiose
Isomalt
Isomaltulose
Kojibiose
Lactitol
Lactobionic acid
Lactose
Lactulose
Laminaribiose
Maltitol
Maltose
Melibiose
Neohesperidose
Nigerose
Rutinose
Sambubiose
Sophorose
Sucralfate
Sucralose
Sucrose
Sucrose acetate isobutyrate
Sucrose octaacetate
Trehalose
Turanose
Xylobiose
more...
EC 3.2.1
Lactase
Sucrase
Amylase
Invertase
Medical condition
(17)
Sucrase-isomaltase deficiency congenital
Congenital sucrose isomaltose malabsorption
Hyperuricemia
Hematologic disease
Galactose-- 1-phosphate uridylyltransferase galactosemia
Galactose-- 1-phosphate uridylyltransferase galactosemia
GSD type IV
Hereditary fructose intolerance
GSD type II
Glucose-galactose malabsorption syndrome
Essential fructosuria
Carbamoyl phosphate synthetase I deficiency
Cerebrotendineous xanthomatosis
Acatalasia
Lactose intolerance
Lysinuric protein intolerance
Inborn error of metabolism
Hypoglycemia
more...
See also
(20)
Diseases and disorders
Fructose bisphosphatase deficiency
Glycolysis
Metabolic
Aldolase B
Aldolase B
Pentose phosphate pathway
Isomaltase
Enzymes
Glucose 6-phosphatase
Fructose 1-phosphate
Gierke
Monosaccharide
Catabolism
Chemical substances
Malabsorption
Objects
Sucrase-isomaltase
Uric
Hydrogen Breath Test
Autosomal recessive
more...
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