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Fructose Intolerance
Fructose intolerance
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Metabolic disorders
(59)
Fructose malabsorption
GSD type 0
Galactosemia
Inborn errors of metabolism
Lactose intolerance
Lactose intolerance
Niemann Pick disease
Sucrose 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
Disaccharidase
Disorders of calcium metabolism
Ectopic calcification
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Galactosemic cataract
Gangliosidosis
Gaucher's disease
Homocystinuria
Hyperglycemia
Hyperinsulinemic hypoglycemia
Hyperinsulinism
Hypoglycemia
Ketotic hypoglycemia
Krabbe disease
Lipid storage disorders
List of causes of hypoglycemia
Metab-L
Methemoglobinemia
Neuronal ceroid lipofuscinosis
Niemann-Pick disease, type C
Obesity
Obesogen
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...
Inborn errors of metabolism
(106)
Acatalasia
Essential fructosuria
GSD type I
GSD type II
GSD type III
GSD type III
GSD type V
Galactose-- 1-phosphate uridylyltransferase galactosemia
Glucose-galactose malabsorption
Glycogen storage disease
Methylmalonic acidemia
Phenylketonuria
Tyrosinemia
2,4 Dienoyl-CoA reductase deficiency
2-Methylbutyryl-CoA dehydrogenase deficiency
3-Methylcr- otonyl-CoA carboxylase 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
Carbamoyl phosphate synthetase I 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
Guanidinoacetate methyltransferase deficiency
Hawkinsinuria
Histidinemia
Holocarboxylase synthetase deficiency
Hyperlysinemia
Hypermethioninemia
Hyperprolinemia
Hypervalinemia
Idiosyncrasy
Inborn error of lipid metabolism
Inborn error of 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
Lysinuric protein intolerance
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
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
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 type II
Urea cycle disorder
Urocanic aciduria
Very long-chain acyl-coenzyme A dehydrogenase deficiency
Wolman disease
X-linked ichthyosis
Zellweger syndrome
more...
Genetic disorders
(22)
Cystinosis
Fibromuscular dysplasia
GSD type IV
Dubin-Johnson syndrome
Galactose epimerase deficiency
Galactose epimerase deficiency
Familial paroxysmal polyserositis
Acrodermatitis enteropathica
Cystathioninuria
Fructose malabsorption
GSD type I
Galactose-- 1-phosphate uridylyltransferase galactosemia
Tyrosinemia
Galactosemia
Essential fructosuria
GSD type V
Methylmalonic acidemia
GSD type III
GSD type II
Niemann Pick disease
Phenylketonuria
Glucose-galactose malabsorption
Acatalasia
more...
Diseases and disorders
(34)
Focal segmental glomerulosclerosis
Hemorrhagic thrombocythemia
Frambesia
Intraparenchymal hemorrhage
Hand-Schul- ler-Christian disease
Hand-Schul- ler-Christian disease
Haverhill fever
Hansens Disease
Hereditary amyloidosis
Hemangioma
Funnel chest
Fox Fordyce disease
Hageman factor
Fungal infection
Fructose bisphosphatase deficiency
Renal tubular acidosis
Hereditary-sensory and autonomic neuropathy type iii
Reactive hypoglycemia
Glycogen storage disease
Cystinosis
Galactose-- 1-phosphate uridylyltransferase galactosemia
Tyrosinemia
Galactosemia
Essential fructosuria
Methylmalonic acidemia
Fibromuscular dysplasia
Lactose intolerance
GSD type IV
Familial paroxysmal polyserositis
GSD type II
Acrodermatitis enteropathica
Niemann Pick disease
Phenylketonuria
Glucose-galactose malabsorption
Acatalasia
more...
Kidney diseases
Fanconi syndrome
Focal segmental glomerulosclerosis
Renal tubular acidosis
Fibromuscular dysplasia
Carbohydrates
Highly conserved sequence
Monosaccharides
Monosaccharide
Glycolysis
Gluconeogenesis
Hepatology
(12)
Hepatic transplant
Hepatosplenomegaly
Hepatomegaly
Glycogenolysis
Glycogen storage disease
Glycogen storage disease
GSD type I
GSD type 0
GSD type IV
GSD type III
Dubin-Johnson syndrome
GSD type II
Gluconeogenesis
more...
Sweeteners
Fructose
Galactose metabolism
Sucrose
Sorbitol
Metabolic pathways
(29)
Pentose phosphate pathway
Alanine cycle
Alpha oxidation
Alpha-aminoadipate pathway
Aminoshikimate pathway
Aminoshikimate pathway
Beta oxidation
Citric acid cycle
Cori cycle
Entner–Doudoroff pathway
Gluconeogenesis
Glucose cycle
Glycogenesis
Glycogenolysis
Glycolysis
Glyoxylate cycle
Kynurenine pathway
Lactic acid fermentation
Mevalonate inhibition
Mevalonate pathway
Microsomal Ethanol Oxidizing System
Non-mevalonate pathway
Octadecanoid pathway
Polyol pathway
Reductive acetyl-CoA pathway
Reverse Krebs cycle
Steroid
Transsulfuration pathway
Urea Cycle
Urea cycle
more...
Lysosomal storage diseases
(40)
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Batten disease
Canavan disease
Cholesteryl ester storage disease
Cholesteryl ester storage disease
Cystinosis
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
GSD type II
Galactosialidosis
Gangliosidosis
Gaucher's disease
Glycoproteinosis
Hunter syndrome
Hurler syndrome
I-cell disease
Krabbe disease
Lipid storage disorder
Lysosomal storage disease
Metachromatic leukodystrophy
Morquio syndrome
Mucolipidosis
Mucolipidosis type IV
Mucopolysa- ccharidosis
Multiple sulfatase deficiency
Neuronal ceroid lipofuscinosis
Niemann Pick disease
Niemann-Pick disease, type C
Pseudo-Hurler polydystrophy
Pycnodysostosis
Salla disease
Sandhoff disease
Sanfilippo syndrome
Schindler disease
Sialidosis
Sly syndrome
Tay-Sachs disease
Wolman disease
more...
Symptoms
(9)
Foul smelling stools
Fullness after eating
Convulsion
Irritability
Jaundice
Jaundice
Vomiting
Skeletal deformities
Sucrose intolerance
Galactosemia
more...
Biochemistry
Aldolase
Fructans
Alpha-aminoadipic acid
Fructose 1-phosphate
Glycolysis
Gluconeogenesis
Signs and tests
Liver biopsy
Liver function tests
Renal function
Uric acid blood test
Hepatosplenomegaly
See also
(20)
Frenectomy
Foot disorders
Folacin
Herniation of the brain
Heart sounds
Heart sounds
Fungus ball
Fuchs dystrophy
Harrington rod
Fungal keratitis
Aldolase B
Glucose 6-phosphatase
Actidose-Aqua
Food intolerance
Calpol
Gierke
Fructose 1-phosphate
Chemical substances
Ethyl parahydroxybenzoate
Disaccharide
Costal margin
more...
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