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Galactosemia
Galactosemia
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Related in the Kosmos
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Inborn errors of metabolism
(106)
Classic galactosemia
Essential fructosuria
GSD type I
GSD type II
GSD type III
GSD type III
GSD type V
Glycogen storage disease
Hereditary fructose intolerance
MCAD deficiency
Newborn screening
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
Acatalasia
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
Glucose-galactose malabsorption
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
Menkes disease
Metab-L
Methylmalonic acidemia
Methylmalonyl-CoA mutase deficiency
Mevalonate kinase deficiency
Mitochondrial trifunctional protein deficiency
Myoadenylate deaminase deficiency
N-Acetylglutamate synthase deficiency
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...
Metabolic disorders
(58)
GSD type 0
Gauchers disease
Homocystinuria
Activated protein C resistance
Adenosine deaminase deficiency
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
Fructose malabsorption
GM1 gangliosidoses
GM2 gangliosidoses
Galactosemic cataract
Gangliosidosis
Hereditary fructose intolerance
Hyperglycemia
Hyperinsulinemic hypoglycemia
Hyperinsulinism
Hypoglycemia
Inborn errors of metabolism
Ketotic hypoglycemia
Krabbe disease
Lactose intolerance
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
Sucrose intolerance
Tay-Sachs disease
Triosephosphate isomerase deficiency
Urbach–Wiethe disease
Urea cycle disorder
Winchester syndrome
Wolman disease
more...
Genetic disorders
(20)
Gargoylism
Gilberts syndrome
Galactokinase deficiency
Gilles de la Tourette syndrome
Galactose epimerase deficiency
Galactose epimerase deficiency
GSD type IV
Congenital adrenal hyperplasia
Inherited disease
Classic galactosemia
Gauchers disease
Phenylketonuria
GSD type V
GSD type III
GSD type I
Homocystinuria
GSD type II
Essential fructosuria
Hereditary fructose intolerance
Tyrosinemia
MCAD deficiency
more...
Medical condition
(33)
Gianotti-crosti syndrome
Epimerase deficiency
CMV disease
Udpglucose hexose-1-phosphate uridylyltransferase deficiency
Udpglucose 4-epimerase deficiency disease
Udpglucose 4-epimerase deficiency disease
Congenital hypothyroidism
Galactose-- 1-phosphate uridyl-transferase deficiency disease
Galactokinase deficiency disease
Gas gangrene
Gonococcal
Premature ovarian failure
Glomerulonephritis
Aminoaciduria
Granulomatous
Jaundice
Hemoglobinopathies
Gigantism
Giardiasis
Mental retardation
Classic galactosemia
Gargoylism
Gilberts syndrome
Gauchers disease
Gilles de la Tourette syndrome
Glycogen storage disease
Phenylketonuria
GSD type IV
Homocystinuria
Congenital adrenal hyperplasia
GSD type II
Essential fructosuria
Hereditary fructose intolerance
Tyrosinemia
more...
Autosomal recessive disorders
(15)
Classic galactosemia
Gargoylism
Gauchers disease
Galactokinase deficiency
Phenylketonuria
Phenylketonuria
Galactose epimerase deficiency
GSD type V
GSD type III
GSD type I
Homocystinuria
Congenital adrenal hyperplasia
GSD type II
Essential fructosuria
Tyrosinemia
MCAD deficiency
more...
Gastroenterology
Gastric outlet obstruction
Malabsorption
Gilberts syndrome
GSD type III
Jaundice
Diseases and disorders
Gangrenous stomatitis
Fructose bisphosphatase deficiency
Growth failure
Metabolic disorders
Gas gangrene
Aminoaciduria
Jaundice
Enzyme
Epimerase
Galactose-- 1-phosphate uridyltransferase
Galactokinase
UTP-hexose- -1-phosphate uridylyltransferase
Gamma GT
Glucosylceramidase
Symptoms
Generalized tonic clonic seizure
General ill feeling
Dysphagia
Growth failure
Mental retardation
Biochemistry
UDP-galactose
Glycolysis
Metabolize
Biochemical genetics
Causes, incidence, and risk factors
Cataract
Cirrhosis
Fatigue (medical)
Irritability
Seizure
See also
(20)
Gastrostomy tube
Galactose
Genetic code (ATGC)
Genetic imprinting
General paresis
General paresis
Galactose 1-phosphate
Gingival
Gastrointestinal perforation
Gingivectomy
Gene amplification
Gierke
PediaSure
Simple sugar
Guaiac smear test
Disaccharide
Hepatomegaly
Lactose
Gram stain
Transferase
Ascites
more...
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