serw-MX  [xml]  
 


    
 DeCS Categories

C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.163 Brain Diseases, Metabolic .
C10.228.140.163.100 Brain Diseases, Metabolic, Inborn .
C10.228.140.163.100.320 Galactosemias .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.320 Galactosemias .
C16.320.565.202 Carbohydrate Metabolism, Inborn Errors .
C16.320.565.202.355 Galactosemias .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.320 Galactosemias .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.320 Galactosemias .
C18.452.648.202 Carbohydrate Metabolism, Inborn Errors .
C18.452.648.202.355 Galactosemias .
D08 Enzymes and Coenzymes .
D08.811 Enzymes .
D08.811.277 Hydrolases .
D08.811.277.450 Glycoside Hydrolases .
D08.811.277.450.410 Galactosidases .
D08.811.277.450.410.100 beta-Galactosidase .
D08.811.277.450.410.100.500 Lactase .
D09 Carbohydrates .
D09.408 Glycosides .
D09.408.320 Galactosides .
D09.698 Polysaccharides .
D09.698.629 Oligosaccharides .
D09.698.629.305 Disaccharides .
D09.698.629.305.340 Lactose .
D09.947 Sugars .
D09.947.750 Disaccharides .
D09.947.750.340 Lactose .
D09.947.875 Monosaccharides .
D09.947.875.359 Hexoses .
D09.947.875.359.377 Galactose .
HP7 Homeopathic Pharmacy .
HP7.029 Homeopathic Pharmacotechniques .
HP7.029.152 Homeopathic Vehicles .
HP7.029.152.257 Lactose .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Lactase .
Lactose Galactohydrolase .
Galactohydrolase, Lactose .
An enzyme which catalyzes the hydrolysis of LACTOSE to D-GALACTOSE and D-GLUCOSE. Defects in the enzyme cause LACTOSE INTOLERANCE. .
1.00
16877
 
Galactose .
D-Galactose .
Galactopyranose .
Galactopyranoside .
D Galactose .
An aldohexose that occurs naturally in the D-form in lactose, cerebrosides, gangliosides, and mucoproteins. Deficiency of galactosyl-1-phosphate uridyltransferase (GALACTOSE-1-PHOSPHATE URIDYL-TRANSFERASE DEFICIENCY DISEASE) causes an error in galactose metabolism called GALACTOSEMIA, resulting in elevations of galactose in the blood. .
0.69
4314542
 
Lactose .
Anhydrous Lactose .
Lactose, Anhydrous .
A disaccharide of GLUCOSE and GALACTOSE in human and cow milk. It is used in pharmacy for tablets, in medicine as a nutrient, and in industry. .
0.63
14410019
 
Galactosemias .
Classic Galactosemia .
Deficiency Disease, Galactokinase .
Deficiency Disease, Galactose-1-Phosphate Uridyl-Transferase .
Deficiency Disease, UDP-Galactose-4-Epimerase .
Deficiency Disease, UDPglucose 4-Epimerase .
Epimerase Deficiency Galactosemia .
GALE Deficiency .
GALK Deficiency .
GALT Deficiency .
Galactokinase Deficiency .
Galactose Epimerase Deficiency .
Galactose-1-Phosphate Uridyltransferase Deficiency .
Galactose-1-Phosphate Uridylyltransferase Deficiency .
Galactosemia .
Galactosemia 2 .
Galactosemia 3 .
Galactosemia III .
Galactosemia, Classic .
Hereditary Galactokinase Deficiency .
UDP-Galactose-4-Epimerase Deficiency .
UDP-Galactose-4-Epimerase Deficiency Disease .
UDPGlucose Hexose-1-Phosphate Uridylyltransferase Deficiency .
UTP Hexose-1-Phosphate Uridylyltransferase Deficiency .
UTP-Hexose-1-Phosphate Uridylyltransferase Deficiency Disease .
Classic Galactosemias .
Deficiencies, GALE .
Deficiencies, GALK .
Deficiencies, GALT .
Deficiencies, Galactokinase .
Deficiencies, Galactose Epimerase .
Deficiencies, Galactose-1-Phosphate Uridyltransferase .
Deficiencies, Galactose-1-Phosphate Uridylyltransferase .
Deficiencies, Hereditary Galactokinase .
Deficiencies, UDP-Galactose-4-Epimerase .
Deficiency Disease, Galactose 1 Phosphate Uridyl Transferase .
Deficiency Disease, UDP Galactose 4 Epimerase .
Deficiency Disease, UDPglucose 4 Epimerase .
Deficiency Diseases, UDP-Galactose-4-Epimerase .
Deficiency Galactosemia, Epimerase .
Deficiency Galactosemias, Epimerase .
Deficiency, GALE .
Deficiency, GALK .
Deficiency, GALT .
Deficiency, Galactokinase .
Deficiency, Galactose Epimerase .
Deficiency, Galactose-1-Phosphate Uridyltransferase .
Deficiency, Galactose-1-Phosphate Uridylyltransferase .
Deficiency, Hereditary Galactokinase .
Deficiency, UDP-Galactose-4-Epimerase .
Epimerase Deficiency Galactosemias .
GALE Deficiencies .
GALK Deficiencies .
GALT Deficiencies .
Galactokinase Deficiencies .
Galactokinase Deficiencies, Hereditary .
Galactokinase Deficiency Diseases .
Galactokinase Deficiency, Hereditary .
Galactose 1 Phosphate Uridyl Transferase Deficiency Disease .
Galactose 1 Phosphate Uridyltransferase Deficiency .
Galactose 1 Phosphate Uridylyltransferase Deficiency .
Galactose Epimerase Deficiencies .
Galactose-1-Phosphate Uridyltransferase Deficiencies .
Galactose-1-Phosphate Uridylyltransferase Deficiencies .
Galactosemia 2s .
Galactosemia 3s .
Galactosemia IIIs .
Galactosemia, Epimerase Deficiency .
Galactosemias, Classic .
Galactosemias, Epimerase Deficiency .
Hereditary Galactokinase Deficiencies .
UDP Galactose 4 Epimerase Deficiency .
UDP Galactose 4 Epimerase Deficiency Disease .
UDP-Galactose-4-Epimerase Deficiencies .
UDP-Galactose-4-Epimerase Deficiency Diseases .
UDPGlucose Hexose 1 Phosphate Uridylyltransferase Deficiency .
UDPglucose 4 Epimerase Deficiency Disease .
UTP Hexose 1 Phosphate Uridylyltransferase Deficiency .
UTP Hexose 1 Phosphate Uridylyltransferase Deficiency Disease .
Uridyltransferase Deficiencies, Galactose-1-Phosphate .
Uridyltransferase Deficiency, Galactose-1-Phosphate .
Uridylyltransferase Deficiencies, Galactose-1-Phosphate .
Uridylyltransferase Deficiency, Galactose-1-Phosphate .
Galactokinase Deficiency Disease .
Galactose-1-Phosphate Uridyl-Transferase Deficiency Disease .
UDPglucose 4-Epimerase Deficiency Disease .
UDPglucose-Hexose-1-Phosphate Uridylyltransferase Deficiency .
UDPglucose Hexose-1-Phosphate Uridylyltransferase Deficiency .
GALACTOSEMIA .
A group of inherited enzyme deficiencies which feature elevations of GALACTOSE in the blood. This condition may be associated with deficiencies of GALACTOKINASE; UDPGLUCOSE-HEXOSE-1-PHOSPHATE URIDYLYLTRANSFERASE; or UDPGLUCOSE 4-EPIMERASE. The classic form is caused by UDPglucose-Hexose-1-Phosphate Uridylyltransferase deficiency, and presents in infancy with FAILURE TO THRIVE; VOMITING; and INTRACRANIAL HYPERTENSION. Affected individuals also may develop MENTAL RETARDATION; JAUNDICE; hepatosplenomegaly; ovarian failure (PRIMARY OVARIAN INSUFFICIENCY); and cataracts. (From Menkes, Textbook of Child Neurology, 5th ed, pp61-3) .
0.61
291877
 
Galactosidases .
Galactosidase .
A family of galactoside hydrolases that hydrolyze compounds with an O-galactosyl linkage. EC 3.2.1.-. .
0.58
95032
 
Galactosides .
Glycosides formed by the reaction of the hydroxyl group on the anomeric carbon atom of galactose with an alcohol to form an acetal. They include both alpha- and beta-galactosides. .
0.58
21788