serw-MX  [xml]  
 


    
 DeCS Categories

B01 Eukaryota .
B01.050 Animals .
B01.050.150 Chordata .
B01.050.150.900 Vertebrates .
B01.050.150.900.649 Mammals .
B01.050.150.900.649.313 Eutheria .
B01.050.150.900.649.313.988 Primates .
B01.050.150.900.649.313.988.700 Strepsirhini .
B01.050.150.900.649.313.988.700.572 Lorisidae .
B01.050.150.900.649.313.988.700.572.408 Galago .
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 .
C13 Female Urogenital Diseases and Pregnancy Complications .
C13.703 Pregnancy Complications .
C13.703.844 Puerperal Disorders .
C13.703.844.506 Lactation Disorders .
C13.703.844.506.389 Galactorrhea .
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 .
C17 Skin and Connective Tissue Diseases .
C17.800 Skin Diseases .
C17.800.090 Breast Diseases .
C17.800.090.937 Lactation Disorders .
C17.800.090.937.439 Galactorrhea .
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 .
D02 Organic Chemicals .
D02.033 Alcohols .
D02.033.800 Sugar Alcohols .
D02.033.800.400 Galactitol .
D09 Carbohydrates .
D09.400 Glycoconjugates .
D09.400.410 Glycolipids .
D09.400.410.209 Galactolipids .
D09.408 Glycosides .
D09.408.320 Galactosides .
D09.698 Polysaccharides .
D09.698.360 Galactans .
D09.853 Sugar Alcohols .
D09.853.400 Galactitol .
D09.947 Sugars .
D09.947.875 Monosaccharides .
D09.947.875.359 Hexoses .
D09.947.875.359.377 Galactose .
D10 Lipids .
D10.390 Glycolipids .
D10.390.355 Galactolipids .
D12 Amino Acids, Peptides, and Proteins .
D12.644 Peptides .
D12.644.400 Neuropeptides .
D12.644.400.250 Galanin .
D12.776 Proteins .
D12.776.631 Nerve Tissue Proteins .
D12.776.631.650 Neuropeptides .
D12.776.631.650.250 Galanin .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Galactitol .
Dulcitol .
A naturally occurring product of plants obtained following reduction of GALACTOSE. It appears as a white crystalline powder with a slight sweet taste. It may form in excess in the lens of the eye in GALACTOSEMIAS, a deficiency of GALACTOKINASE. .
1.00
1369
 
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. .
0.71
4314542
 
Galactans .
Polygalactoses .
Polysaccharides composed of repeating galactose units. They can consist of branched or unbranched chains in any linkages. .
0.71
102162
 
Galactolipids .
Digalactolipids .
Monogalactolipids .
A group of GLYCOLIPIDS in which the sugar group is GALACTOSE. They are distinguished from GLYCOSPHINGOLIPIDS in lacking nitrogen. They constitute the majority of MEMBRANE LIPIDS in PLANTS. .
0.67
1531
 
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. .
0.63
21788
 
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) .
0.62
291877
 
Galago .
Galagos .
Babies, Bush .
Baby, Bush .
Bush Baby .
Bush Babies .
Euoticus .
A genus of the family Lorisidae having four species which inhabit the forests and bush regions of Africa south of the Sahara and some nearby islands. The four species are G. alleni, G. crassicaudatus, G. demidovii, and G. senegalensis. There is another genus, Euoticus, containing two species which some authors have included in the Galago genus. .
0.62
 
Galanin .
Galanin (1-29) .
Galanin (1-30) .
A neuropeptide of 29-30 amino acids depending on the species. Galanin is widely distributed throughout the BRAIN; SPINAL CORD; and INTESTINES. There are various subtypes of GALANIN RECEPTORS implicating roles of galanin in regulating FOOD INTAKE; pain perception; memory; and other neuroendocrine functions. .
0.62
52696
 
Galactorrhea .
Galactorrheas .
Excessive or inappropriate LACTATION in females or males, and not necessarily related to PREGNANCY. Galactorrhea can occur either unilaterally or bilaterally, and be profuse or sparse. Its most common cause is HYPERPROLACTINEMIA. .
0.61
861501