serw-MX  [xml]  
 


    
 DeCS Categories

C07 Stomatognathic Diseases .
C07.465 Mouth Diseases .
C07.465.815 Salivary Gland Diseases .
C07.465.815.929 Xerostomia .
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 .
C10.228.140.163.100.435 Lysosomal Storage Diseases, Nervous System .
C10.228.140.163.100.435.825 Sphingolipidoses .
C10.228.140.163.100.435.825.300 Gangliosidoses .
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 .
C16.320.565.189.435 Lysosomal Storage Diseases, Nervous System .
C16.320.565.189.435.825 Sphingolipidoses .
C16.320.565.189.435.825.300 Gangliosidoses .
C16.320.565.398 Lipid Metabolism, Inborn Errors .
C16.320.565.398.641 Lipidoses .
C16.320.565.398.641.803 Sphingolipidoses .
C16.320.565.398.641.803.350 Gangliosidoses .
C16.320.565.595 Lysosomal Storage Diseases .
C16.320.565.595.554 Lysosomal Storage Diseases, Nervous System .
C16.320.565.595.554.825 Sphingolipidoses .
C16.320.565.595.554.825.300 Gangliosidoses .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.435 Lysosomal Storage Diseases, Nervous System .
C18.452.132.100.435.825 Sphingolipidoses .
C18.452.132.100.435.825.300 Gangliosidoses .
C18.452.584 Lipid Metabolism Disorders .
C18.452.584.687 Lipidoses .
C18.452.584.687.803 Sphingolipidoses .
C18.452.584.687.803.350 Gangliosidoses .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.435 Lysosomal Storage Diseases, Nervous System .
C18.452.648.189.435.825 Sphingolipidoses .
C18.452.648.189.435.825.300 Gangliosidoses .
C18.452.648.398 Lipid Metabolism, Inborn Errors .
C18.452.648.398.641 Lipidoses .
C18.452.648.398.641.803 Sphingolipidoses .
C18.452.648.398.641.803.350 Gangliosidoses .
C18.452.648.595 Lysosomal Storage Diseases .
C18.452.648.595.554 Lysosomal Storage Diseases, Nervous System .
C18.452.648.595.554.825 Sphingolipidoses .
C18.452.648.595.554.825.300 Gangliosidoses .
D09 Carbohydrates .
D09.400 Glycoconjugates .
D09.400.410 Glycolipids .
D09.400.410.420 Glycosphingolipids .
D09.400.410.420.025 Acidic Glycosphingolipids .
D09.400.410.420.025.475 Gangliosides .
D09.400.410.420.025.475.390 G(M1) Ganglioside .
D10 Lipids .
D10.390 Glycolipids .
D10.390.470 Glycosphingolipids .
D10.390.470.025 Acidic Glycosphingolipids .
D10.390.470.025.475 Gangliosides .
D10.390.470.025.475.390 G(M1) Ganglioside .
D10.570 Membrane Lipids .
D10.570.877 Sphingolipids .
D10.570.877.360 Glycosphingolipids .
D10.570.877.360.025 Acidic Glycosphingolipids .
D10.570.877.360.025.475 Gangliosides .
D10.570.877.360.025.475.390 G(M1) Ganglioside .
M01 Persons .
M01.686 Population Groups .
M01.686.508 Continental Population Groups .
M01.686.508.200 Asian Continental Ancestry Group .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Glycosphingolipids .
Asialogangliosides .
Sphingoglycolipids .
Lipids containing at least one monosaccharide residue and either a sphingoid or a ceramide (CERAMIDES). They are subdivided into NEUTRAL GLYCOSPHINGOLIPIDS comprising monoglycosyl- and oligoglycosylsphingoids and monoglycosyl- and oligoglycosylceramides; and ACIDIC GLYCOSPHINGOLIPIDS which comprises sialosylglycosylsphingolipids (GANGLIOSIDES); SULFOGLYCOSPHINGOLIPIDS (formerly known as sulfatides), glycuronoglycosphingolipids, and phospho- and phosphonoglycosphingolipids. (From IUPAC's webpage) .
1.00
213941
 
Gangliosides .
Sialoglycosphingolipids .
A subclass of ACIDIC GLYCOSPHINGOLIPIDS. They contain one or more sialic acid (N-ACETYLNEURAMINIC ACID) residues. Using the Svennerholm system of abbrevations, gangliosides are designated G for ganglioside, plus subscript M, D, or T for mono-, di-, or trisialo, respectively, the subscript letter being followed by a subscript arabic numeral to indicated sequence of migration in thin-layer chromatograms. (From Oxford Dictionary of Biochemistry and Molecular Biology, 1997) .
0.60
669016
 
G(M1) Ganglioside .
GM1a Monosialoganglioside .
Ceramide, Monosialosyl Tetraglycosyl .
Monosialoganglioside, GM1a .
Tetraglycosyl Ceramide, Monosialosyl .
Monosialosyl Tetraglycosyl Ceramide .
A specific monosialoganglioside that accumulates abnormally within the nervous system due to a deficiency of GM1-b-galactosidase, resulting in GM1 gangliosidosis. .
0.58
183831
 
Xerostomia .
Asialias .
Dryness, Mouth .
Hyposalivations .
Xerostomias .
Asialia .
Hyposalivation .
Mouth Dryness .
Decreased salivary flow. .
0.51
2494305
 
Asian Continental Ancestry Group .
Asians .
Asiatic Race .
Burmese .
Cambodians .
Chinese .
Japanese .
Koreans .
Mongoloid Race .
Thai 26058 .
Vietnamese .
Asian .
Asiatic Races .
Burmeses .
Cambodian .
Mongoloid Races .
Race, Asiatic .
Race, Mongoloid .
Races, Asiatic .
Races, Mongoloid .
Thaus .
Vietnameses .
Asiatic Race .
Mongoloid Race .
Individuals whose ancestral origins are in the southeastern and eastern areas of the Asian continent. .
0.50
11451219
 
Gangliosidoses .
Ganglioside Storage Diseases .
Ganglioside Storage Disorders .
Gangliosidosis .
Ganglioside Storage Disease .
Ganglioside Storage Disorder .
Storage Disease, Ganglioside .
Storage Diseases, Ganglioside .
Storage Disorder, Ganglioside .
Storage Disorders, Ganglioside .
A group of autosomal recessive lysosomal storage disorders marked by the accumulation of GANGLIOSIDES. They are caused by impaired enzymes or defective cofactors required for normal ganglioside degradation in the LYSOSOMES. Gangliosidoses are classified by the specific ganglioside accumulated in the defective degradation pathway. .
0.49
9568