serw-MX  [xml]  
 


    
 Categorias DeCS

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 .
C16.320.565.618 Metal Metabolism, Inborn Errors .
C16.320.565.618.337 Hemochromatosis .
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 .
C18.452.565 Iron Metabolism Disorders .
C18.452.565.500 Iron Overload .
C18.452.565.500.480 Hemochromatosis .
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 .
C18.452.648.618 Metal Metabolism, Inborn Errors .
C18.452.648.618.337 Hemochromatosis .
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 .
D10 Lipids .
D10.390 Glycolipids .
D10.390.470 Glycosphingolipids .
D10.390.470.025 Acidic Glycosphingolipids .
D10.390.470.025.475 Gangliosides .
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 .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
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 .
1.00
 
Gangliosides .
Sialoglycosphingolipids .
0.63
 
Hemochromatosis .
Bronze Diabetes .
Bronzed Cirrhosis .
Familial Hemochromatosis .
Genetic Hemochromatosis .
Haemochromatosis .
Hemochromatoses .
Iron Storage Disorder .
Pigmentary Cirrhosis .
Primary Hemochromatosis .
Troisier-Hanot-Chauffard Syndrome .
Von Recklenhausen-Applebaum Disease .
Bronzed Cirrhoses .
Cirrhoses, Bronzed .
Cirrhoses, Pigmentary .
Cirrhosis, Bronzed .
Cirrhosis, Pigmentary .
Disease, Von Recklenhausen-Applebaum .
Diseases, Von Recklenhausen-Applebaum .
Disorder, Iron Storage .
Disorders, Iron Storage .
Familial Hemochromatoses .
Genetic Hemochromatoses .
Haemochromatoses .
Hemochromatose .
Hemochromatoses, Familial .
Hemochromatoses, Genetic .
Hemochromatosis, Familial .
Hemochromatosis, Genetic .
Iron Storage Disorders .
Pigmentary Cirrhoses .
Recklenhausen-Applebaum Disease, Von .
Recklenhausen-Applebaum Diseases, Von .
Storage Disorder, Iron .
Storage Disorders, Iron .
Syndrome, Troisier-Hanot-Chauffard .
Syndromes, Troisier-Hanot-Chauffard .
Troisier Hanot Chauffard Syndrome .
Troisier-Hanot-Chauffard Syndromes .
Von Recklenhausen Applebaum Disease .
Von Recklenhausen-Applebaum Diseases .
Diabetes, Bronze .
0.61