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 .
C10.228.140.163.100.435.825.300.300 Gangliosidoses, GM2 .
C10.228.140.163.100.435.825.300.300.500 Tay-Sachs Disease .
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 .
C16.320.565.189.435.825.300.300 Gangliosidoses, GM2 .
C16.320.565.189.435.825.300.300.500 Tay-Sachs Disease .
C16.320.565.202 Carbohydrate Metabolism, Inborn Errors .
C16.320.565.202.251 Fructose Metabolism, Inborn Errors .
C16.320.565.202.251.221 Fructose-1,6-Diphosphatase Deficiency .
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 .
C16.320.565.398.641.803.350.300 Gangliosidoses, GM2 .
C16.320.565.398.641.803.350.300.850 Tay-Sachs Disease .
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 .
C16.320.565.595.554.825.300.300 Gangliosidoses, GM2 .
C16.320.565.595.554.825.300.300.840 Tay-Sachs Disease .
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 .
C18.452.132.100.435.825.300.300 Gangliosidoses, GM2 .
C18.452.132.100.435.825.300.300.500 Tay-Sachs Disease .
C18.452.584 Lipid Metabolism Disorders .
C18.452.584.687 Lipidoses .
C18.452.584.687.803 Sphingolipidoses .
C18.452.584.687.803.350 Gangliosidoses .
C18.452.584.687.803.350.300 Gangliosidoses, GM2 .
C18.452.584.687.803.350.300.850 Tay-Sachs Disease .
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 .
C18.452.648.189.435.825.300.300 Gangliosidoses, GM2 .
C18.452.648.189.435.825.300.300.500 Tay-Sachs Disease .
C18.452.648.202 Carbohydrate Metabolism, Inborn Errors .
C18.452.648.202.251 Fructose Metabolism, Inborn Errors .
C18.452.648.202.251.221 Fructose-1,6-Diphosphatase Deficiency .
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 .
C18.452.648.398.641.803.350.300 Gangliosidoses, GM2 .
C18.452.648.398.641.803.350.300.850 Tay-Sachs Disease .
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 .
C18.452.648.595.554.825.300.300 Gangliosidoses, GM2 .
C18.452.648.595.554.825.300.300.840 Tay-Sachs Disease .
D08 Enzymes and Coenzymes .
D08.811 Enzymes .
D08.811.277 Hydrolases .
D08.811.277.352 Esterases .
D08.811.277.352.650 Phosphoric Monoester Hydrolases .
D08.811.277.352.650.200 Fructose-Bisphosphatase .
D09 Carbohydrates .
D09.894 Sugar Phosphates .
D09.894.417 Hexosephosphates .
D09.894.417.592 Hexosediphosphates .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
Fructose-1,6-Diphosphatase Deficiency .
Deficiency, Hexosediphosphatase .
Fructose 1,6 Diphosphatase Deficiency .
Fructosediphosphatase Deficiency .
Deficiencies, Fructose-1,6-Bisphosphatase .
Deficiencies, Fructose-1,6-Diphosphatase .
Deficiencies, Fructose-Biphosphatase .
Deficiencies, Fructosediphosphatase .
Deficiencies, Hexosediphosphatase .
Deficiency, Fructose-1,6-Bisphosphatase .
Deficiency, Fructose-1,6-Diphosphatase .
Deficiency, Fructose-Biphosphatase .
Deficiency, Fructosediphosphatase .
Fructose 1,6 Bisphosphatase Deficiency .
Fructose Biphosphatase Deficiency .
Fructose-1,6-Bisphosphatase Deficiencies .
Fructose-1,6-Diphosphatase Deficiencies .
Fructose-Biphosphatase Deficiencies .
Fructosediphosphatase Deficiencies .
Hexosediphosphatase Deficiencies .
Fructose-1,6-Bisphosphatase Deficiency .
Hexosediphosphatase Deficiency .
Fructose-Biphosphatase Deficiency .
1.00
 
Fructose-Bisphosphatase .
D-Fructose-1,6-Bisphosphate 1-Phosphohydrolase .
FDPase .
Fructose-1,6-Biphosphatase .
1-Phosphohydrolase, D-Fructose-1,6-Bisphosphate .
D Fructose 1,6 Bisphosphate 1 Phosphohydrolase .
Fructose 1,6 Biphosphatase .
Fructose 1,6 Bisphosphatase .
Fructose 1,6 Diphosphatase .
Fructose Bisphosphatase .
Fructose-1,6-Bisphosphatase .
Fructosediphosphatase .
Hexosediphosphatase .
Fructose-1,6-Diphosphatase .
0.80
 
Hexosediphosphates .
0.73
 
Tay-Sachs Disease .
Amaurotic Familial Idiocy .
B Variant GM2 Gangliosidosis .
B Variant GM2-Gangliosidosis .
Deficiency Disease Hexosaminidase A .
Familial Amaurotic Idiocy .
GM2 Gangliosidosis, B Variant .
GM2 Gangliosidosis, Type 1 .
GM2 Gangliosidosis, Type I .
GM2-Gangliosidosis, Type I .
Gangliosidosis GM2 , Type 1 .
Gangliosidosis GM2, Type I .
HexA Deficiency .
Hexosaminidase A Deficiency .
Hexosaminidase alpha-Subunit Deficiency (Variant B) .
Sphingolipidosis, Tay-Sachs .
Amaurotic Idiocy, Familial .
B Variant GM2-Gangliosidoses .
Deficiency, Hexosaminidase A .
Deficiency, Hexosaminidase alpha-Subunit (Variant B) .
GM2-Gangliosidosis, B Variant .
Hexosaminidase alpha Subunit Deficiency (Variant B) .
Sphingolipidosis, Tay Sachs .
Tay Sachs Disease .
Tay Sachs Disease, B Variant .
Tay-Sachs Sphingolipidosis .
Type I GM2-Gangliosidosis .
Gangliosidosis G(M2), Type I .
G(M2) Gangliosidosis, Type I .
Gangliosidosis GM2, B Variant .
Hexosaminidase A Deficiency Disease .
Tay-Sachs Disease, B Variant .
Amaurotic Familial Idiocy .
Gangliosidosis GM2, Type I .
0.70