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 .
C10.228.140.163.100.435.340 Glycogen Storage Disease Type II .
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 .
C16.320.565.189.435.340 Glycogen Storage Disease Type II .
C16.320.565.202 Carbohydrate Metabolism, Inborn Errors .
C16.320.565.202.449 Glycogen Storage Disease .
C16.320.565.202.449.500 Glycogen Storage Disease Type II .
C16.320.565.202.449.520 Glycogen Storage Disease Type III .
C16.320.565.595 Lysosomal Storage Diseases .
C16.320.565.595.554 Lysosomal Storage Diseases, Nervous System .
C16.320.565.595.554.340 Glycogen Storage Disease Type II .
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 .
C18.452.132.100.435.340 Glycogen Storage Disease Type II .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.435 Lysosomal Storage Diseases, Nervous System .
C18.452.648.189.435.340 Glycogen Storage Disease Type II .
C18.452.648.202 Carbohydrate Metabolism, Inborn Errors .
C18.452.648.202.449 Glycogen Storage Disease .
C18.452.648.202.449.500 Glycogen Storage Disease Type II .
C18.452.648.202.449.520 Glycogen Storage Disease Type III .
C18.452.648.595 Lysosomal Storage Diseases .
C18.452.648.595.554 Lysosomal Storage Diseases, Nervous System .
C18.452.648.595.554.340 Glycogen Storage Disease Type II .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
Glycogen Storage Disease Type III .
Amylo-1,6-Glucosidase Deficiency .
Cori Disease .
Deficiency, Debrancher .
Glycogen Debrancher Deficiency .
Glycogen Storage Disease III .
Glycogen Storage Disease Type 3 .
Amylo 1,6 Glucosidase Deficiency .
Amylo-1,6-Glucosidase Deficiencies .
Coris Disease .
Debrancher Deficiencies .
Debrancher Deficiencies, Glycogen .
Debrancher Deficiency, Glycogen .
Deficiencies, Amylo-1,6-Glucosidase .
Deficiencies, Debrancher .
Deficiencies, Glycogen Debrancher .
Deficiency, Amylo-1,6-Glucosidase .
Deficiency, Glycogen Debrancher .
Dextrinoses, Limit .
Dextrinosis, Limit .
Disease, Cori .
Disease, Cori's .
Disease, Forbes .
Glycogen Debrancher Deficiencies .
Glycogenosis 3s .
Limit Dextrinoses .
Cori's Disease .
Debrancher Deficiency .
Forbes Disease .
Glycogen Debranching Enzyme Deficiency .
Glycogenosis 3 .
Limit Dextrinosis .
1.00
 
Glycogen Storage Disease Type II .
Acid Alpha-Glucosidase Deficiency .
Acid Maltase Deficiency .
Adult Glycogen Storage Disease Type II .
Alpha-1,4-Glucosidase Deficiency .
Deficiency Disease, Acid Maltase .
Deficiency Disease, Lysosomal alpha-1,4-Glucosidase .
Deficiency of Alpha-Glucosidase .
GAA Deficiency .
GSD II .
GSD2 13663 .
Glycogen Storage Disease II .
Glycogen Storage Disease Type 2 .
Glycogen Storage Disease Type II, Adult .
Glycogen Storage Disease Type II, Infantile .
Glycogen Storage Disease Type II, Juvenile .
Glycogenosis Type II .
Infantile Glycogen Storage Disease Type II .
Juvenile Glycogen Storage Disease Type II .
Pompe's Disease .
Acid Alpha Glucosidase Deficiency .
Acid Alpha-Glucosidase Deficiencies .
Acid Maltase Deficiencies .
Alpha 1,4 Glucosidase Deficiency .
Alpha-1,4-Glucosidase Deficiencies .
Alpha-Glucosidase Deficiencies .
Alpha-Glucosidase Deficiencies, Acid .
Alpha-Glucosidase Deficiency .
Alpha-Glucosidase Deficiency, Acid .
Deficiencies, Acid Alpha-Glucosidase .
Deficiencies, Acid Maltase .
Deficiencies, Alpha-1,4-Glucosidase .
Deficiencies, GAA .
Deficiency of Alpha Glucosidase .
Deficiency, Acid Alpha-Glucosidase .
Deficiency, Acid Maltase .
Deficiency, Alpha-1,4-Glucosidase .
Deficiency, GAA .
Disease, Pompe .
Disease, Pompe's .
GAA Deficiencies .
GSD2s .
Generalized Glycogenoses .
Glycogenoses, Generalized .
Glycogenosis, Generalized .
Lysosomal alpha 1,4 Glucosidase Deficiency Disease .
Maltase Deficiencies, Acid .
Pompes Disease .
Type II, Glycogenosis .
Type IIs, Glycogenosis .
Generalized Glycogenosis .
Glycogenosis 2 .
Pompe Disease .
Acid Maltase Deficiency Disease .
Lysosomal alpha-1,4-Glucosidase Deficiency Disease .
POMPE'S DISEASE .
0.68