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 .
C10.597 Neurologic Manifestations .
C10.597.606 Neurobehavioral Manifestations .
C10.597.606.643 Intellectual Disability .
C10.597.606.643.455 Mental Retardation, X-Linked .
C10.597.606.643.455.562 Glycogen Storage Disease Type IIb .
C14 Cardiovascular Diseases .
C14.280 Heart Diseases .
C14.280.238 Cardiomyopathies .
C14.280.238.458 Glycogen Storage Disease Type IIb .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.322 Genetic Diseases, X-Linked .
C16.320.322.201 Glycogen Storage Disease Type IIb .
C16.320.322.217 Glycogen Storage Disease Type VIII .
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 .
C16.320.565.202.449.448 Glycogen Storage Disease Type I .
C16.320.565.202.449.500 Glycogen Storage Disease Type II .
C16.320.565.202.449.510 Glycogen Storage Disease Type IIb .
C16.320.565.202.449.520 Glycogen Storage Disease Type III .
C16.320.565.202.449.540 Glycogen Storage Disease Type IV .
C16.320.565.202.449.560 Glycogen Storage Disease Type V .
C16.320.565.202.449.620 Glycogen Storage Disease Type VIII .
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 .
C18.452.648.202.449.448 Glycogen Storage Disease Type I .
C18.452.648.202.449.500 Glycogen Storage Disease Type II .
C18.452.648.202.449.510 Glycogen Storage Disease Type IIb .
C18.452.648.202.449.520 Glycogen Storage Disease Type III .
C18.452.648.202.449.540 Glycogen Storage Disease Type IV .
C18.452.648.202.449.560 Glycogen Storage Disease Type V .
C18.452.648.202.449.620 Glycogen Storage Disease Type VIII .
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 I .
Deficiency, Glucosephosphatase .
Gierke Disease .
Gierke's Disease .
Glycogen Storage Disease 1 (GSD I) .
von Gierke's Disease .
Deficiencies, Glucose-6-Phosphatase .
Deficiencies, Glucosephosphatase .
Deficiency, Glucose-6-Phosphatase .
Disease, Gierke .
Disease, Gierke's .
Disease, von Gierke .
Disease, von Gierke's .
Gierkes Disease .
Glucose 6 Phosphatase Deficiency .
Glucose-6-Phosphatase Deficiencies .
Glucosephosphatase Deficiencies .
von Gierkes Disease .
Glucosephosphatase Deficiency .
Glucose-6-Phosphatase Deficiency .
Glycogenosis 1 .
Hepatorenal Glycogen Storage Disease .
von Gierke Disease .
Von Gierke's Disease .
0.88
 
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 .
0.88
 
Glycogen Storage Disease Type IV .
Andersen's Disease .
Deficiency, Brancher .
Gbe1 Deficiency .
Glycogen Branching Enzyme Deficiency .
Glycogen Storage Disease Type 4 .
Glycogenosis IV .
Type IV Glycogenosis .
Amylopectinoses .
Andersens Disease .
Brancher Deficiencies .
Deficiencies, Brancher .
Deficiencies, Gbe1 .
Deficiency, Gbe1 .
Disease, Andersen .
Disease, Andersen's .
Gbe1 Deficiencies .
Glycogenoses, Type IV .
Glycogenosis 4s .
Glycogenosis IVs .
Glycogenosis, Type IV .
Type IV Glycogenoses .
Amylopectinosis .
Andersen Disease .
Brancher Deficiency .
Glycogenosis 4 .
0.87
 
Glycogen Storage Disease Type IIb .
Antopol Disease .
Danon Disease .
Glycogen Storage Cardiomyopathy .
Glycogen Storage Disease IIb .
Glycogen Storage Disease Limited to the Heart .
Glycogen Storage Disease Type 2B .
Lysosomal Glycogen Storage Disease with Normal Acid Maltase .
Lysosomal Glycogen Storage Disease without Acid Maltase Deficiency .
Pseudoglycogenosis 2 .
Pseudoglycogenosis II .
Vacuolar Cardiomyopathy and Myopathy, X-linked .
X-Linked Vacuolar Cardiomyopathy and Myopathy .
Cardiomyopathies, Glycogen Storage .
Cardiomyopathy, Glycogen Storage .
Disease, Antopol .
Glycogen Storage Cardiomyopathies .
Pseudoglycogenosis 2s .
Pseudoglycogenosis IIs .
Vacuolar Cardiomyopathy and Myopathy, X linked .
X Linked Vacuolar Cardiomyopathy and Myopathy .
0.86
 
Glycogen Storage Disease Type VIII .
Glycogenosis 8 .
0.84
 
Glycogen Storage Disease Type V .
Deficiency, Muscle Phosphorylase .
Glycogen Storage Disease Type 5 .
Glycogen Storage Disease V .
McArdle Disease .
McArdle Type Glycogen Storage Disease .
Mcardle Syndrome .
Muscle Glycogen Phosphorylase Deficiency .
Muscle Phosphorylase Deficiency .
Myophosphorylase deficiency .
PYGM Deficiency .
Deficiencies, Muscle Phosphorylase .
Deficiencies, PYGM .
Deficiency, PYGM .
Disease, McArdle .
Disease, McArdle's .
Glycogenosis 5s .
McArdles Disease .
Mcardle Syndromes .
Muscle Phosphorylase Deficiencies .
Myophosphorylase deficiencies .
PYGM Deficiencies .
Phosphorylase Deficiencies, Muscle .
Phosphorylase Deficiency, Muscle .
Syndrome, Mcardle .
Syndromes, Mcardle .
deficiencies, Myophosphorylase .
deficiency, Myophosphorylase .
Glycogenosis 5 .
McArdle's Disease .
0.83