Categorias DeCS
A08 Nervous System .
A08.800 Peripheral Nervous System .
A08.800.050 Autonomic Nervous System .
A08.800.050.050 Autonomic Pathways .
A08.800.050.050.275 Facial Nerve .
A08.800.050.600 Parasympathetic Nervous System .
A08.800.050.600.149 Facial Nerve .
A08.800.800 Peripheral Nerves .
A08.800.800.060 Autonomic Pathways .
A08.800.800.060.275 Facial Nerve .
A08.800.800.120 Cranial Nerves .
A08.800.800.120.250 Facial Nerve .
C05 Musculoskeletal Diseases .
C05.651 Muscular Diseases .
C05.651.534 Muscular Disorders, Atrophic .
C05.651.534.500 Muscular Dystrophies .
C05.651.534.500.149 Glycogen Storage Disease Type VII .
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 .
C10.668 Neuromuscular Diseases .
C10.668.491 Muscular Diseases .
C10.668.491.175 Muscular Disorders, Atrophic .
C10.668.491.175.500 Muscular Dystrophies .
C10.668.491.175.500.112 Glycogen Storage Disease Type VII .
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 .
C16.320.565.202.449.600 Glycogen Storage Disease Type VII .
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 .
C16.320.577 Muscular Dystrophies .
C16.320.577.149 Glycogen Storage Disease Type VII .
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 .
C18.452.648.202.449.600 Glycogen Storage Disease Type VII .
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 .
D03 Heterocyclic Compounds .
D03.383 Heterocyclic Compounds, 1-Ring .
D03.383.606 Piperazines .
D03.383.606.980 Vilazodone Hydrochloride .
D03.633 Heterocyclic Compounds, Fused-Ring .
D03.633.100 Heterocyclic Compounds, 2-Ring .
D03.633.100.127 Benzofurans .
D03.633.100.127.818 Vilazodone Hydrochloride .
D03.633.100.473 Indoles .
D03.633.100.473.957 Vilazodone Hydrochloride .
D08 Enzymes and Coenzymes .
D08.622 Enzyme Precursors .
D08.622.432 Factor VII .
D08.811 Enzymes .
D08.811.277 Hydrolases .
D08.811.277.656 Peptide Hydrolases .
D08.811.277.656.300 Endopeptidases .
D08.811.277.656.300.760 Serine Endopeptidases .
D08.811.277.656.300.760.300 Factor VIIa .
D08.811.277.656.300.760.787 Subtilisins .
D08.811.277.656.959 Serine Proteases .
D08.811.277.656.959.350 Serine Endopeptidases .
D08.811.277.656.959.350.300 Factor VIIa .
D08.811.277.656.959.350.787 Subtilisins .
D12 Amino Acids, Peptides, and Proteins .
D12.776 Proteins .
D12.776.124 Blood Proteins .
D12.776.124.125 Blood Coagulation Factors .
D12.776.124.125.325 Factor VII .
D12.776.124.125.325.300 Factor VIIa .
D12.776.124.125.350 Factor VIII .
D23 Biological Factors .
D23.119 Blood Coagulation Factors .
D23.119.325 Factor VII .
D23.119.325.300 Factor VIIa .
D23.119.350 Factor VIII .
Termos Sinônimos e Históricos Documentos LILACS e MDL
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 . 0.58