serw-MX  [xml]  
 


    
 Categorias DeCS

C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.202 Carbohydrate Metabolism, Inborn Errors .
C16.320.565.202.449 Glycogen Storage Disease .
C16.320.565.202.449.560 Glycogen Storage Disease Type V .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.202 Carbohydrate Metabolism, Inborn Errors .
C18.452.648.202.449 Glycogen Storage Disease .
C18.452.648.202.449.560 Glycogen Storage Disease Type V .
D08 Enzymes and Coenzymes .
D08.811 Enzymes .
D08.811.913 Transferases .
D08.811.913.400 Glycosyltransferases .
D08.811.913.400.450 Hexosyltransferases .
D08.811.913.400.450.460 Glucosyltransferases .
D08.811.913.400.450.460.400 Phosphorylases .
D08.811.913.400.450.460.400.186 Glycogen Phosphorylase .
D08.811.913.400.450.460.400.186.312 Glycogen Phosphorylase, Muscle Form .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
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 .
1.00
 
Glycogen Phosphorylase, Muscle Form .
Glycogen Phosphorylase a, Muscle Form .
Glycogen Phosphorylase b, Muscle Form .
Myophosphorylase a and b .
Myophosphorylase .
0.73