serw-MX  [xml]  
 


    
 Categorias DeCS

C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.595 Lysosomal Storage Diseases .
C16.320.565.595.100 Aspartylglucosaminuria .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.595 Lysosomal Storage Diseases .
C18.452.648.595.100 Aspartylglucosaminuria .
D08 Enzymes and Coenzymes .
D08.811 Enzymes .
D08.811.277 Hydrolases .
D08.811.277.087 Amidohydrolases .
D08.811.277.087.125 Aspartylglucosylaminase .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
Aspartylglucosaminuria .
AGA Deficiency .
Aspartylglucosamidase Deficiency .
Aspartylglycosaminuria .
Glycoasparaginase .
AGA Deficiencies .
Aspartylglucosamidase Deficiencies .
Aspartylglucosaminurias .
Aspartylglycosaminurias .
Deficiencies, AGA .
Deficiencies, Aspartylglucosamidase .
Deficiency, AGA .
Deficiency, Aspartylglucosamidase .
Glycoasparaginases .
1.00
 
Aspartylglucosylaminase .
Aspartylglucosamine Amidohydrolase .
Glycosylasparaginase .
Amidohydrolase, Aspartylglucosamine .
Amidohydrolase, Aspartylglycosamine .
Deaspartylase, Aspartylglucosylamine .
Aspartylglucosaminidase .
Aspartylglucosylamine Deaspartylase .
Aspartylglycosamine Amidohydrolase .
0.81