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 .
C10.228.140.163.100.937 Urea Cycle Disorders, Inborn .
C10.228.140.163.100.937.374 Citrullinemia .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.100 Amino Acid Metabolism, Inborn Errors .
C16.320.565.100.940 Urea Cycle Disorders, Inborn .
C16.320.565.100.940.374 Citrullinemia .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.937 Urea Cycle Disorders, Inborn .
C16.320.565.189.937.374 Citrullinemia .
C16.320.565.202 Carbohydrate Metabolism, Inborn Errors .
C16.320.565.202.251 Fructose Metabolism, Inborn Errors .
C16.320.565.202.251.271 Fructose Intolerance .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.937 Urea Cycle Disorders, Inborn .
C18.452.132.100.937.374 Citrullinemia .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.100 Amino Acid Metabolism, Inborn Errors .
C18.452.648.100.940 Urea Cycle Disorders, Inborn .
C18.452.648.100.940.374 Citrullinemia .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.937 Urea Cycle Disorders, Inborn .
C18.452.648.189.937.374 Citrullinemia .
C18.452.648.202 Carbohydrate Metabolism, Inborn Errors .
C18.452.648.202.251 Fructose Metabolism, Inborn Errors .
C18.452.648.202.251.271 Fructose Intolerance .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
Fructose Intolerance .
ALDOB Deficiency .
Aldolase B Deficiency .
Fructose Aldolase B Deficiency .
Fructose Intolerance, Hereditary .
Fructose-1,6-Biphosphate Aldolase Deficiency .
Fructose-1,6-Bisphosphate Aldolase B Deficiency .
Fructose-1-Phosphate Aldolase Deficiency .
Fructosemia .
Hereditary Fructose Intolerance .
ALDOB Deficiencies .
Aldolase B Deficiencies .
Aldolase Deficiencies, Fructose-1,6-Biphosphate .
Aldolase Deficiencies, Fructose-1-Phosphate .
Aldolase Deficiency, Fructose-1,6-Biphosphate .
Aldolase Deficiency, Fructose-1-Phosphate .
Deficiencies, ALDOB .
Deficiencies, Aldolase B .
Deficiencies, Fructose-1,6-Biphosphate Aldolase .
Deficiencies, Fructose-1-Phosphate Aldolase .
Deficiency, ALDOB .
Deficiency, Aldolase B .
Deficiency, Fructose-1,6-Biphosphate Aldolase .
Deficiency, Fructose-1-Phosphate Aldolase .
Fructose 1 Phosphate Aldolase Deficiency .
Fructose 1,6 Biphosphate Aldolase Deficiency .
Fructose 1,6 Bisphosphate Aldolase B Deficiency .
Fructose Intolerances .
Fructose Intolerances, Hereditary .
Fructose-1,6-Biphosphate Aldolase Deficiencies .
Fructose-1-Phosphate Aldolase Deficiencies .
Fructosemias .
Hereditary Fructose Intolerances .
Intolerance, Fructose .
Intolerances, Fructose .
1.00
 
/deficiency .
0.72
 
Citrullinemia .
Argininosuccinic Acid Synthase Deficiency Disease .
Argininosuccinic Acid Synthetase Deficiency Disease .
Argininosuccinic Acid Synthetase Deficiency Disease, Partial .
Argininosuccinic Acid Synthetase Deficiency, Complete .
Citrullinemia, Classical .
Citrullinemia, Late-Onset .
Citrullinemia, Neonatal .
Citrullinemia, Type I .
Citrullinuria .
Complete Argininosuccinic Acid Synthetase Deficiency Disease .
Deficiency, Argininosuccinic Acid Synthetase, Complete .
Deficiency, Argininosuccinic Acid Synthetase, Partial .
Partial Argininosuccinic Acid Synthetase Deficiency Disease .
ASS Deficiencies .
Argininosuccinate Synthetase Deficiencies .
Citrullinemia, Late Onset .
Citrullinemias .
Citrullinemias, Classic .
Citrullinemias, Classical .
Citrullinemias, Late-Onset .
Citrullinemias, Neonatal .
Citrullinurias .
Classic Citrullinemia .
Classic Citrullinemias .
Classical Citrullinemia .
Classical Citrullinemias .
Deficiencies, ASS .
Deficiencies, Argininosuccinate Synthetase .
Deficiency, ASS .
Deficiency, Argininosuccinate Synthetase .
Late-Onset Citrullinemia .
Late-Onset Citrullinemias .
Neonatal Citrullinemia .
Neonatal Citrullinemias .
Type 1, Citrullinemia .
Argininosuccinate Synthase Deficiency Disease .
Argininosuccinate Synthetase Deficiency .
Argininosuccinic Acid Synthetase Deficiency .
ASS Deficiency .
Citrullinemia 1 .
Citrullinemia Type 1 .
Citrullinemia, Classic .
Deficiency Disease, Argininosuccinate Synthase .
Deficiency Disease, Argininosuccinic Acid Synthase .
0.68