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 .
C16.131 Congenital Abnormalities .
C16.131.077 Abnormalities, Multiple .
C16.131.077.735 Prolidase Deficiency .
C16.131.831 Skin Abnormalities .
C16.131.831.720 Prolidase Deficiency .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.100 Amino Acid Metabolism, Inborn Errors .
C16.320.565.100.794 Prolidase Deficiency .
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 .
C16.320.565.202.449 Glycogen Storage Disease .
C16.320.565.202.449.560 Glycogen Storage Disease Type V .
C16.320.850 Skin Diseases, Genetic .
C16.320.850.746 Prolidase Deficiency .
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 .
C18.452.648.202.449 Glycogen Storage Disease .
C18.452.648.202.449.560 Glycogen Storage Disease Type V .
C18.654 Nutrition Disorders .
C18.654.521 Malnutrition .
C18.654.521.500 Deficiency Diseases .
C18.654.521.500.708 Protein Deficiency .
SP6 Nutrition, Public Health .
SP6.016 Nutrition Disorders .
SP6.016.052 Deficiency Diseases .
SP6.016.052.058 Malnutrition .
SP6.016.052.058.089 Protein Deficiency .
 
 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
 
Protein Deficiency .
Deficiency, Protein .
Deficiencies, Protein .
Protein Deficiencies .
Protein Malnutrition .
0.68
 
/deficiency .
0.65
 
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 .
0.64
 
Prolidase Deficiency .
Hyperimidodipeptiduria .
Imidodipeptidase Deficiency .
Deficiencies, Imidodipeptidase .
Deficiencies, Prolidase .
Deficiency, Imidodipeptidase .
Deficiency, Prolidase .
Hyperimidodipeptidurias .
Imidodipeptidase Deficiencies .
Prolidase Deficiencies .
0.63