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 .
C10.228.140.163.100.750 Pyruvate Dehydrogenase Complex Deficiency Disease .
C10.228.140.163.100.937 Urea Cycle Disorders, Inborn .
C10.228.140.163.100.937.500 Hyperargininemia .
C10.597 Neurologic Manifestations .
C10.597.606 Neurobehavioral Manifestations .
C10.597.606.643 Intellectual Disability .
C10.597.606.643.455 Mental Retardation, X-Linked .
C10.597.606.643.455.875 Pyruvate Dehydrogenase Complex Deficiency Disease .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.322 Genetic Diseases, X-Linked .
C16.320.322.500 Mental Retardation, X-Linked .
C16.320.322.500.875 Pyruvate Dehydrogenase Complex Deficiency Disease .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.525 Mental Retardation, X-Linked .
C16.320.400.525.875 Pyruvate Dehydrogenase Complex Deficiency Disease .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.100 Amino Acid Metabolism, Inborn Errors .
C16.320.565.100.940 Urea Cycle Disorders, Inborn .
C16.320.565.100.940.500 Hyperargininemia .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.750 Pyruvate Dehydrogenase Complex Deficiency Disease .
C16.320.565.189.937 Urea Cycle Disorders, Inborn .
C16.320.565.189.937.500 Hyperargininemia .
C16.320.565.202 Carbohydrate Metabolism, Inborn Errors .
C16.320.565.202.810 Pyruvate Metabolism, Inborn Errors .
C16.320.565.202.810.766 Pyruvate Dehydrogenase Complex Deficiency Disease .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.750 Pyruvate Dehydrogenase Complex Deficiency Disease .
C18.452.132.100.937 Urea Cycle Disorders, Inborn .
C18.452.132.100.937.437 Hyperargininemia .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.100 Amino Acid Metabolism, Inborn Errors .
C18.452.648.100.940 Urea Cycle Disorders, Inborn .
C18.452.648.100.940.437 Hyperargininemia .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.750 Pyruvate Dehydrogenase Complex Deficiency Disease .
C18.452.648.189.937 Urea Cycle Disorders, Inborn .
C18.452.648.189.937.437 Hyperargininemia .
C18.452.648.202 Carbohydrate Metabolism, Inborn Errors .
C18.452.648.202.810 Pyruvate Metabolism, Inborn Errors .
C18.452.648.202.810.766 Pyruvate Dehydrogenase Complex Deficiency Disease .
C18.452.660 Mitochondrial Diseases .
C18.452.660.710 Pyruvate Dehydrogenase Complex Deficiency Disease .
C18.654 Nutrition Disorders .
C18.654.521 Malnutrition .
C18.654.521.500 Deficiency Diseases .
SP6 Nutrition, Public Health .
SP6.016 Nutrition Disorders .
SP6.016.052 Deficiency Diseases .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
Deficiency Diseases .
Deficiency Disease .
Disease, Deficiency .
Diseases, Deficiency .
1.00
 
Hyperargininemia .
Deficiency Disease, Arginase .
ARG1 Deficiencies .
Arginase Deficiencies .
Arginase Deficiency Diseases .
Deficiencies, ARG1 .
Deficiencies, Arginase .
Deficiency Diseases, Arginase .
Deficiency, ARG1 .
Deficiency, Arginase .
Hyperargininemias .
Arginase Deficiency Disease .
Argininemia .
ARG1 Deficiency .
Arginase Deficiency .
0.81
 
/deficiency .
0.79
 
Pyruvate Dehydrogenase Complex Deficiency Disease .
Ataxia with Lactic Acidosis .
Ataxia with Lactic Acidosis I .
Ataxia, Intermittent, with Abnormal Pyruvate Metabolism .
Ataxia, Intermittent, with Pyruvate Dehydrogenase, or Decarboxylase, Deficiency .
Intermittent Ataxia with Pyruvate Dehydrogenase Deficiency .
Juvenile Pyruvate Dehydrogenase Complex Deficiency Disease .
Neonatal Pyruvate Dehydrogenase Complex Deficiency Disease .
PDH Deficiency .
PDHC Deficiency .
PDHC Deficiency Disease .
Pyruvate Decarboxylase Deficiency .
Pyruvate Dehydrogenase Complex Deficiency .
Pyruvate Dehydrogenase Complex Deficiency Disease, Juvenile .
Pyruvate Dehydrogenase Complex Deficiency Disease, Neonatal .
Pyruvate Dehydrogenase Deficiency .
Type I Ataxia with Lactic Acidosis .
Deficiency, PDH .
Deficiency, PDHC .
Deficiency, Pyruvate Decarboxylase .
Deficiency, Pyruvate Dehydrogenase .
Ataxia with Lactic Acidosis, Type I .
Lactic Acidosis with Ataxia, Type I .
PYRUVATE DEHYDROGENASE COMPLEX DEFICIENCY .
0.78