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 Categorias DeCS

C06 Digestive System Diseases .
C06.689 Pancreatic Diseases .
C06.689.150 Congenital Hyperinsulinism .
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 .
C10.228.140.163.100.380 Hyperlysinemias .
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 .
C16.320.565.100.544 Hyperlysinemias .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.380 Hyperlysinemias .
C16.614 Infant, Newborn, Diseases .
C16.614.200 Congenital Hyperinsulinism .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.380 Hyperlysinemias .
C18.452.394 Glucose Metabolism Disorders .
C18.452.394.968 Hyperinsulinism .
C18.452.394.968.250 Congenital Hyperinsulinism .
C18.452.394.984 Hypoglycemia .
C18.452.394.984.200 Congenital Hyperinsulinism .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.100 Amino Acid Metabolism, Inborn Errors .
C18.452.648.100.544 Hyperlysinemias .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.380 Hyperlysinemias .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
Congenital Hyperinsulinism .
Familial Hyperinsulinemic Hypoglycemia 1 .
Familial Hyperinsulinism .
Hyperinsulinemia Hypoglycemia of Infancy .
Hyperinsulinemic Hypoglycemia Due to Focal Adenomatous Hyperplasia .
Hyperinsulinemic Hypoglycemia, Familial, 1 .
Hyperinsulinemic Hypoglycemia, Familial, 2 .
Hyperinsulinemic Hypoglycemia, Persistent .
Hyperinsulinism, Congenital .
Hyperinsulinism, Familial .
Hyperinsulinism, Neonatal .
Hypoglycemia, Hyperinsulinemic, of Infancy .
Infancy Hyperinsulinemia Hypoglycemia .
Neonatal Hyperinsulinism .
PHHI Hypoglycemia .
Persistent Hyperinsulinemic Hypoglycemia .
Congenital Hyperinsulinisms .
Familial Hyperinsulinisms .
Hyperinsulinemic Hypoglycemias, Persistent .
Hyperinsulinisms, Congenital .
Hyperinsulinisms, Familial .
Hyperinsulinisms, Neonatal .
Hypoglycemia, PHHI .
Hypoglycemia, Persistent Hyperinsulinemic .
Hypoglycemias, PHHI .
Hypoglycemias, Persistent Hyperinsulinemic .
Infancy Hyperinsulinemia Hypoglycemias .
Neonatal Hyperinsulinisms .
PHHI Hypoglycemias .
Persistent Hyperinsulinemic Hypoglycemias .
Persistent Hyperinsulinemia Hypoglycemia of Infancy .
1.00
 
Hyperinsulinism .
Compensatory Hyperinsulinemia .
Endogenous Hyperinsulinism .
Exogenous Hyperinsulinism .
Hyperinsulinemia .
Hyperinsulinemia, Compensatory .
Hyperinsulinism, Endogenous .
Hyperinsulinism, Exogenous .
Hyperinsulinemia .
0.75
 
Hyperlysinemias .
Deficiency Disease, Alpha-Aminoadipic Semialdehyde .
Deficiency Disease, Lysine Alpha-Ketoglutarate Reductase .
Deficiency Disease, Saccharopine Dehydrogenase .
Familial Hyperlysinemia .
Hyperlysinemia .
Hyperlysinemia, Familial .
Hyperlysinemia, Periodic .
Hyperlysinuria With Hyperammonemia .
L-Lysine:NAD-Oxido-Reductase Deficiency .
Lysine:Alpha-Ketoglutarate Reductase Deficiency .
Alpha Aminoadipic Semialdehyde Deficiency Disease .
Deficiencies, L-Lysine:NAD-Oxido-Reductase .
Deficiencies, Lysine:Alpha-Ketoglutarate Reductase .
Deficiency Disease, Alpha Aminoadipic Semialdehyde .
Deficiency Disease, Lysine Alpha Ketoglutarate Reductase .
Deficiency, L-Lysine:NAD-Oxido-Reductase .
Deficiency, Lysine:Alpha-Ketoglutarate Reductase .
Familial Hyperlysinemias .
Hyperammonemia, Hyperlysinuria With .
Hyperammonemias, Hyperlysinuria With .
Hyperlysinemias, Familial .
Hyperlysinemias, Periodic .
Hyperlysinuria With Hyperammonemias .
L Lysine:NAD Oxido Reductase Deficiency .
L-Lysine:NAD-Oxido-Reductase Deficiencies .
Lysine Alpha Ketoglutarate Reductase Deficiency Disease .
Lysine:Alpha Ketoglutarate Reductase Deficiency .
Lysine:Alpha-Ketoglutarate Reductase Deficiencies .
Periodic Hyperlysinemia .
Periodic Hyperlysinemias .
Reductase Deficiencies, Lysine:Alpha-Ketoglutarate .
Reductase Deficiency, Lysine:Alpha-Ketoglutarate .
With Hyperammonemia, Hyperlysinuria .
With Hyperammonemias, Hyperlysinuria .
Alpha-Aminoadipic Semialdehyde Deficiency Disease .
Lysine Alpha-Ketoglutarate Reductase Deficiency Disease .
Saccharopine Dehydrogenase Deficiency Disease .
0.61