serw-MX  [xml]  

 DeCS Categories

C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.163 Brain Diseases, Metabolic .
C10. Brain Diseases, Metabolic, Inborn .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.202 Carbohydrate Metabolism, Inborn Errors .
C16.320.565.398 Lipid Metabolism, Inborn Errors .
C16.320.565.618 Metal Metabolism, Inborn Errors .
C16.320.565.798 Purine-Pyrimidine Metabolism, Inborn Errors .
C16.320.565.925 Steroid Metabolism, Inborn Errors .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.584 Lipid Metabolism Disorders .
C18.452.584.562 Lipid Metabolism, Inborn Errors .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.202 Carbohydrate Metabolism, Inborn Errors .
C18.452.648.398 Lipid Metabolism, Inborn Errors .
C18.452.648.618 Metal Metabolism, Inborn Errors .
C18.452.648.798 Purine-Pyrimidine Metabolism, Inborn Errors .
C18.452.648.925 Steroid Metabolism, Inborn Errors .
 Synonyms & Historicals
Metal Metabolism, Inborn Errors .
Metal Metabolism, Inborn Error .
Dysfunctions in the metabolism of metals resulting from inborn genetic mutations that are inherited or acquired in utero. .
Carbohydrate Metabolism, Inborn Errors .
Carbohydrate Metabolism, Inborn Error .
Dysfunctions of CARBOHYDRATE METABOLISM resulting from inborn genetic mutations that are inherited or acquired in utero. .
Purine-Pyrimidine Metabolism, Inborn Errors .
Purine Pyrimidine Metabolism, Inborn Errors .
Dysfunctions in the metabolism of PURINES or PYRIMIDINES resulting from inborn genetic mutations that are inherited or acquired in utero. .
Metabolism, Inborn Errors .
Metabolism Errors, Inborn .
Error, Inborn Metabolism .
Errors Metabolism, Inborn .
Errors Metabolisms, Inborn .
Errors, Inborn Metabolism .
Inborn Errors Metabolism .
Inborn Errors Metabolisms .
Inborn Metabolism Error .
Inborn Metabolism Errors .
Metabolism Error, Inborn .
Metabolism Inborn Error .
Metabolism Inborn Errors .
Metabolisms, Inborn Errors .
Inborn Errors of Metabolism .
Errors in metabolic processes resulting from inborn genetic mutations that are inherited or acquired in utero. .
Steroid Metabolism, Inborn Errors .
Congenital Errors of Steroid Metabolism .
Inborn Errors of Steroid Metabolism .
Steroid Metabolic Diseases, Inborn .
Errors in metabolic processing of STEROIDS resulting from inborn genetic mutations that are inherited or acquired in utero. .
Lipid Metabolism, Inborn Errors .
Lipid Metabolism, Inborn Error .
Errors in the metabolism of LIPIDS resulting from inborn genetic MUTATIONS that are heritable. .
Brain Diseases, Metabolic, Inborn .
Brain Diseases, Metabolic, Familial .
Brain Diseases, Metabolic, Inherited .
Brain Syndrome, Metabolic, Inborn .
CNS Metabolic Disorders, Inborn .
Central Nervous System Inborn Metabolic Disorders .
Encephalopathies, Metabolic, Inborn .
Familial Metabolic Disorders, Brain .
Inborn Metabolic Brain Diseases .
Inborn Metabolic Brain Disorders .
Inborn Metabolic Disorders, Brain .
Inherited Metabolic Brain Diseases .
Inherited Metabolic Disorders, Brain .
Metabolic Brain Diseases, Familial .
Metabolic Brain Diseases, Inborn .
Metabolic Brain Diseases, Inherited .
Metabolic Brain Syndrome, Inborn .
Metabolic Diseases, Inborn, Central Nervous System .
Metabolic Disorders, Brain, Inherited .
Metabolic Disorders, CNS, Inborn .
Metabolic Disorders, Familial, Brain .
Central Nervous System Inborn Metabolic Diseases .
Familial Metabolic Brain Diseases .
Inborn Errors of Metabolism, Brain .
Metabolic Diseases, Inborn, Brain .
Brain disorders resulting from inborn metabolic errors, primarily from enzymatic defects which lead to substrate accumulation, product reduction, or increase in toxic metabolites through alternate pathways. The majority of these conditions are familial, however spontaneous mutation may also occur in utero. .