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 .
C10.228.140.163.100.593 Mevalonate Kinase Deficiency .
C10.228.140.163.100.937 Urea Cycle Disorders, Inborn .
C10.228.140.163.100.937.374 Citrullinemia .
C10.228.140.163.100.937.500 Hyperargininemia .
C10.597 Neurologic Manifestations .
C10.597.606 Neurobehavioral Manifestations .
C10.597.606.643 Intellectual Disability .
C15 Hemic and Lymphatic Diseases .
C15.378 Hematologic Diseases .
C15.378.147 Blood Protein Disorders .
C15.378.147.542 Hypergammaglobulinemia .
C15.378.147.542.319 Mevalonate Kinase Deficiency .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.382 Hereditary Autoinflammatory Diseases .
C16.320.382.750 Mevalonate Kinase Deficiency .
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 .
C16.320.565.100.940.500 Hyperargininemia .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.593 Mevalonate Kinase Deficiency .
C16.320.565.189.937 Urea Cycle Disorders, Inborn .
C16.320.565.189.937.374 Citrullinemia .
C16.320.565.189.937.500 Hyperargininemia .
C16.320.565.663 Peroxisomal Disorders .
C16.320.565.663.430 Mevalonate Kinase Deficiency .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.593 Mevalonate Kinase Deficiency .
C18.452.132.100.937 Urea Cycle Disorders, Inborn .
C18.452.132.100.937.374 Citrullinemia .
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 .
C18.452.648.100.940.374 Citrullinemia .
C18.452.648.100.940.437 Hyperargininemia .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.593 Mevalonate Kinase Deficiency .
C18.452.648.189.937 Urea Cycle Disorders, Inborn .
C18.452.648.189.937.374 Citrullinemia .
C18.452.648.189.937.437 Hyperargininemia .
C18.452.648.663 Peroxisomal Disorders .
C18.452.648.663.430 Mevalonate Kinase Deficiency .
C20 Immune System Diseases .
C20.683 Immunoproliferative Disorders .
C20.683.460 Hypergammaglobulinemia .
C20.683.460.319 Mevalonate Kinase Deficiency .
C23 Pathological Conditions, Signs and Symptoms .
C23.888 Signs and Symptoms .
C23.888.592 Neurologic Manifestations .
C23.888.592.604 Neurobehavioral Manifestations .
C23.888.592.604.646 Intellectual Disability .
D02 Organic Chemicals .
D02.241 Carboxylic Acids .
D02.241.511 Hydroxy Acids .
D02.241.511.579 Mevalonic Acid .
F01 Behavior and Behavior Mechanisms .
F01.700 Neurobehavioral Manifestations .
F01.700.687 Intellectual Disability .
F03 Mental Disorders .
F03.625 Neurodevelopmental Disorders .
F03.625.539 Intellectual Disability .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
Mevalonate Kinase Deficiency .
Hyper IgD Syndrome .
Hyper-IgD Syndrome .
Hyperimmunoglobulinemia D And Periodic Fever Syndrome .
Mevalonic Aciduria .
Periodic Fever, Dutch Type .
Aciduria, Mevalonic .
Hyper IgD Syndromes .
Hyper-IgD Syndromes .
Kinase Deficiencies, Mevalonate .
Kinase Deficiency, Mevalonate .
Mevalonate Kinase Deficiencies .
Mevalonicacidurias .
Syndrome, Hyper-IgD .
Hyperimmunoglobulinemia D .
Mevalonicaciduria .
1.00
0164
 
Mevalonic Acid .
Mevalonate .
Acid, Mevalonic .
0.63
13194
 
Intellectual Disability .
Deficiency, Mental .
Intellectual Development Disorder .
Mental Deficiency .
Mental Retardation, Psychosocial .
Deficiencies, Mental .
Development Disorder, Intellectual .
Development Disorders, Intellectual .
Disabilities, Intellectual .
Disorder, Intellectual Development .
Disorders, Intellectual Development .
Intellectual Development Disorders .
Intellectual Disabilities .
Mental Deficiencies .
Mental Retardations, Psychosocial .
Psychosocial Mental Retardation .
Psychosocial Mental Retardations .
Retardation, Psychosocial Mental .
Retardations, Psychosocial Mental .
Disability, Intellectual .
Idiocy .
Mental Retardation .
Retardation, Mental .
MENTAL DEFICIENCY .
MENTAL RETARDATION, PSYCHOSOCIAL .
0.53
 
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 .
0.51
0174
 
/deficiency .
0.51
 
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 .
0.51
6245