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 .
C10.228.140.163.100.937.750 Ornithine Carbamoyltransferase Deficiency Disease .
C11 Eye Diseases .
C11.270 Eye Diseases, Hereditary .
C11.270.468 Gyrate Atrophy .
C11.941 Uveal Diseases .
C11.941.160 Choroid Diseases .
C11.941.160.578 Gyrate Atrophy .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.290 Eye Diseases, Hereditary .
C16.320.290.468 Gyrate Atrophy .
C16.320.322 Genetic Diseases, X-Linked .
C16.320.322.828 Ornithine Carbamoyltransferase 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 .
C16.320.565.100.940.374 Citrullinemia .
C16.320.565.100.940.750 Ornithine Carbamoyltransferase Deficiency Disease .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.937 Urea Cycle Disorders, Inborn .
C16.320.565.189.937.374 Citrullinemia .
C16.320.565.189.937.750 Ornithine Carbamoyltransferase 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 .
C18.452.132.100.937 Urea Cycle Disorders, Inborn .
C18.452.132.100.937.374 Citrullinemia .
C18.452.132.100.937.500 Ornithine Carbamoyltransferase Deficiency Disease .
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 .
C18.452.648.100.940.500 Ornithine Carbamoyltransferase Deficiency Disease .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.937 Urea Cycle Disorders, Inborn .
C18.452.648.189.937.374 Citrullinemia .
C18.452.648.189.937.500 Ornithine Carbamoyltransferase Deficiency Disease .
C23 Pathological Conditions, Signs and Symptoms .
C23.888 Signs and Symptoms .
C23.888.852 Signs and Symptoms, Respiratory .
C23.888.852.079 Hypoxia .
D01 Inorganic Chemicals .
D01.268 Elements .
D01.268.185 Chalcogens .
D01.268.185.550 Oxygen .
D01.362 Gases .
D01.362.670 Oxygen .
SP4 Environmental Health .
SP4.011 Science .
SP4.011.097 Chemistry .
SP4.011.097.063 Elements .
SP4.011.097.063.949 Oxygen .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
Hypoxia .
Anoxemia .
Deficiency, Oxygen .
Hypoxemia .
Deficiencies, Oxygen .
Oxygen Deficiencies .
Anoxia .
Oxygen Deficiency .
1.00
72254952
 
/deficiency .
0.72
 
Oxygen .
Oxygen-16 .
Oxygen 16 .
Dioxygen .
0.64
611145639
 
Gyrate Atrophy .
Gyrate Atrophy of Choroid and Retina .
Gyrate Atrophy of the Choroid and Retina .
Hyperornithinemia with Gyrate Atrophy of Choroid and Retina .
OAT Deficiency .
OKT Deficiency .
Ornithine Aminotransferase Deficiency .
Ornithine Keto Acid Aminotransferase Deficiency .
Ornithine Ketoacid Aminotransferase Deficiency .
Ornithine-Delta-Aminotransferase Deficiency .
Ornithinemia with Gyrate Atrophy .
Atrophy, Gyrate .
Deficiency, OAT .
Deficiency, OKT .
Deficiency, Ornithine Aminotransferase .
Deficiency, Ornithine-Delta-Aminotransferase .
Ornithine Delta Aminotransferase Deficiency .
0.64
5124
 
Ornithine Carbamoyltransferase Deficiency Disease .
Deficiency Disease, Ornithine Carbamoyltransferase .
Deficiency Disease, Ornithine Transcarbamylase .
Ornithine Carbamoyltransferase Deficiency .
Ornithine Transcarbamylase Deficiency, Hyperammonemia Due To .
Deficiencies, OTC .
Deficiencies, Ornithine Transcarbamylase .
Deficiency, OTC .
Deficiency, Ornithine Transcarbamylase .
OTC Deficiencies .
Ornithine Transcarbamylase Deficiencies .
Ornithine Transcarbamylase Deficiency Disease .
Ornithine Transcarbamylase Deficiency .
OTC Deficiency .
0.62
3866
 
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 .
0.60
6245