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 Categorias DeCS

C10 Nervous System Diseases .
C10.177 Autonomic Nervous System Diseases .
C10.177.195 Complex Regional Pain Syndromes .
C10.177.195.200 Causalgia .
C10.177.195.800 Reflex Sympathetic Dystrophy .
C10.668 Neuromuscular Diseases .
C10.668.829 Peripheral Nervous System Diseases .
C10.668.829.250 Complex Regional Pain Syndromes .
C10.668.829.250.200 Causalgia .
C10.668.829.250.800 Reflex Sympathetic Dystrophy .
C10.668.829.600 Neuralgia .
C10.668.829.600.200 Causalgia .
C12 Male Urogenital Diseases .
C12.777 Urologic Diseases .
C12.777.419 Kidney Diseases .
C12.777.419.815 Renal Tubular Transport, Inborn Errors .
C12.777.419.815.770 Pseudohypoaldosteronism .
C13 Female Urogenital Diseases and Pregnancy Complications .
C13.351 Female Urogenital Diseases .
C13.351.968 Urologic Diseases .
C13.351.968.419 Kidney Diseases .
C13.351.968.419.815 Renal Tubular Transport, Inborn Errors .
C13.351.968.419.815.770 Pseudohypoaldosteronism .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.202 Carbohydrate Metabolism, Inborn Errors .
C16.320.565.202.715 Mucopolysaccharidoses .
C16.320.565.202.715.640 Mucopolysaccharidosis I .
C16.320.565.398 Lipid Metabolism, Inborn Errors .
C16.320.565.398.465 Hyperlipoproteinemia Type I .
C16.320.565.595 Lysosomal Storage Diseases .
C16.320.565.595.600 Mucopolysaccharidoses .
C16.320.565.595.600.640 Mucopolysaccharidosis I .
C16.320.565.861 Renal Tubular Transport, Inborn Errors .
C16.320.565.861.770 Pseudohypoaldosteronism .
C17 Skin and Connective Tissue Diseases .
C17.300 Connective Tissue Diseases .
C17.300.550 Mucinoses .
C17.300.550.575 Mucopolysaccharidoses .
C17.300.550.575.640 Mucopolysaccharidosis I .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.584 Lipid Metabolism Disorders .
C18.452.584.500 Dyslipidemias .
C18.452.584.500.500 Hyperlipidemias .
C18.452.584.500.500.644 Hyperlipoproteinemias .
C18.452.584.500.500.644.237 Hyperlipoproteinemia Type I .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.202 Carbohydrate Metabolism, Inborn Errors .
C18.452.648.202.715 Mucopolysaccharidoses .
C18.452.648.202.715.640 Mucopolysaccharidosis I .
C18.452.648.398 Lipid Metabolism, Inborn Errors .
C18.452.648.398.465 Hyperlipoproteinemia Type I .
C18.452.648.595 Lysosomal Storage Diseases .
C18.452.648.595.600 Mucopolysaccharidoses .
C18.452.648.595.600.640 Mucopolysaccharidosis I .
C18.452.648.861 Renal Tubular Transport, Inborn Errors .
C18.452.648.861.770 Pseudohypoaldosteronism .
D03 Heterocyclic Compounds .
D03.383 Heterocyclic Compounds, 1-Ring .
D03.383.742 Pyrimidines .
D03.383.742.686 Pyrimidine Nucleotides .
D03.383.742.686.246 Cytosine Nucleotides .
D03.383.742.686.246.400 Cytidine Triphosphate .
D12 Amino Acids, Peptides, and Proteins .
D12.776 Proteins .
D12.776.260 DNA-Binding Proteins .
D12.776.260.108 Basic-Leucine Zipper Transcription Factors .
D12.776.260.108.124 CCAAT-Enhancer-Binding Proteins .
D12.776.260.108.124.750 CCAAT-Enhancer-Binding Protein-beta .
D12.776.660 Nuclear Proteins .
D12.776.660.167 CCAAT-Enhancer-Binding Proteins .
D12.776.660.167.750 CCAAT-Enhancer-Binding Protein-beta .
D12.776.930 Transcription Factors .
D12.776.930.127 Basic-Leucine Zipper Transcription Factors .
D12.776.930.127.124 CCAAT-Enhancer-Binding Proteins .
D12.776.930.127.124.750 CCAAT-Enhancer-Binding Protein-beta .
D13 Nucleic Acids, Nucleotides, and Nucleosides .
D13.695 Nucleotides .
D13.695.740 Pyrimidine Nucleotides .
D13.695.740.246 Cytosine Nucleotides .
D13.695.740.246.400 Cytidine Triphosphate .
D13.695.827 Ribonucleotides .
D13.695.827.232 Cytosine Nucleotides .
D13.695.827.232.400 Cytidine Triphosphate .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
Reflex Sympathetic Dystrophy .
Algodystrophic Syndrome .
CRPS Type I .
Cervical Sympathetic Dystrophy .
Pain Syndrome Type I, Complex Regional .
RSD (Reflex Sympathetic Dystrophy) .
Reflex Sympathetic Dystrophy Syndrome .
Sudek's Atrophy .
Sympathetic Reflex Dystrophia .
Syndrome, Reflex Sympathetic Dystrophy .
Type I Complex Regional Pain Syndrome .
Algodystrophies .
Atrophies, Sudek's .
Atrophy, Sudek .
Atrophy, Sudek's .
CRPS Type Is .
Cervical Sympathetic Dystrophies .
Dystrophies, Cervical Sympathetic .
Dystrophies, Reflex Sympathetic .
Dystrophy, Cervical Sympathetic .
Dystrophy, Reflex Sympathetic .
RSDs (Reflex Sympathetic Dystrophy) .
Reflex Dystrophia, Sympathetic .
Reflex Sympathetic Dystrophies .
Shoulder Hand Syndrome .
Shoulder-Hand Syndromes .
Sudek's Atrophies .
Sudeks Atrophy .
Sympathetic Dystrophies, Cervical .
Sympathetic Dystrophies, Reflex .
Sympathetic Dystrophy, Cervical .
Sympathetic Dystrophy, Reflex .
Sympathetic Reflex Dystrophias .
Syndrome, Algodystrophic .
Syndrome, Shoulder-Hand .
Syndromes, Shoulder-Hand .
Type I, CRPS .
Shoulder-Hand Syndrome .
Sudek Atrophy .
Algodystrophy .
Complex Regional Pain Syndrome, Type I .
Pain Syndrome Type I, Regional, Complex .
SUDECK ATROPHY .
ALGODYSTROPHIC SYNDROME .
SUDECK'S ATROPHY .
1.00
 
Causalgia .
CRPS Type II .
Causalgia Syndrome .
Deafferentation Pain .
Type II Complex Regional Pain Syndrome .
Causalgia Syndromes .
Pain, Deafferentation .
Syndrome, Causalgia .
Syndromes, Causalgia .
Complex Regional Pain Syndrome Type II .
0.75
 
Hyperlipoproteinemia Type I .
Burger-Grutz Syndrome .
C-II Anapolipoproteinemia .
Chylomicronemia, Familial .
Familial Fat-Induced Hypertriglyceridemia .
Familial Hyperchylomicronemia .
Familial Hyperlipoproteinemia Type 1 .
Familial LPL Deficiency .
Familial Lipoprotein Lipase Deficiency .
Hyperlipemia, Essential Familial .
Hyperlipemia, Idiopathic, Burger-Grutz Type .
Hyperlipoproteinemia Type Ia .
Hyperlipoproteinemia Type Ib .
Hyperlipoproteinemia, Type I .
Hyperlipoproteinemia, Type Ia .
Hyperlipoproteinemia, Type Ib .
LIPD Deficiency .
Lipase D Deficiency .
Lipoprotein Lipase Deficiency .
Anapolipoproteinemia, C-II .
Anapolipoproteinemias, C-II .
Apolipoprotein C II Deficiency .
Apolipoprotein C-II Deficiencies .
Burger Grutz Syndrome .
Burger-Grutz Syndromes .
C-II Anapolipoproteinemias .
Chylomicronemias, Familial .
Deficiencies, Apolipoprotein C-II .
Deficiencies, Familial LPL .
Deficiencies, LIPD .
Deficiencies, Lipase D .
Deficiencies, Lipoprotein Lipase .
Deficiency, Apolipoprotein C-II .
Deficiency, Familial LPL .
Deficiency, LIPD .
Deficiency, Lipase D .
Deficiency, Lipoprotein Lipase .
Essential Familial Hyperlipemia .
Essential Familial Hyperlipemias .
Familial Chylomicronemia .
Familial Chylomicronemias .
Familial Fat Induced Hypertriglyceridemia .
Familial Fat-Induced Hypertriglyceridemias .
Familial Hyperchylomicronemias .
Familial Hyperlipemia, Essential .
Familial Hyperlipemias, Essential .
Familial LPL Deficiencies .
Fat-Induced Hypertriglyceridemia, Familial .
Fat-Induced Hypertriglyceridemias, Familial .
Hyperchylomicronemias, Familial .
Hyperlipemias, Essential Familial .
Hyperlipoproteinemia Type Ias .
Hyperlipoproteinemia Type Ibs .
Hyperlipoproteinemia Type Is .
Hyperlipoproteinemias, Type I .
Hyperlipoproteinemias, Type Ia .
Hyperlipoproteinemias, Type Ib .
Hypertriglyceridemia, Familial Fat-Induced .
Hypertriglyceridemias, Familial Fat-Induced .
LIPD Deficiencies .
LPL Deficiencies, Familial .
LPL Deficiency, Familial .
Lipase D Deficiencies .
Lipase Deficiencies, Lipoprotein .
Lipoprotein Lipase Deficiencies .
Syndrome, Burger-Grutz .
Syndromes, Burger-Grutz .
Type I Hyperlipoproteinemia .
Type I Hyperlipoproteinemias .
Type Ia Hyperlipoproteinemia .
Type Ia Hyperlipoproteinemias .
Type Ib Hyperlipoproteinemia .
Type Ib Hyperlipoproteinemias .
Apolipoprotein C-II Deficiency .
Hyperchylomicronemia, Familial .
Lipoprotein Lipase Deficiency, Familial .
0.48
 
Cytidine Triphosphate .
CRPPP .
Magnesium CTP .
Mg CTP .
Triphosphate, Cytidine .
CTP 2791 .
0.47
 
Mucopolysaccharidosis I .
Gargoylism .
Gargoylism, Hurler Syndrome .
Hurler Disease .
Hurler Syndrome .
Hurler's Disease .
Mucopolysaccharidosis 1 .
Mucopolysaccharidosis 5 .
Mucopolysaccharidosis I-S .
Mucopolysaccharidosis Type I .
Mucopolysaccharidosis Type Ih .
Mucopolysaccharidosis Type Ih S .
Mucopolysaccharidosis Type Is .
Scheie Syndrome .
alpha-L-Iduronidase Deficiency .
Disease, Hurler's .
Gargoylisms .
Hurler Scheie Syndrome .
Hurler Syndrome Gargoylism .
Lipochondrodystrophies .
Mucopolysaccharidosis I S .
Mucopolysaccharidosis Is .
Mucopolysaccharidosis Type Ihs .
Syndrome, Hurler's .
Syndrome, Scheie's .
Type Ih, Mucopolysaccharidosis .
Type Ihs, Mucopolysaccharidosis .
alpha L Iduronidase Deficiency .
alpha-L-Iduronidase Deficiencies .
Hurler's Syndrome .
Pfaundler-Hurler Syndrome .
Lipochondrodystrophy .
Hurler-Scheie Syndrome .
Mucopolysaccharidosis V .
Scheie's Syndrome .
GARGOYLISM .
0.43
 
CCAAT-Enhancer-Binding Protein-beta .
23-C-EBP Protein .
40-C-EBP Protein .
AGP-EBP Transcription Factor .
C-EBP beta .
C-EBP-Related Protein 2 .
C-EBPbeta .
CRP2 Protein .
IL-6 DBP .
IL-6-Dependent DNA Binding Protein .
Interleukin-6 Nuclear Factor .
LAP Transcription Factor .
Liver-Enriched Inhibiting Protein .
Liver-Enriched Inhibitory Protein, LIP .
2, C-EBP-Related Protein .
AGP EBP Transcription Factor .
C EBP Related Protein 2 .
C EBP beta .
C EBPbeta .
CCAAT Enhancer Binding Protein beta .
IL 6 Dependent DNA Binding Protein .
Inhibiting Protein, Liver-Enriched .
Interleukin 6 Nuclear Factor .
Liver Enriched Inhibiting Protein .
Liver Enriched Inhibitory Protein, LIP .
Nuclear Factor, Interleukin-6 .
Protein-beta, CCAAT-Enhancer-Binding .
Transcription Factor, AGP-EBP .
Transcription Factor, LAP .
C-EBP-beta .
NF-IL6 .
LIP Protein .
0.41
 
Pseudohypoaldosteronism .
Familial Hyperpotassemia and Hypertension .
Familial Hypertensive Hyperkalemia .
Pseudohypoaldosteronism Type 1, Autosomal Dominant .
Pseudohypoaldosteronism Type 2 .
Pseudohypoaldosteronism Type I .
Pseudohypoaldosteronism Type II .
Familial Hypertensive Hyperkalemias .
Gordon Hyperkalemia Hypertension Syndrome .
Hyperkalemia, Familial Hypertensive .
Hyperkalemia-Hypertension Syndrome, Gordon .
Hyperkalemias, Familial Hypertensive .
Hypertensive Hyperkalemias, Familial .
Pseudohypoaldosteronism Type 1s .
Pseudohypoaldosteronism Type 2s .
Pseudohypoaldosteronism Type IIs .
Pseudohypoaldosteronism Type Is .
Pseudohypoaldosteronisms .
Pseudohypoaldosteronisms, Type I .
Pseudohypoaldosteronisms, Type II .
Syndrome, Gordon Hyperkalemia-Hypertension .
Type 1, Pseudohypoaldosteronism .
Type I Pseudohypoaldosteronism .
Type I, Pseudohypoaldosteronism .
Type II Pseudohypoaldosteronism .
Type II Pseudohypoaldosteronisms .
Type II, Pseudohypoaldosteronism .
Type IIs, Pseudohypoaldosteronism .
Type Is, Pseudohypoaldosteronism .
Gordon Hyperkalemia-Hypertension Syndrome .
Hyperpotassemia and Hypertension, Familial .
Hypertensive Hyperkalemia, Familial .
Pseudohypoaldosteronism Type 1 .
Pseudohypoaldosteronism Type 1, Autosomal Recessive .
Pseudohypoaldosteronism, Type I .
Pseudohypoaldosteronism, Type I, Autosomal Dominant .
Pseudohypoaldosteronism, Type I, Autosomal Recessive .
Pseudohypoaldosteronism, Type II .
0.41