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 .
C10.228.140.163.100.435 Lysosomal Storage Diseases, Nervous System .
C10.228.140.163.100.435.825 Sphingolipidoses .
C10.228.140.163.100.435.825.400 Gaucher Disease .
C10.668 Neuromuscular Diseases .
C10.668.829 Peripheral Nervous System Diseases .
C10.668.829.800 Polyneuropathies .
C10.668.829.800.875 Tangier Disease .
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 .
C16.320.565.189.435 Lysosomal Storage Diseases, Nervous System .
C16.320.565.189.435.825 Sphingolipidoses .
C16.320.565.189.435.825.400 Gaucher Disease .
C16.320.565.398 Lipid Metabolism, Inborn Errors .
C16.320.565.398.500 Hypolipoproteinemias .
C16.320.565.398.500.330 Hypoalphalipoproteinemias .
C16.320.565.398.500.330.750 Tangier Disease .
C16.320.565.398.641 Lipidoses .
C16.320.565.398.641.803 Sphingolipidoses .
C16.320.565.398.641.803.441 Gaucher Disease .
C16.320.565.595 Lysosomal Storage Diseases .
C16.320.565.595.554 Lysosomal Storage Diseases, Nervous System .
C16.320.565.595.554.825 Sphingolipidoses .
C16.320.565.595.554.825.400 Gaucher Disease .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.435 Lysosomal Storage Diseases, Nervous System .
C18.452.132.100.435.825 Sphingolipidoses .
C18.452.132.100.435.825.400 Gaucher Disease .
C18.452.584 Lipid Metabolism Disorders .
C18.452.584.500 Dyslipidemias .
C18.452.584.500.875 Hypolipoproteinemias .
C18.452.584.500.875.330 Hypoalphalipoproteinemias .
C18.452.584.500.875.330.750 Tangier Disease .
C18.452.584.687 Lipidoses .
C18.452.584.687.803 Sphingolipidoses .
C18.452.584.687.803.441 Gaucher Disease .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.435 Lysosomal Storage Diseases, Nervous System .
C18.452.648.189.435.825 Sphingolipidoses .
C18.452.648.189.435.825.400 Gaucher Disease .
C18.452.648.398 Lipid Metabolism, Inborn Errors .
C18.452.648.398.500 Hypolipoproteinemias .
C18.452.648.398.500.330 Hypoalphalipoproteinemias .
C18.452.648.398.500.330.750 Tangier Disease .
C18.452.648.398.641 Lipidoses .
C18.452.648.398.641.803 Sphingolipidoses .
C18.452.648.398.641.803.441 Gaucher Disease .
C18.452.648.595 Lysosomal Storage Diseases .
C18.452.648.595.554 Lysosomal Storage Diseases, Nervous System .
C18.452.648.595.554.825 Sphingolipidoses .
C18.452.648.595.554.825.400 Gaucher Disease .
L01 Information Science .
L01.453 Information Services .
L01.453.245 Documentation .
L01.453.245.945 Vocabulary, Controlled .
SP4 Environmental Health .
SP4.011 Science .
SP4.011.127 Social Sciences .
SP4.011.127.428 Information Science .
SP4.011.127.428.809 Vocabulary, Controlled .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
Metabolic Diseases .
Diseases, Metabolic .
Disease, Metabolic .
Metabolic Disease .
Thesaurismoses .
Thesaurismosis .
1.00
4429686
 
Vocabulary, Controlled .
Controlled Thesauri .
Controlled Thesaurus .
Thesauri .
Controlled Vocabularies .
Thesauri, Controlled .
Thesaurus, Controlled .
Vocabularies, Controlled .
Controlled Vocabulary .
Thesaurus .
Thesauri .
0.79
483292
 
Gaucher Disease .
Acid beta-Glucosidase Deficiency .
Acid beta-Glucosidase Deficiency Disease .
Acute Neuronopathic Gaucher Disease .
Chronic Gaucher Disease .
GBA Deficiency .
Gaucher Disease Type 3 .
Gaucher Disease, Acute Neuronopathic .
Gaucher Disease, Acute Neuronopathic Type .
Gaucher Disease, Chronic .
Gaucher Disease, Chronic Neuronopathic Type .
Gaucher Disease, Infantile .
Gaucher Disease, Infantile Cerebral .
Gaucher Disease, Juvenile .
Gaucher Disease, Juvenile and Adult, Cerebral .
Gaucher Disease, Neuronopathic .
Gaucher Disease, Non-Neuronopathic Form .
Gaucher Disease, Noncerebral Juvenile .
Gaucher Disease, Subacute Neuronopathic Form .
Gaucher Disease, Subacute Neuronopathic Type .
Gaucher Disease, Type 1 .
Gaucher Disease, Type 2 .
Gaucher Disease, Type 3 .
Gaucher Disease, Type I .
Gaucher Disease, Type II .
Gaucher Disease, Type III .
Gaucher Splenomegaly .
Gaucher Syndrome .
Gaucher's Disease .
Gauchers Disease .
Glucocerebrosidase Deficiency .
Glucocerebrosidosis .
Glucosyl Cerebroside Lipidosis .
Glucosylceramidase Deficiency .
Glucosylceramide Beta-Glucosidase Deficiency .
Glucosylceramide Lipidosis .
Infantile Gaucher Disease .
Kerasin Histiocytosis .
Kerasin Lipoidosis .
Kerasin thesaurismosis .
Lipoid Histiocytosis (Kerasin Type) .
Non-Neuronopathic Gaucher Disease .
Subacute Neuronopathic Gaucher Disease .
Type 1 Gaucher Disease .
Type 2 Gaucher Disease .
Type 3 Gaucher Disease .
Cerebroside Lipidoses, Glucosyl .
Cerebroside Lipidosis Syndromes .
Cerebroside Lipidosis, Glucosyl .
Deficiencies, GBA .
Deficiencies, Glucocerebrosidase .
Deficiency Disease, Glucocerebrosidase .
Deficiency Diseases, Glucocerebrosidase .
Deficiency, GBA .
Deficiency, Glucocerebrosidase .
Disease, Chronic Gaucher .
Disease, Gaucher .
Disease, Gaucher's .
Disease, Gauchers .
Disease, Glucocerebrosidase Deficiency .
Disease, Infantile Gaucher .
Disease, Juvenile Gaucher .
Disease, Neuronopathic Gaucher .
Disease, Non-Neuronopathic Gaucher .
Diseases, Gauchers .
Diseases, Glucocerebrosidase Deficiency .
GBA Deficiencies .
Gaucher Disease, Non Neuronopathic Form .
Gaucher Disease, Non-Neuronopathic .
Gauchers Diseases .
Glucocerebrosidase Deficiencies .
Glucocerebrosidase Deficiency Diseases .
Glucocerebrosidoses .
Glucosyl Cerebroside Lipidoses .
Glucosylceramide Lipidoses .
Histiocytoses, Kerasin .
Histiocytoses, Lipoid (Kerasin Type) .
Histiocytosis, Kerasin .
Histiocytosis, Lipoid (Kerasin Type) .
Juvenile Gaucher Disease .
Kerasin Histiocytoses .
Kerasin Lipoidoses .
Kerasin thesaurismoses .
Lipidoses, Glucosyl Cerebroside .
Lipidoses, Glucosylceramide .
Lipidosis Syndrome, Cerebroside .
Lipidosis Syndromes, Cerebroside .
Lipidosis, Glucosyl Cerebroside .
Lipidosis, Glucosylceramide .
Lipoid Histiocytoses (Kerasin Type) .
Lipoidoses, Kerasin .
Lipoidosis, Kerasin .
Non Neuronopathic Gaucher Disease .
Splenomegaly, Gaucher .
Syndrome, Cerebroside Lipidosis .
Syndrome, Gaucher .
Syndromes, Cerebroside Lipidosis .
thesaurismoses, Kerasin .
thesaurismosis, Kerasin .
Cerebroside Lipidosis Syndrome .
Glucocerebrosidase Deficiency Disease .
Glucosylceramide Beta-Glucosidase Deficiency Disease .
Neuronopathic Gaucher Disease .
Gaucher Disease Type 1 .
Gaucher Disease Type 2 .
GAUCHER'S DISEASE .
0.78
873964
 
Tangier Disease .
Alpha High Density Lipoprotein Deficiency Disease .
Cholesterol Thesaurismosis .
HDLDT1 .
High Density Lipoprotein Deficiency, Tangier Type .
High Density Lipoprotein Deficiency, Type 1 .
High-Density Lipoprotein Deficiency, Tangier Type .
High-Density Lipoprotein Deficiency, Type I .
Neuropathy of Tangier Disease .
Tangier Hereditary Neuropathy .
A-alphalipoprotein Neuropathies .
Analphalipoproteinemias .
Cholesterol Thesaurismoses .
High Density Lipoprotein Deficiency, Type I .
Neuropathies, A-alphalipoprotein .
Neuropathy, A-alphalipoprotein .
Thesaurismoses, Cholesterol .
Thesaurismosis, Cholesterol .
Analphalipoproteinemia .
A-alphalipoprotein Neuropathy .
Tangier Disease Neuropathy .
0.76
3491