DeCS Inglês

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 .
C10.228.140.163.100.435.825.300 Gangliosidoses .
C10.228.140.163.100.435.825.300.300 Gangliosidoses, GM2 .
C10.228.140.163.100.435.825.300.300.500 Tay-Sachs Disease .
C10.228.140.163.100.435.825.700 Niemann-Pick Diseases .
C10.228.140.163.100.435.825.700.500 Niemann-Pick Disease, Type A .
C15 Hemic and Lymphatic Diseases .
C15.604 Lymphatic Diseases .
C15.604.250 Histiocytosis .
C15.604.250.410 Histiocytosis, Non-Langerhans-Cell .
C15.604.250.410.625 Niemann-Pick Diseases .
C15.604.250.410.625.500 Niemann-Pick Disease, Type A .
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 .
C16.320.565.189.435.825.300 Gangliosidoses .
C16.320.565.189.435.825.300.300 Gangliosidoses, GM2 .
C16.320.565.189.435.825.300.300.500 Tay-Sachs Disease .
C16.320.565.189.435.825.700 Niemann-Pick Diseases .
C16.320.565.189.435.825.700.500 Niemann-Pick Disease, Type A .
C16.320.565.398 Lipid Metabolism, Inborn Errors .
C16.320.565.398.641 Lipidoses .
C16.320.565.398.641.803 Sphingolipidoses .
C16.320.565.398.641.803.350 Gangliosidoses .
C16.320.565.398.641.803.350.300 Gangliosidoses, GM2 .
C16.320.565.398.641.803.350.300.850 Tay-Sachs Disease .
C16.320.565.398.641.803.730 Niemann-Pick Diseases .
C16.320.565.398.641.803.730.500 Niemann-Pick Disease, Type A .
C16.320.565.595 Lysosomal Storage Diseases .
C16.320.565.595.554 Lysosomal Storage Diseases, Nervous System .
C16.320.565.595.554.825 Sphingolipidoses .
C16.320.565.595.554.825.300 Gangliosidoses .
C16.320.565.595.554.825.300.300 Gangliosidoses, GM2 .
C16.320.565.595.554.825.300.300.840 Tay-Sachs Disease .
C16.320.565.595.554.825.700 Niemann-Pick Diseases .
C16.320.565.595.554.825.700.500 Niemann-Pick Disease, Type A .
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 .
C18.452.132.100.435.825.300 Gangliosidoses .
C18.452.132.100.435.825.300.300 Gangliosidoses, GM2 .
C18.452.132.100.435.825.300.300.500 Tay-Sachs Disease .
C18.452.132.100.435.825.700 Niemann-Pick Diseases .
C18.452.132.100.435.825.700.500 Niemann-Pick Disease, Type A .
C18.452.584 Lipid Metabolism Disorders .
C18.452.584.687 Lipidoses .
C18.452.584.687.803 Sphingolipidoses .
C18.452.584.687.803.350 Gangliosidoses .
C18.452.584.687.803.350.300 Gangliosidoses, GM2 .
C18.452.584.687.803.350.300.850 Tay-Sachs Disease .
C18.452.584.687.803.730 Niemann-Pick Diseases .
C18.452.584.687.803.730.500 Niemann-Pick Disease, Type A .
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 .
C18.452.648.189.435.825.300 Gangliosidoses .
C18.452.648.189.435.825.300.300 Gangliosidoses, GM2 .
C18.452.648.189.435.825.300.300.500 Tay-Sachs Disease .
C18.452.648.189.435.825.700 Niemann-Pick Diseases .
C18.452.648.189.435.825.700.500 Niemann-Pick Disease, Type A .
C18.452.648.398 Lipid Metabolism, Inborn Errors .
C18.452.648.398.641 Lipidoses .
C18.452.648.398.641.803 Sphingolipidoses .
C18.452.648.398.641.803.350 Gangliosidoses .
C18.452.648.398.641.803.350.300 Gangliosidoses, GM2 .
C18.452.648.398.641.803.350.300.850 Tay-Sachs Disease .
C18.452.648.398.641.803.730 Niemann-Pick Diseases .
C18.452.648.398.641.803.730.500 Niemann-Pick Disease, Type A .
C18.452.648.595 Lysosomal Storage Diseases .
C18.452.648.595.554 Lysosomal Storage Diseases, Nervous System .
C18.452.648.595.554.825 Sphingolipidoses .
C18.452.648.595.554.825.300 Gangliosidoses .
C18.452.648.595.554.825.300.300 Gangliosidoses, GM2 .
C18.452.648.595.554.825.300.300.840 Tay-Sachs Disease .
C18.452.648.595.554.825.700 Niemann-Pick Diseases .
C18.452.648.595.554.825.700.500 Niemann-Pick Disease, Type A .
D09 Carbohydrates .
D09.400 Glycoconjugates .
D09.400.410 Glycolipids .
D09.400.410.420 Glycosphingolipids .
D10 Lipids .
D10.390 Glycolipids .
D10.390.470 Glycosphingolipids .
D10.570 Membrane Lipids .
D10.570.877 Sphingolipids .
D10.570.877.360 Glycosphingolipids .

Termos
Sinônimos e Históricos

Documentos
LILACS e MDL

Sphingolipidoses .
Sphingolipid Storage Diseases .
Sphingolipidosis .
Sphingolipid Storage Disease .
Storage Disease, Sphingolipid .
Storage Diseases, Sphingolipid .
1.00

Sphingolipids .
Lysosphingolipids .
0.85

Niemann-Pick Disease, Type A .
Classical Niemann-Pick Disease .
Neuronal Cholesterol Lipidosis .
Niemann-Pick Disease, Acute Neuronopathic Form .
Niemann-Pick Disease, Acute Neurovisceral Form .
Niemann-Pick Disease, Neuronopathic Type .
Niemann-Pick's Disease Type A .
Ophthalmoplegia, Supraoptic Vertical .
Sphingomyelin Cholesterol Lipidosis .
Sphingomyelin Lipidosis .
Sphingomyelinase Deficiency .
Type A Niemann-Pick Disease .
Cholesterol Lipidoses, Neuronal .
Cholesterol Lipidoses, Sphingomyelin .
Cholesterol Lipidosis, Neuronal .
Cholesterol Lipidosis, Sphingomyelin .
Classical Niemann Pick Disease .
Deficiencies, Sphingomyelinase .
Deficiency, Sphingomyelinase .
Lipidoses, Neuronal Cholesterol .
Lipidoses, Sphingomyelin .
Lipidoses, Sphingomyelin Cholesterol .
Lipidosis, Neuronal Cholesterol .
Lipidosis, Sphingomyelin .
Lipidosis, Sphingomyelin Cholesterol .
Neuronal Cholesterol Lipidoses .
Niemann Pick Disease, Acute Neuronopathic Form .
Niemann Pick Disease, Acute Neurovisceral Form .
Niemann Pick Disease, Neuronopathic Type .
Niemann Pick Disease, Type A .
Niemann Pick's Disease Type A .
Niemann-Pick Disease, Classical .
Ophthalmoplegias, Supraoptic Vertical .
Sphingomyelin Cholesterol Lipidoses .
Sphingomyelin Lipidoses .
Sphingomyelinase Deficiencies .
Sphingomyelinase Deficiency Diseases .
Supraoptic Vertical Ophthalmoplegia .
Supraoptic Vertical Ophthalmoplegias .
Type A Niemann Pick Disease .
Vertical Ophthalmoplegia, Supraoptic .
Vertical Ophthalmoplegias, Supraoptic .
Sphingomyelinase Deficiency Disease .
Classical Niemann-Pick Disease .
0.72

Tay-Sachs Disease .
Amaurotic Familial Idiocy .
B Variant GM2 Gangliosidosis .
B Variant GM2-Gangliosidosis .
Deficiency Disease Hexosaminidase A .
Familial Amaurotic Idiocy .
GM2 Gangliosidosis, B Variant .
GM2 Gangliosidosis, Type 1 .
GM2 Gangliosidosis, Type I .
GM2-Gangliosidosis, Type I .
Gangliosidosis GM2 , Type 1 .
Gangliosidosis GM2, Type I .
HexA Deficiency .
Hexosaminidase A Deficiency .
Hexosaminidase alpha-Subunit Deficiency (Variant B) .
Sphingolipidosis, Tay-Sachs .
Amaurotic Idiocy, Familial .
B Variant GM2-Gangliosidoses .
Deficiency, Hexosaminidase A .
Deficiency, Hexosaminidase alpha-Subunit (Variant B) .
GM2-Gangliosidosis, B Variant .
Hexosaminidase alpha Subunit Deficiency (Variant B) .
Sphingolipidosis, Tay Sachs .
Tay Sachs Disease .
Tay Sachs Disease, B Variant .
Tay-Sachs Sphingolipidosis .
Type I GM2-Gangliosidosis .
Gangliosidosis G(M2), Type I .
G(M2) Gangliosidosis, Type I .
Gangliosidosis GM2, B Variant .
Hexosaminidase A Deficiency Disease .
Tay-Sachs Disease, B Variant .
Amaurotic Familial Idiocy .
Gangliosidosis GM2, Type I .
0.66

Glycosphingolipids .
Asialogangliosides .
Sphingoglycolipids .
0.66