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 .
C10.228.140.163.100.362 Hereditary Central Nervous System Demyelinating Diseases .
C10.228.140.163.100.362.550 Leukodystrophy, Metachromatic .
C10.228.140.163.100.435 Lysosomal Storage Diseases, Nervous System .
C10.228.140.163.100.435.825 Sphingolipidoses .
C10.228.140.163.100.435.825.850 Sulfatidosis .
C10.228.140.163.100.435.825.850.500 Leukodystrophy, Metachromatic .
C10.228.140.300 Cerebrovascular Disorders .
C10.228.140.300.400 Dementia, Vascular .
C10.228.140.300.510 Intracranial Arterial Diseases .
C10.228.140.300.510.800 Intracranial Arteriosclerosis .
C10.228.140.300.510.800.500 Dementia, Vascular .
C10.228.140.380 Dementia .
C10.228.140.380.230 Dementia, Vascular .
C10.228.140.695 Leukoencephalopathies .
C10.228.140.695.500 Dementia, Vascular .
C10.228.140.695.625 Hereditary Central Nervous System Demyelinating Diseases .
C10.228.140.695.625.550 Leukodystrophy, Metachromatic .
C10.314 Demyelinating Diseases .
C10.314.400 Hereditary Central Nervous System Demyelinating Diseases .
C10.314.400.550 Leukodystrophy, Metachromatic .
C14 Cardiovascular Diseases .
C14.907 Vascular Diseases .
C14.907.137 Arterial Occlusive Diseases .
C14.907.137.126 Arteriosclerosis .
C14.907.137.126.372 Intracranial Arteriosclerosis .
C14.907.137.126.372.500 Dementia, Vascular .
C14.907.253 Cerebrovascular Disorders .
C14.907.253.560 Intracranial Arterial Diseases .
C14.907.253.560.350 Intracranial Arteriosclerosis .
C14.907.253.560.350.500 Dementia, Vascular .
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 .
C16.320.565.189.362 Hereditary Central Nervous System Demyelinating Diseases .
C16.320.565.189.362.550 Leukodystrophy, Metachromatic .
C16.320.565.189.435 Lysosomal Storage Diseases, Nervous System .
C16.320.565.189.435.825 Sphingolipidoses .
C16.320.565.189.435.825.850 Sulfatidosis .
C16.320.565.189.435.825.850.500 Leukodystrophy, Metachromatic .
C16.320.565.398 Lipid Metabolism, Inborn Errors .
C16.320.565.398.641 Lipidoses .
C16.320.565.398.641.803 Sphingolipidoses .
C16.320.565.398.641.803.925 Sulfatidosis .
C16.320.565.398.641.803.925.500 Leukodystrophy, Metachromatic .
C16.320.565.595 Lysosomal Storage Diseases .
C16.320.565.595.554 Lysosomal Storage Diseases, Nervous System .
C16.320.565.595.554.825 Sphingolipidoses .
C16.320.565.595.554.825.850 Sulfatidosis .
C16.320.565.595.554.825.850.500 Leukodystrophy, Metachromatic .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.362 Hereditary Central Nervous System Demyelinating Diseases .
C18.452.132.100.362.550 Leukodystrophy, Metachromatic .
C18.452.132.100.435 Lysosomal Storage Diseases, Nervous System .
C18.452.132.100.435.825 Sphingolipidoses .
C18.452.132.100.435.825.850 Sulfatidosis .
C18.452.132.100.435.825.850.500 Leukodystrophy, Metachromatic .
C18.452.584 Lipid Metabolism Disorders .
C18.452.584.687 Lipidoses .
C18.452.584.687.803 Sphingolipidoses .
C18.452.584.687.803.925 Sulfatidosis .
C18.452.584.687.803.925.500 Leukodystrophy, Metachromatic .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.362 Hereditary Central Nervous System Demyelinating Diseases .
C18.452.648.189.362.550 Leukodystrophy, Metachromatic .
C18.452.648.189.435 Lysosomal Storage Diseases, Nervous System .
C18.452.648.189.435.825 Sphingolipidoses .
C18.452.648.189.435.825.850 Sulfatidosis .
C18.452.648.189.435.825.850.500 Leukodystrophy, Metachromatic .
C18.452.648.398 Lipid Metabolism, Inborn Errors .
C18.452.648.398.641 Lipidoses .
C18.452.648.398.641.803 Sphingolipidoses .
C18.452.648.398.641.803.925 Sulfatidosis .
C18.452.648.398.641.803.925.500 Leukodystrophy, Metachromatic .
C18.452.648.595 Lysosomal Storage Diseases .
C18.452.648.595.554 Lysosomal Storage Diseases, Nervous System .
C18.452.648.595.554.825 Sphingolipidoses .
C18.452.648.595.554.825.850 Sulfatidosis .
C18.452.648.595.554.825.850.500 Leukodystrophy, Metachromatic .
F03 Mental Disorders .
F03.615 Neurocognitive Disorders .
F03.615.400 Dementia .
F03.615.400.350 Dementia, Vascular .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
Leukoencephalopathies .
CACH Syndrome .
CACH VWM Syndrome .
Childhood Ataxia with Central Nervous System Hypomyelination .
Childhood Ataxia with Central Nervous System Hypomyelinization .
Cree Leukoencephalopathy .
Myelinosis Centralis Diffusa .
Vanishing White Matter Leukodystrophy .
White Matter Diseases .
CACH Syndromes .
CACH VWM Syndromes .
Centralis Diffusa, Myelinosis .
Centralis Diffusas, Myelinosis .
Cree Leukoencephalopathies .
Diffusa, Myelinosis Centralis .
Diffusas, Myelinosis Centralis .
Disease, White Matter .
Diseases, White Matter .
Leukoencephalopathies, Cree .
Leukoencephalopathy, Cree .
Myelinosis Centralis Diffusas .
Syndrome, CACH .
Syndrome, CACH VWM .
Syndromes, CACH .
Syndromes, CACH VWM .
VWM Syndrome, CACH .
VWM Syndromes, CACH .
White Matter Disease .
Leukoencephalopathy .
Childhood Ataxia with Diffuse Central Nervous System Hypomyelination .
Leukoencephalopathy with Vanishing White Matter .
1.00
191358
 
Dementia, Vascular .
Acute Onset Vascular Dementia .
Arteriosclerotic Encephalopathy, Subcortical .
Binswanger Encephalopathy .
Binswanger's Disease .
Chronic Progressive Subcortical Encephalopathy .
Encephalopathy, Binswanger's .
Encephalopathy, Chronic Progressive Subcortical .
Encephalopathy, Subcortical Arteriosclerotic .
Encephalopathy, Subcortical, Chronic Progressive .
Subcortical Encephalopathy, Chronic Progressive .
Subcortical Leukoencephalopathy .
Subcortical Vascular Dementia .
Vascular Dementia, Acute Onset .
Arteriosclerotic Dementias .
Arteriosclerotic Encephalopathies, Subcortical .
Binswanger's Encephalopathy .
Binswangers Disease .
Dementia, Arteriosclerotic .
Dementia, Subcortical Vascular .
Dementias, Arteriosclerotic .
Dementias, Subcortical Vascular .
Dementias, Vascular .
Disease, Binswanger .
Disease, Binswanger's .
Encephalopathies, Subcortical Arteriosclerotic .
Encephalopathy, Binswangers .
Leukoencephalopathies, Subcortical .
Subcortical Arteriosclerotic Encephalopathies .
Subcortical Leukoencephalopathies .
Subcortical Vascular Dementias .
Vascular Dementia, Subcortical .
Vascular Dementias .
Vascular Dementias, Subcortical .
Arteriosclerotic Dementia .
Vascular Dementia .
Binswanger Disease .
Encephalopathy, Binswanger .
Leukoencephalopathy, Subcortical .
Subcortical Arteriosclerotic Encephalopathy .
0.79
1164431
 
Leukodystrophy, Metachromatic .
ARSA Deficiency .
Arylsulfatase A Deficiency .
Cerebral sclerosis, Diffuse, Metachromatic Form .
Cerebroside Sulfatase Deficiency .
Greenfield Disease .
Greenfield's Disease .
Leukodystrophy, Metachromatic, Adult .
Leukodystrophy, Metachromatic, Juvenile .
Metachromatic Leukodystrophy .
Metachromatic Leukodystrophy, Adult .
Metachromatic Leukodystrophy, Adult-Type .
Metachromatic Leukodystrophy, Infant .
Metachromatic Leukodystrophy, Infant-Type .
Metachromatic Leukodystrophy, Juvenile .
Metachromatic Leukodystrophy, Juvenile-Type .
Metachromatic Leukodystrophy, Late Infantile .
Metachromatic Leukoencephalopathy .
Sulfatide Lipidosis .
ARSA Deficiencies .
Adult Metachromatic Leukodystrophies .
Adult Metachromatic Leukodystrophy .
Adult-Type Metachromatic Leukodystrophies .
Adult-Type Metachromatic Leukodystrophy .
Arylsulfatase A Deficiencies .
Cerebroside Sulfatase Deficiencies .
Deficiencies, ARSA .
Deficiencies, Arylsulfatase A .
Deficiencies, Cerebroside Sulfatase .
Deficiency, ARSA .
Deficiency, Arylsulfatase A .
Deficiency, Cerebroside Sulfatase .
Infant Metachromatic Leukodystrophies .
Infant Metachromatic Leukodystrophy .
Infant-Type Metachromatic Leukodystrophies .
Infant-Type Metachromatic Leukodystrophy .
Juvenile Metachromatic Leukodystrophies .
Juvenile Metachromatic Leukodystrophy .
Juvenile-Type Metachromatic Leukodystrophies .
Juvenile-Type Metachromatic Leukodystrophy .
Leukodystrophies, Adult Metachromatic .
Leukodystrophies, Adult-Type Metachromatic .
Leukodystrophies, Juvenile Metachromatic .
Leukodystrophies, Juvenile-Type Metachromatic .
Leukodystrophies, Metachromatic .
Leukodystrophy, Adult Metachromatic .
Leukodystrophy, Adult-Type Metachromatic .
Leukodystrophy, Juvenile Metachromatic .
Leukodystrophy, Juvenile-Type Metachromatic .
Leukoencephalopathies, Metachromatic .
Leukoencephalopathy, Metachromatic .
Lipidosis, Sulfatide .
Metachromatic Leukodystrophies .
Metachromatic Leukodystrophies, Adult .
Metachromatic Leukodystrophies, Adult-Type .
Metachromatic Leukodystrophies, Infant .
Metachromatic Leukodystrophies, Infant-Type .
Metachromatic Leukodystrophies, Juvenile .
Metachromatic Leukodystrophies, Juvenile-Type .
Metachromatic Leukodystrophy, Adult Type .
Metachromatic Leukodystrophy, Infant Type .
Metachromatic Leukodystrophy, Juvenile Type .
Metachromatic Leukoencephalopathies .
Sulfatase Deficiencies, Cerebroside .
Sulfatase Deficiency, Cerebroside .
Arylsulfatase A Deficiency Disease .
Cerebroside Sulphatase Deficiency Disease .
0.79
151123