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 Categorias DeCS

C10 Nervous System Diseases .
C10.177 Autonomic Nervous System Diseases .
C10.177.575 Primary Dysautonomias .
C10.177.575.550 Multiple System Atrophy .
C10.177.575.550.375 Olivopontocerebellar Atrophies .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.079 Basal Ganglia Diseases .
C10.228.140.079.612 Multiple System Atrophy .
C10.228.140.079.612.600 Olivopontocerebellar Atrophies .
C10.228.140.252 Cerebellar Diseases .
C10.228.140.252.190 Cerebellar Ataxia .
C10.228.140.252.190.530 Spinocerebellar Ataxias .
C10.228.140.252.700 Spinocerebellar Degenerations .
C10.228.140.252.700.650 Olivopontocerebellar Atrophies .
C10.228.140.252.700.700 Spinocerebellar Ataxias .
C10.228.662 Movement Disorders .
C10.228.662.550 Multiple System Atrophy .
C10.228.662.550.600 Olivopontocerebellar Atrophies .
C10.228.854 Spinal Cord Diseases .
C10.228.854.787 Spinocerebellar Degenerations .
C10.228.854.787.750 Olivopontocerebellar Atrophies .
C10.228.854.787.875 Spinocerebellar Ataxias .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.825 Spinocerebellar Degenerations .
C10.574.500.825.650 Olivopontocerebellar Atrophies .
C10.574.500.825.700 Spinocerebellar Ataxias .
C10.574.625 Multiple System Atrophy .
C10.574.625.600 Olivopontocerebellar Atrophies .
C10.597 Neurologic Manifestations .
C10.597.350 Dyskinesias .
C10.597.350.090 Ataxia .
C10.597.350.090.500 Cerebellar Ataxia .
C10.597.350.090.500.530 Spinocerebellar Ataxias .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.780 Spinocerebellar Degenerations .
C16.320.400.780.750 Olivopontocerebellar Atrophies .
C16.320.400.780.875 Spinocerebellar Ataxias .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
Olivopontocerebellar Atrophies .
Familial Olivopontocerebellar Atrophy .
Inherited Olivopontocerebellar Atrophy .
Nonfamilial Olivopontocerebellar Atrophy .
Olivo-Ponto-Cerebellar Atrophy .
Olivo-Ponto-Cerebellar Degeneration .
Olivopontocerebellar Atrophy .
Olivopontocerebellar Degeneration .
Pontoolivocerebellar Atrophy .
Presenile Ataxia .
Ataxia, Presenile .
Ataxias, Presenile .
Atrophy, Familial Olivopontocerebellar .
Atrophy, Idiopathic Olivopontocerebellar .
Atrophy, Inherited Olivopontocerebellar .
Atrophy, Nonfamilial Olivopontocerebellar .
Atrophy, Olivo-Ponto-Cerebellar .
Atrophy, Olivopontocerebellar .
Atrophy, Pontoolivocerebellar .
Degeneration, Olivo-Ponto-Cerebellar .
Degeneration, Olivopontocerebellar .
Degenerations, Olivo-Ponto-Cerebellar .
Degenerations, Olivopontocerebellar .
Dejerine Thomas Syndrome .
Familial Olivopontocerebellar Atrophies .
Idiopathic Olivopontocerebellar Atrophies .
Idiopathic Olivopontocerebellar Atrophy .
Inherited Olivopontocerebellar Atrophies .
Nonfamilial Olivopontocerebellar Atrophies .
Olivo Ponto Cerebellar Atrophy .
Olivo Ponto Cerebellar Degeneration .
Olivo-Ponto-Cerebellar Degenerations .
Olivopontocerebellar Atrophies, Familial .
Olivopontocerebellar Atrophies, Idiopathic .
Olivopontocerebellar Atrophies, Inherited .
Olivopontocerebellar Atrophies, Nonfamilial .
Olivopontocerebellar Atrophy, Familial .
Olivopontocerebellar Atrophy, Inherited .
Olivopontocerebellar Atrophy, Nonfamilial .
Olivopontocerebellar Degenerations .
Pontoolivocerebellar Atrophies .
Presenile Ataxias .
Syndrome, Dejerine-Thomas .
Dejerine-Thomas Syndrome .
Olivopontocerebellar Atrophy, Idiopathic .
OLIVOPONTOCEREBELLAR DEGENERATION .
OLIVOPONTOCEREBELLAR ATROPHY .
1.00
 
Spinocerebellar Ataxias .
Autosomal Dominant Cerebellar Ataxia, Type II .
Cerebellar Degeneration with Slow Eye Movements .
Cerebelloparenchymal Disorder I .
Dominantly-Inherited Spinocerebellar Ataxias .
Menzel Type OPCA .
OPCA with Macular Degeneration and External Ophthalmoplegia .
OPCA with Retinal Degeneration .
Olivopontocerebellar Atrophy 2 .
Olivopontocerebellar Atrophy I .
Olivopontocerebellar Atrophy II .
Olivopontocerebellar Atrophy III .
Olivopontocerebellar Atrophy IV .
Olivopontocerebellar Atrophy, Holguin Type .
SCA1 22058 .
Schut-Haymaker Type OPCA .
Spinocerebellar Ataxia 1 .
Spinocerebellar Ataxia 2 .
Spinocerebellar Ataxia 4 .
Spinocerebellar Ataxia 5 .
Spinocerebellar Ataxia 6 .
Spinocerebellar Ataxia 7 .
Spinocerebellar Ataxia with Slow Eye Movements .
Spinocerebellar Ataxia, Autosomal Dominant, with Sensory Axonal Neuropathy .
Spinocerebellar Ataxia, Cuban Type .
Spinocerebellar Ataxia-1 .
Spinocerebellar Ataxia-2 .
Spinocerebellar Ataxia-4 .
Spinocerebellar Ataxia-5 .
Spinocerebellar Ataxia-6 .
Spinocerebellar Ataxia-7 .
Spinocerebellar Ataxias, Dominantly-Inherited .
Spinocerebellar Atrophy 2 .
Spinocerebellar Atrophy I .
Spinocerebellar Atrophy II .
Spinocerebellar Degeneration with Slow Eye Movements .
Type 1 Spinocerebellar Ataxia .
Type 2 Spinocerebellar Ataxia .
Type 4 Spinocerebellar Ataxia .
Type 5 Spinocerebellar Ataxia .
Type 6 Spinocerebellar Ataxia .
Type 7 Spinocerebellar Ataxia .
Wadia Swami Syndrome .
Wadia-Swami Syndrome .
Ataxia 1, Spinocerebellar .
Ataxia 2, Spinocerebellar .
Ataxia 2s, Spinocerebellar .
Ataxia 4, Spinocerebellar .
Ataxia 4s, Spinocerebellar .
Ataxia 5, Spinocerebellar .
Ataxia 5s, Spinocerebellar .
Ataxia 6, Spinocerebellar .
Ataxia 6s, Spinocerebellar .
Ataxia 7, Spinocerebellar .
Ataxia 7s, Spinocerebellar .
Ataxia, Dominantly-Inherited Spinocerebellar .
Ataxia, Spinocerebellar .
Ataxias, Dominantly-Inherited Spinocerebellar .
Ataxias, Spinocerebellar .
Atrophies, Spinocerebellar .
Atrophy 2, Olivopontocerebellar .
Atrophy 2, Spinocerebellar .
Atrophy 2s, Olivopontocerebellar .
Atrophy 2s, Spinocerebellar .
Atrophy I, Olivopontocerebellar .
Atrophy I, Spinocerebellar .
Atrophy II, Olivopontocerebellar .
Atrophy II, Spinocerebellar .
Atrophy III, Olivopontocerebellar .
Atrophy IIs, Olivopontocerebellar .
Atrophy IIs, Spinocerebellar .
Atrophy IV, Olivopontocerebellar .
Atrophy IVs, Olivopontocerebellar .
Atrophy, Spinocerebellar .
Cerebelloparenchymal Disorder Is .
Dominantly Inherited Spinocerebellar Ataxias .
Dominantly-Inherited Spinocerebellar Ataxia .
II, Olivopontocerebellar Atrophy .
II, Spinocerebellar Atrophy .
IIs, Olivopontocerebellar Atrophy .
IIs, Spinocerebellar Atrophy .
OPCA, Menzel Type .
OPCA, Schut-Haymaker Type .
Olivopontocerebellar Atrophy 2s .
Olivopontocerebellar Atrophy IIIs .
Olivopontocerebellar Atrophy IIs .
Olivopontocerebellar Atrophy IVs .
Olivopontocerebellar Atrophy Is .
SCA1s .
Schut Haymaker Type OPCA .
Spinocerebellar Ataxia .
Spinocerebellar Ataxia 1s .
Spinocerebellar Ataxia 2s .
Spinocerebellar Ataxia 4s .
Spinocerebellar Ataxia 5s .
Spinocerebellar Ataxia 6s .
Spinocerebellar Ataxia 7s .
Spinocerebellar Ataxia, Dominantly-Inherited .
Spinocerebellar Ataxias, Dominantly Inherited .
Spinocerebellar Atrophy .
Spinocerebellar Atrophy 2s .
Spinocerebellar Atrophy IIs .
Spinocerebellar Atrophy Is .
Swami Syndrome, Wadia .
Syndrome, Wadia Swami .
Syndrome, Wadia-Swami .
Spinocerebellar Ataxia Type 1 .
Spinocerebellar Ataxia Type 2 .
Spinocerebellar Ataxia Type 4 .
Spinocerebellar Ataxia Type 5 .
Spinocerebellar Ataxia Type 6 .
Spinocerebellar Ataxia Type 7 .
Spinocerebellar Atrophies .
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