serw-MX  [xml]  
 


    
 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 .
C10.228.140.252.700 Spinocerebellar Degenerations .
C10.228.140.252.700.650 Olivopontocerebellar Atrophies .
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 .
C10.500 Nervous System Malformations .
C10.500.300 Hereditary Sensory and Motor Neuropathy .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.495 Hereditary Sensory and Motor Neuropathy .
C10.574.500.825 Spinocerebellar Degenerations .
C10.574.500.825.650 Olivopontocerebellar Atrophies .
C10.574.625 Multiple System Atrophy .
C10.574.625.600 Olivopontocerebellar Atrophies .
C10.668 Neuromuscular Diseases .
C10.668.829 Peripheral Nervous System Diseases .
C10.668.829.800 Polyneuropathies .
C10.668.829.800.300 Hereditary Sensory and Motor Neuropathy .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.666 Nervous System Malformations .
C16.131.666.300 Hereditary Sensory and Motor Neuropathy .
C16.320 Genetic Diseases, Inborn .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.375 Hereditary Sensory and Motor Neuropathy .
C16.320.400.780 Spinocerebellar Degenerations .
C16.320.400.780.750 Olivopontocerebellar Atrophies .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
Hereditary Sensory and Motor Neuropathy .
CMT4f .
Charcot-Marie-Tooth Disease, Demyelinating, Type 4f .
Charcot-Marie-Tooth Disease, Type 3 .
Dejerine-Sottas Neuropathy .
Dejerine-Sottas Syndrome .
HMSN3 .
Herditary Sensory and Motor Neuropathy .
Hereditary Motor and Sensory Neuropathy .
Hereditary Motor and Sensory Neuropathy 3 .
Hereditary Motor and Sensory Neuropathy Type III .
Hypertrophic Neuropathy of Dejerine-Sottas .
Charcot Marie Tooth Disease, Type 3 .
Dejerine Sottas Disease .
Dejerine Sottas Neuropathy .
Dejerine Sottas Syndrome .
Dejerine-Sottas Hypertrophic Neuropathy .
Disease, Dejerine-Sottas .
HMSN Type IIIs .
HMSN Type VIIs .
Hypertrophic Neuropathy of Dejerine Sottas .
Neuropathy, Dejerine-Sottas .
Syndrome, Dejerine-Sottas .
Type VII, HMSN .
Hereditary Motor and Sensory Neuropathies .
Dejerine-Sottas Disease .
HMSN 13329 .
HMSN Type III .
HMSN Type VII .
Neuropathies, Hereditary Motor and Sensory .
Hereditary, Type III, Motor and Sensory Neuropathy .
Hereditary, Type VII, Motor and Sensory Neuropathy .
HEREDIATARY, TYPE VII, MOTOR AND SENSORY NEUROPATHY .
1.00
 
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 .
0.67