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 DeCS Categories

C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
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 .
C10.228.140.252.700.700 Spinocerebellar Ataxias .
C10.228.140.300 Cerebrovascular Disorders .
C10.228.854 Spinal Cord Diseases .
C10.228.854.787 Spinocerebellar Degenerations .
C10.228.854.787.875 Spinocerebellar Ataxias .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.825 Spinocerebellar Degenerations .
C10.574.500.825.700 Spinocerebellar Ataxias .
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 .
C14 Cardiovascular Diseases .
C14.907 Vascular Diseases .
C14.907.253 Cerebrovascular Disorders .
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 .
C16.320.400.780.875 Spinocerebellar Ataxias .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Cerebellar Diseases .
Cerebellar Disorders .
Cerebellar Syndromes .
Cerebellar Disease .
Cerebellar Disorder .
Cerebellar Dysfunctions .
Cerebellar Syndrome .
Cerebellum Disease .
Disease, Cerebellar .
Disease, Cerebellum .
Disorder, Cerebellar .
Dysfunction, Cerebellar .
Syndrome, Cerebellar .
Cerebellar Dysfunction .
Cerebellum Diseases .
Diseases that affect the structure or function of the cerebellum. Cardinal manifestations of cerebellar dysfunction include dysmetria, GAIT ATAXIA, and MUSCLE HYPOTONIA. .
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Cerebrovascular Disorders .
Cerebrovascular Diseases .
Cerebrovascular Insufficiency .
Cerebrovascular Occlusion .
Brain Vascular Disorder .
Cerebrovascular Disease .
Cerebrovascular Disorder .
Cerebrovascular Insufficiencies .
Cerebrovascular Occlusions .
Disease, Cerebrovascular .
Diseases, Cerebrovascular .
Insufficiencies, Cerebrovascular .
Insufficiency, Cerebrovascular .
Intracranial Vascular Disease .
Intracranial Vascular Diseases .
Intracranial Vascular Disorder .
Occlusion, Cerebrovascular .
Occlusions, Cerebrovascular .
Vascular Disease, Intracranial .
Vascular Disorder, Brain .
Vascular Disorder, Intracranial .
Vascular Disorders, Brain .
Vascular Disorders, Intracranial .
Brain Vascular Disorders .
Intracranial Vascular Disorders .
Vascular Diseases, Intracranial .
A spectrum of pathological conditions of impaired blood flow in the brain. They can involve vessels (ARTERIES or VEINS) in the CEREBRUM, the CEREBELLUM, and the BRAIN STEM. Major categories include INTRACRANIAL ARTERIOVENOUS MALFORMATIONS; BRAIN ISCHEMIA; CEREBRAL HEMORRHAGE; and others. .
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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 .
A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43) .
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