serw-MX  [xml]  
 


    
 DeCS Categories

C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.252 Cerebellar Diseases .
C10.228.140.252.700 Spinocerebellar Degenerations .
C10.228.854 Spinal Cord Diseases .
C10.228.854.787 Spinocerebellar Degenerations .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.825 Spinocerebellar Degenerations .
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 .
 
 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. .
1.00
975551
 
Spinocerebellar Degenerations .
Early Onset Cerebellar Ataxia .
Familial Spinocerebellar Degenerations .
Garland-Moorhouse Syndrome .
Hereditary Oligophrenic Cerebello-Lental Degeneration .
Hereditary Spinocerebellar Degenerations .
Inherited Spinocerebellar Degenerations .
Late Onset Cerebellar Ataxia .
Marie's Cerebellar Ataxia .
Marinesco-Garland Syndrome .
Marinesco-Sjogren Syndrome-Hypergonadotrophic Hypogonadism .
Marinesco-Sjogren Syndrome-Myopathy .
Marinesco-Sjogren-Garland Syndrome .
Marinesco-Sjögren Syndrome .
Spino Cerebellar Degenerations .
Spino-Cerebellar Degenerations .
Spinocerebellar Diseases .
Ataxia, Hereditary .
Cerebellar Ataxia, Marie .
Cerebellar Ataxia, Marie's .
Cerebellar Degeneration, Primary .
Corticostriatal Spinal Degeneration .
Corticostriatal-Spinal Degenerations .
Degeneration, Corticostriatal-Spinal .
Degeneration, Familial Spinocerebellar .
Degeneration, Hereditary Spinocerebellar .
Degeneration, Inherited Spinocerebellar .
Degeneration, Primary Cerebellar .
Degeneration, Spino Cerebellar .
Degeneration, Spino-Cerebellar .
Degeneration, Spinocerebellar .
Degenerations, Corticostriatal-Spinal .
Degenerations, Familial Spinocerebellar .
Degenerations, Hereditary Spinocerebellar .
Degenerations, Inherited Spinocerebellar .
Degenerations, Primary Cerebellar .
Degenerations, Spino Cerebellar .
Degenerations, Spinocerebellar .
Familial Spinocerebellar Degeneration .
Garland Moorhouse Syndrome .
Hereditary Ataxia .
Hereditary Ataxias .
Hereditary Oligophrenic Cerebello Lental Degeneration .
Hereditary Spinocerebellar Degeneration .
Hypogonadism, Marinesco-Sjogren Syndrome-Hypergonadotrophic .
Inherited Spinocerebellar Degeneration .
Marinesco Garland Syndrome .
Marinesco Sjogren Garland Syndrome .
Marinesco Sjogren Syndrome .
Marinesco Sjogren Syndrome Hypergonadotrophic Hypogonadism .
Marinesco Sjogren Syndrome Myopathy .
Marinesco Sjögren Syndrome .
Primary Cerebellar Degeneration .
Primary Cerebellar Degenerations .
Spino Cerebellar Degeneration .
Spino-Cerebellar Degeneration .
Spinocerebellar Degeneration, Familial .
Spinocerebellar Degeneration, Hereditary .
Spinocerebellar Degeneration, Inherited .
Spinocerebellar Degenerations, Familial .
Spinocerebellar Degenerations, Hereditary .
Spinocerebellar Degenerations, Inherited .
Spinocerebellar Disease .
Syndrome, Garland-Moorhouse .
Syndrome, Marinesco-Garland .
Syndrome, Marinesco-Sjogren .
Syndrome, Marinesco-Sjogren-Garland .
Syndrome, Marinesco-Sjögren .
Syndrome-Hypergonadotrophic Hypogonadism, Marinesco-Sjogren .
Syndrome-Myopathy, Marinesco-Sjogren .
Ataxias, Hereditary .
Marinesco-Sjogren Syndrome .
Spinocerebellar Degeneration .
Cerebellar Ataxia, Early Onset .
Cerebellar Ataxia, Late Onset .
Cerebellar Degenerations, Primary .
Corticostriatal-Spinal Degeneration .
Marie Cerebellar Ataxia .
A heterogenous group of degenerative syndromes marked by progressive cerebellar dysfunction either in isolation or combined with other neurologic manifestations. Sporadic and inherited subtypes occur. Inheritance patterns include autosomal dominant, autosomal recessive, and X-linked. .
0.69
321699