Spinocerebellar Degenerations [spinocerebelární degenerace]

topical
30
Terms

cerebelární ataxie s pozdním nástupem
cerebelární ataxie s raným nástupem
cerebelární ataxie, pozdní nástup
cerebelární ataxie, raný nástup
dědičné ataxie
dědičné spinocerebelární degenerace
kortikostriatálně-spinální degenerace
Marieova cerebelární ataxie
Marieova hereditární ataxie
Marinesco Sjogren syndrom
Marinesco-Sjogren syndrom
primární cerebelární degenerace

 

Ataxias, Hereditary
Cerebellar Ataxia, Early Onset
Cerebellar Ataxia, Late Onset
Cerebellar Degenerations, Primary
Corticostriatal-Spinal Degeneration
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 Cerebellar Ataxia
Marie's Cerebellar Ataxia
Marinesco-Garland Syndrome
Marinesco-Sjogren Syndrome
Marinesco-Sjögren Syndrome
Marinesco-Sjogren Syndrome-Hypergonadotrophic Hypogonadism
Marinesco-Sjogren Syndrome-Myopathy
Marinesco-Sjogren-Garland Syndrome
Spino Cerebellar Degenerations
Spino-Cerebellar Degenerations
Spinocerebellar Degeneration
Spinocerebellar Diseases

Persistent link   https://www.medvik.cz/link/D013132
Definition

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.

DUI
D013132 MeSH Browser
CUI
M0020336
Previous indexing
Cerebellar Ataxia (1968-1986); Cerebellar Diseases (1966-1986); Spinal Cord Diseases (1966-1986)
History note
2000(1987)
Public note
2000; see SPINOCEREBELLAR DEGENERATION 1989-1999, see SPINOCEREBELLAR DEGENERATIONS 1987-1988

C Diseases
C10.228.140 Brain Diseases 1 178
C10.228.140.252 Cerebellar Diseases 165
C10.228.140.252.190 Cerebellar Ataxia 63
C10.228.140.252.200 Cerebellar Neoplasms 65
C10.228.140.252.300 Dandy-Walker Syndrome 6
C10.228.140.252.500 Miller Fisher Syndrome 12
C10.228.140.252.700 Spinocerebellar Degenerations 30
C10.228.140.252.700.150 Friedreich Ataxia 54
C10.228.140.252.700.250 Myoclonic Cerebellar Dyssynergia
C10.228.140.252.700.650 Olivopontocerebellar Atrophies 21
C10.228.140.252.700.700 Spinocerebellar Ataxias 74
C10.228.854 Spinal Cord Diseases 310
C10.228.854.468 Muscular Atrophy, Spinal 129
C10.228.854.525 Myelitis 50
C10.228.854.583 Pneumorrhachis 1
C10.228.854.761 Spinal Cord Compression 226
C10.228.854.763 Spinal Cord Injuries 818
C10.228.854.765 Spinal Cord Neoplasms 112
C10.228.854.787.200 Friedreich Ataxia 54
C10.228.854.787.750 Olivopontocerebellar Atrophies 21
C10.228.854.787.875 Spinocerebellar Ataxias 74
C10.228.854.790 Stiff-Person Syndrome 14
C10.228.854.833 Syringomyelia 56
C10.228.854.889 Tabes Dorsalis 19
C10.574.500.024 Alexander Disease 6
C10.574.500.300 Canavan Disease 9
C10.574.500.362 Cockayne Syndrome 4
C10.574.500.497 Huntington Disease 322
C10.574.500.529 Lafora Disease 1
C10.574.500.545 Myotonia Congenita 17
C10.574.500.547 Myotonic Dystrophy 94
C10.574.500.549 Neurofibromatoses 28
C10.574.500.825.200 Friedreich Ataxia 54
C10.574.500.825.650 Olivopontocerebellar Atrophies 21
C10.574.500.825.700 Spinocerebellar Ataxias 74
C10.574.500.850 Tourette Syndrome 86
C10.574.500.865 Tuberous Sclerosis 141
C16.320.400.024 Alexander Disease 6
C16.320.400.150 Canavan Disease 9
C16.320.400.200 Cockayne Syndrome 4
C16.320.400.430 Huntington Disease 322
C16.320.400.480 Lafora Disease 1
C16.320.400.540 Myotonia Congenita 17
C16.320.400.542 Myotonic Dystrophy 94
C16.320.400.550 Neuroacanthocytosis 6
C16.320.400.560 Neurofibromatoses 28
C16.320.400.780.200 Friedreich Ataxia 54
C16.320.400.780.750 Olivopontocerebellar Atrophies 21
C16.320.400.780.875 Spinocerebellar Ataxias 74
C16.320.400.820 Tourette Syndrome 86
C16.320.400.880 Tuberous Sclerosis 141

Corneal cerebellar syndrome Disease MeSH Browser

Growth Failure, Microcephaly, Mental Retardation, Cataracts, Large Joint Contractures, Osteoporosis, Cortical Dysplasia, and Cerebellar Atrophy Disease MeSH Browser

Infantile onset spinocerebellar ataxia Disease MeSH Browser

Mousa Al din Al Nassar syndrome Disease MeSH Browser

Posterior column ataxia Disease MeSH Browser

Sensorimotor neuropathy with ataxia, autosomal dominant Disease MeSH Browser

Spinocerebellar Ataxia 29 Disease MeSH Browser

Spinocerebellar Ataxia, Autosomal Recessive 2 Disease MeSH Browser

Spinocerebellar ataxia 19 Disease MeSH Browser

Spinocerebellar ataxia 21 Disease MeSH Browser

Spinocerebellar ataxia 22 Disease MeSH Browser

Spinocerebellar ataxia 23 Disease MeSH Browser

Spinocerebellar ataxia 27 Disease MeSH Browser

Spinocerebellar ataxia 8 Disease MeSH Browser

Spinocerebellar ataxia, X-linked, 2 Disease MeSH Browser

Spinocerebellar ataxia, X-linked, 4 Disease MeSH Browser

Spinocerebellar ataxia, autosomal recessive 3 Disease MeSH Browser

Spinocerebellar ataxia, autosomal recessive 4 Disease MeSH Browser

Spinocerebellar ataxia, autosomal recessive 5 Disease MeSH Browser

Spinocerebellar ataxia, autosomal recessive 6 Disease MeSH Browser

Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy Disease MeSH Browser