Spinocerebellar Ataxias [spinocerebelární ataxie]
- Terms
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autozomálně dominantní cerebelární ataxie typ 2
autozomálně dominantní cerebelární ataxie typ II
spinocerebelární ataxie typ 1
spinocerebelární ataxie typ 2
spinocerebelární ataxie typ 4
spinocerebelární ataxie typ 5
spinocerebelární ataxie typ 6
spinocerebelární ataxie typ 7
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Autosomal Dominant Cerebellar Ataxia, Type II
Cerebellar Degeneration with Slow Eye Movements
Cerebelloparenchymal Disorder I
Dominantly-Inherited Spinocerebellar Ataxias
Menzel Type OPCA
Olivopontocerebellar Atrophy 2
Olivopontocerebellar Atrophy I
Olivopontocerebellar Atrophy II
Olivopontocerebellar Atrophy III
Olivopontocerebellar Atrophy IV
Olivopontocerebellar Atrophy, Holguin Type
OPCA with Macular Degeneration and External Ophthalmoplegia
OPCA with Retinal Degeneration
SCA1
Schut-Haymaker Type OPCA
Spinocerebellar Ataxia 1
Spinocerebellar Ataxia 2
Spinocerebellar Ataxia 4
Spinocerebellar Ataxia 5
Spinocerebellar Ataxia 6
Spinocerebellar Ataxia 7
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 Ataxia with Slow Eye Movements
Spinocerebellar Ataxia-1
Spinocerebellar Ataxia-2
Spinocerebellar Ataxia-4
Spinocerebellar Ataxia-5
Spinocerebellar Ataxia-6
Spinocerebellar Ataxia-7
Spinocerebellar Ataxia, Autosomal Dominant, with Sensory Axonal Neuropathy
Spinocerebellar Ataxia, Cuban Type
Spinocerebellar Ataxias, Dominantly-Inherited
Spinocerebellar Atrophies
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
A group of 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)
- Annotation
- SPINOCEREBELLAR ATAXIA TYPE 3 see MACHADO-JOSEPH DISEASE is available
- DUI
- D020754 MeSH Browser
- CUI
- M0020337
- Previous indexing
- Ataxia/genetics (1965-1999); Cerebellar Diseases (1966-1999); Spinal Cord Diseases (1966-1999); Spinocerebellar Degenerations (1987-1999)
- History note
- 2000; use SPINOCEREBELLAR DEGENERATION 1987-1999
- Public note
- 2000; see SPINOCEREBELLAR DEGENERATION 1987-1999
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification 12
- CO
- complications 2
- CN
- congenital 2
- DI
- diagnosis 38
- DG
- diagnostic imaging 2
- DH
- diet therapy
- DT
- drug therapy 1
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology 4
- EH
- ethnology
- ET
- etiology 11
- GE
- genetics 36
- HI
- history
- IM
- immunology
- ME
- metabolism 2
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology 8
- PP
- physiopathology 11
- PC
- prevention & control
- PX
- psychology 3
- RT
- radiotherapy
- RH
- rehabilitation 2
- SU
- surgery
- TH
- therapy 12
- UR
- urine
- VE
- veterinary
- VI
- virology
Anemia, sideroblastic spinocerebellar ataxia Disease MeSH Browser
Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism Disease MeSH Browser
Gemignani syndrome Disease MeSH Browser
Spastic Ataxia Disease MeSH Browser
Spinocerebellar Ataxia 10 Disease MeSH Browser
Spinocerebellar Ataxia 11 Disease MeSH Browser
Spinocerebellar Ataxia 12 Disease MeSH Browser
Spinocerebellar Ataxia 15 Disease MeSH Browser
Spinocerebellar Ataxia 17 Disease MeSH Browser
Spinocerebellar Ataxia 31 Disease MeSH Browser
Spinocerebellar Ataxia With Rigidity And Peripheral Neuropathy Disease MeSH Browser
Spinocerebellar Ataxia with Dysmorphism Disease MeSH Browser
Spinocerebellar Ataxia with Epilepsy Disease MeSH Browser
Spinocerebellar Ataxia, Autosomal Recessive 7 Disease MeSH Browser
Spinocerebellar Ataxia, Autosomal Recessive 8 Disease MeSH Browser
Spinocerebellar Ataxia, X-Linked 1 Disease MeSH Browser
Spinocerebellar Ataxia, X-Linked 5 Disease MeSH Browser
Spinocerebellar ataxia 14 Disease MeSH Browser
Spinocerebellar ataxia 20 Disease MeSH Browser
Spinocerebellar ataxia 25 Disease MeSH Browser
Spinocerebellar ataxia 26 Disease MeSH Browser
Spinocerebellar ataxia 30 Disease MeSH Browser