spinocerebellar ataxia type 1
(Q21097855)
Spinocerebellar ataxia type 1 (SCA1) is a subtype of type I autosomal dominant cerebellar ataxia (ADCA type I; see this term) characterized by dysarthria, writing difficulties, limb ataxia, and commonly nystagmus and saccadic abnormalities
Spinocerebellar ataxia type 1 (SCA1) is a subtype of type I autosomal dominant cerebellar ataxia (ADCA type I; see this term) characterized by dysarthria, writing difficulties, limb ataxia, and commonly nystagmus and saccadic abnormalities
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Current Data About
spinocerebellar ataxia type 1
(P31) |
(Q55788864)
(Q929833) (Q112193867) |
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(P279) |
(Q899726)
(Q24977062)
(Q55346087)
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(P1748) |
C129982
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(P2293) |
(Q14905515)
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(P2888) |
http://purl.obolibrary.org/obo/DOID_0050954
http://identifiers.org/doid/DOID:0050954
http://www.orpha.net/ORDO/Orphanet_98755 |
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(P5008) |
(Q4099686)
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other details
aliases |
Olivopontocerebellar Atrophy 1 SCA1 Spinocerebellar Ataxia type 1 SPINOCEREBELLAR ATAXIA 1; SCA1 Olivopontocerebellar Atrophy 4 SPINOCEREBELLAR ATAXIA 1 Spinocerebellar Atrophy 1 Schut-Haymaker Type Opca Menzel Type Opca Cerebelloparenchymal Disorder 1 |
description | Spinocerebellar ataxia type 1 (SCA1) is a subtype of type I autosomal dominant cerebellar ataxia (ADCA type I; see this term) characterized by dysarthria, writing difficulties, limb ataxia, and commonly nystagmus and saccadic abnormalities |
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