spinocerebellar ataxia type 1
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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spinocerebellar ataxia type 1
Summary
spinocerebellar ataxia type 1 is a developmental defect during embryogenesis[1].
Key Facts
- spinocerebellar ataxia type 1's instance of is recorded as developmental defect during embryogenesis[2].
- spinocerebellar ataxia type 1's instance of is recorded as rare disease[3].
- spinocerebellar ataxia type 1's instance of is recorded as class of disease[4].
- spinocerebellar ataxia type 1 is a type of spinocerebellar ataxia[5].
- spinocerebellar ataxia type 1 is a type of Huntington's disease-like syndrome[6].
- spinocerebellar ataxia type 1 is a type of autosomal dominant cerebellar ataxia type I[7].
- spinocerebellar ataxia type 1's NCI Thesaurus ID is recorded as C129982[8].
- spinocerebellar ataxia type 1's genetic association is recorded as ATXN1[9].
- spinocerebellar ataxia type 1's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050954[10].
- spinocerebellar ataxia type 1's exact match is recorded as http://identifiers.org/doid/DOID:0050954[11].
- spinocerebellar ataxia type 1's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_98755[12].
- spinocerebellar ataxia type 1's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].