spinocerebellar ataxia type 20
Spinocerebellar ataxia type 20 (SCA20) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I; see this term). It is characterized by cerebellar dysarthria as the initial typical manifestation.
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spinocerebellar ataxia type 20
Summary
spinocerebellar ataxia type 20 is a developmental defect during embryogenesis[1].
Key Facts
- spinocerebellar ataxia type 20's instance of is recorded as developmental defect during embryogenesis[2].
- spinocerebellar ataxia type 20's instance of is recorded as class of disease[3].
- spinocerebellar ataxia type 20 is a type of spinocerebellar ataxia[4].
- spinocerebellar ataxia type 20 is a type of autosomal dominant cerebellar ataxia type I[5].
- spinocerebellar ataxia type 20's genetic association is recorded as DAGLA[6].
- spinocerebellar ataxia type 20's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050971[7].
- spinocerebellar ataxia type 20's exact match is recorded as http://identifiers.org/doid/DOID:0050971[8].
- spinocerebellar ataxia type 20's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_101110[9].
- spinocerebellar ataxia type 20's on focus list of Wikimedia project is recorded as WikiProject Medicine[10].