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's subclass of is recorded as spinocerebellar ataxia[4].
- spinocerebellar ataxia type 20's subclass of is recorded as autosomal dominant cerebellar ataxia type I[5].
- spinocerebellar ataxia type 20's MeSH descriptor ID is recorded as C537199[6].
- spinocerebellar ataxia type 20's OMIM ID is recorded as 608687[7].
- spinocerebellar ataxia type 20's Disease Ontology ID is recorded as DOID:0050971[8].
- spinocerebellar ataxia type 20's Orphanet ID is recorded as 101110[9].
- spinocerebellar ataxia type 20's genetic association is recorded as DAGLA[10].
- spinocerebellar ataxia type 20's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050971[11].
- spinocerebellar ataxia type 20's exact match is recorded as http://identifiers.org/doid/DOID:0050971[12].
- spinocerebellar ataxia type 20's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_101110[13].
- spinocerebellar ataxia type 20's UMLS CUI is recorded as C1837541[14].
- spinocerebellar ataxia type 20's ICD-10-CM is recorded as G11.2[15].
- spinocerebellar ataxia type 20's GARD rare disease ID is recorded as 9997[16].
- spinocerebellar ataxia type 20's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
- spinocerebellar ataxia type 20's Mondo ID is recorded as MONDO_0012098[18].
- spinocerebellar ataxia type 20's UniProt disease ID is recorded as DI-03078[19].